Abstracts of the 37th Annual Meeting of the Society of Neuropediatrics

Abels, C

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl

Adler, C

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Agaimy, A

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Ahting, U

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Aktas, M

MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy

Alber, M

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Alberg, E

SelenoproteinN1-related myopathy: From clinical signs to diagnosis

Albrecht, U

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Antonius-Kluger, E

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Aslami, B

Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders

Axer, S

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Backes, H

Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders

Baethmann, M

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Banwell, B

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Barkmann, C

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Bar-Or, A

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Basheer, N

High incidence of paediatric CNS demyelination in East London

Bast, T

Modified Atkins diet as a treatment of epilepsy in 23 children

Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas

Resective surgery for refractory epilepsy in children under 4 years of age

Efficacy and safety of oral lacosamide as adjunctive therapy in children under 16 years with partial-onset seizures

Bauer, A

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Bauer, J

Neurocognitive deficits in children requiring heart transplantation during infancy

Bauer, M

PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome

Baumann, M

Suspected bromide intoxication due to ketogenic diet?

Baumann, U

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Baumgartner-Sigl, S

Suspected bromide intoxication due to ketogenic diet?

Bechtold-Dalla Pozza, S

Vitamin D levels in pediatric Multiple Sclerosis patients

Beck, J

A vanishing cerebellar tumor – too good to be true

Beck, M

The new Gaucher-Pass: A key tool in management of shortage

Becker, H

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Behnke-Hall, K

Neurocognitive deficits in children requiring heart transplantation during infancy

Behrends, U

Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox

Behrens, A

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Benninger, F

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Bentele, KHP

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Berger, A

A case of familial Labrune syndrome

Berger, C

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Bernhard, M

Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation

Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome

Bernhard, MK

TENS therapy in tension headaches – little helps much?!

Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies

Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Bernius, P

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Bertsche, A

Modification of epileptiform activity by blocking glial glutamate uptake

Berweck, S

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Betz, N

Modified Atkins diet as a treatment of epilepsy in 23 children

Bevot, A

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results

Beyerlein, A

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Bigi, S

Acquired isolated focal cerebellar lesions during development: effect on cognition?

Biskup, S

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Biste, M

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Bittner, R

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Blank, AE

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Blank, R

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Blankenburg, U

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Blaschek, A

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system

Vitamin D levels in pediatric Multiple Sclerosis patients

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Bluemcke, I

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Blümcke, I

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Bodamer, O

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Bode, H

Cerebral palsy: Predictors of psychosocial development

Böhmer, J

Migraine – the chameleon of diseases

Bohring, A

Potocki-Shaffer Syndrome: A case study

Boltshauser, E

Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?

Acquired isolated focal cerebellar lesions during development: effect on cognition?

Postnatal in-vivo MRI findings in anencephaly

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

Boor, R

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Borggraefe, I

Online EEG analysis by an epilepsy center

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

Borggräfe, I

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

Brackmann, F

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Brandl, U

The role of sharp wave activity in the consolidation of learning during sleep

Brandt, A

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Brassel, F

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Brehm, M

Cognitve impairment as a leading symptom in juvenile MS – two case reports -

Breithaupt, C

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Breiting, M

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Breuer, U

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Brilot, F

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Brix, O

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Brixius-Huth, M

The new Gaucher-Pass: A key tool in management of shortage

Brocke, K

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Bruehl, C

Modification of epileptiform activity by blocking glial glutamate uptake

Brunner-Krainz, M

Multiple arteriovenous malformations of the brain: A case report

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Büchel, A

Optic nerve sheath diameter by ultrasound in children and adolescents with headache

Buchmann, A

Morphometric MRI findings in adolescents with congenital heart disease

Bültmann, E

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Burdach, S

Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Burtzlaff, C

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)

Stiff-persons syndrome in a 12 year old child – a case report

Busse, M

Ataxia telangiectasia in dizygotic two year old twins

Bussmann, CB

Oculocutaneous albinism

Bußmann, C

PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome

Christen, HJ

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Clas, P

Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images

Coppola, G

First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Crow, YJ

A case of familial Labrune syndrome

Csaicsich, D

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Czermin, B

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Dahlin, M

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Dale, RC

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Danhauser, K

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Das, AM

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Dechant, K

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Deiters, L

Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales

Delalande, O

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

de Lonlay, P

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Delvendahl, I

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Denecke, J

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

Familial occurence of congenital bilateral perisylvian syndrom

Deppe, W

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Derfuß, T

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

der Hagen, M von

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Diepold, K

Late-onset folinic acid-responsive seizures

Dikow, N

Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly

Distelmaier, F

How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey

Dornmair, K

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Draguhn, A

Modification of epileptiform activity by blocking glial glutamate uptake

Dressel, P

Neurological presentations in children with serological active mycoplasma pneumoniae infection

Dressler, A

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Eberhard, C

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Ebner, A

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Ebner, K

Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?

Eder, HG

Multiple arteriovenous malformations of the brain: A case report

Eisenhofer, G

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

Eitel, H

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Eitel, HC

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Elger, CE

A method for automated volumetry to assess disease progression in Rasmussen Encephalitis

Elix, H

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Elsenbruch, S

Health- related quality of life in patients with Duchenne Muscular Dystrophy

Elstner, M

Identification of a second major locus for neurodegeneration with brain iron accumulation

Engelsberger, I

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Ensslen, M

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

Eves, K

The treatment of young children with low trunkal tone, as a result of various diagnoses, with dynamic GPS Soft Orthoses – case studies

Faber, J

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Feldkamp, A

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Feucht, M

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Fiedler, B

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl

Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene

Fiedler, BJ

Potocki-Shaffer Syndrome: A case study

Finetti, C

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Fingerhut, M

Status epilepticus in a newborn – pyridoxine toxicity?

Fleischer, J

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Flössel, U

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Forne, I

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Fowler, B

Infantile epileptic encephalopathy due to cobalamin deficiency?

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Franke, C

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Frauenknecht, K

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Freilinger, M

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Freisinger, P

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Freudenberg, L

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Gabriel, H

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Gangfuß, A

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Garkisch, S

PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism

Gärtner, J

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Gassmann, M

Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain

Gebhardt, B

Optic nerve sheath diameter by ultrasound in children and adolescents with headache

Geers, B

Health- related quality of life in patients with Duchenne Muscular Dystrophy

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Geiger, K

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Geis, T

An unusual tremor

A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding

Gencik, M

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Gerleve, H

The effect of Lamotrigin and Levetiracetam on the perinatal period

Encephalitis of varizella-zoster in a 26 months old child

Gerstner, T

Resective surgery for refractory epilepsy in children under 4 years of age

Getzinger, T

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Geuze, R

AWMF-Guideline developmental coodination disorder: definition and assessment

Goeggel Simonetti, B

A vanishing cerebellar tumor – too good to be true

Gold, R

Optical Coherence Tomography in neuro-pediatric diseases – A case report

Goll, A

Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results

Grohmann, K

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)

Gröschel, S

Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Grossmann, R

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

Gruber-Sedlmayr, U

Multiple arteriovenous malformations of the brain: A case report

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Gushahn, L

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Haack, T

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Identification of a second major locus for neurodegeneration with brain iron accumulation

Haack, TB

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Habelt, C

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Haberberger, B

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Haberlandt, E

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Suspected bromide intoxication due to ketogenic diet?

Häberle, J

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Haffner, D

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

Familial occurence of congenital bilateral perisylvian syndrom

Hahn, A

PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism

Neurocognitive deficits in children requiring heart transplantation during infancy

Postanoxic myoclonus (Lance-Adams syndrome) after near-drowning

Hannibal, I

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

Hans, V

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Harter, PN

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Hartig, MB

Identification of a second major locus for neurodegeneration with brain iron accumulation

Härtig, W

Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever

Hartlieb, T

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Hartmann, H

Status epilepticus in a newborn – pyridoxine toxicity?

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Hartmann, M

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Hasilik, M

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Hauffa, B

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Haug, V

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Hauser, TK

Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?

Häusler, M

MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy

Rufinamide. A new therapeutic option for epilepsy with myoclonic absences

Heidrich, A

The new Gaucher-Pass: A key tool in management of shortage

Heim, K

Identification of a second major locus for neurodegeneration with brain iron accumulation

Heinen, F

Online EEG analysis by an epilepsy center

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Abstracts of the 37th Annual Meeting of the Society of – Neuropediatrics, „Gesellschaft für Neuropädiatrie“ – 7nd to 10th April 2011

Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system

Vitamin D levels in pediatric Multiple Sclerosis patients

Heiniger, U

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Heinks-Maldonado, T

Acquired isolated focal cerebellar lesions during development: effect on cognition?

Heinrich, M

Familiarity and course of specific language impairment of 175 children

Heinrich, T

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Hemmer, B

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Hempel, M

Familiarity and course of specific language impairment of 175 children

Identification of a second major locus for neurodegeneration with brain iron accumulation

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Henrich, M

Ataxia telangiectasia in dizygotic two year old twins

Herberhold, TM

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Herraiz Rocamora, J

Inv dup (15) syndrome and refractory epilepsy: A case-report

Hessel, A

Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results

Hessenauer, M

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report

Heußinger, N

Isolated optic neuritis is associated with development of pediatric multiple sclerosis

Hiener, U

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Himpel, M

TENS therapy in tension headaches – little helps much?!

Hinterstoißer, K

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Hinz, AB

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Hirsch, W

Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Hirzinger, M

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Hoffmann, GF

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Hofmann, W

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Hohlfeld, R

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Holert, N

Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report

Holinski-Feder, E

Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene

Holthausen, H

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Homburg, MC

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

Honnef, D

MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy

Hoppen, T

Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis

Hörster, F

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Horvat, R

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Horvath, R

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Hoser, J

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Huber, R

Qualitative and quantitative motor performance in adolescents with CHD

Hübner, A

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Huisman, TAGM

Postnatal in-vivo MRI findings in anencephaly

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

Hume, R

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

Hung, C

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Huppke, P

Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis

Huß, K

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Hütsch, C

Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results

Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study

Illsinger, S

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Iuso, A

Identification of a second major locus for neurodegeneration with brain iron accumulation

Jacob, U

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Jakobs, C

Status epilepticus in a newborn – pyridoxine toxicity?

Janello, C

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

Janetschek, C

Suspected bromide intoxication due to ketogenic diet?

Jansen, C

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Jenne, D

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Jenni, O

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Jozwiak, S

Identification of a second major locus for neurodegeneration with brain iron accumulation

Jung, N

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Jung, NH

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Jurkiewicz, E

Identification of a second major locus for neurodegeneration with brain iron accumulation

Kalbhenn, T

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Kalle, T von

Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood

Kalmus, U

The effect of Lamotrigin and Levetiracetam on the perinatal period

Stimulus-sensitive epilepsy, with seizures while feeding in the morning

Encephalitis of varizella-zoster in a 26 months old child

Käppeli, M

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Karall, D

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Suspected bromide intoxication due to ketogenic diet?

Karch, S

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly

Karenfort, M

Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse

Crossed cerebellar diaschisis after status epilepticus

Karlmeier, A

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Keimer, R

Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood

Kennerknecht, I

Hereditary prosopagnosia

Kessler, S

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Kessler-Uberti, S

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

Keßler-Uberti, S

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Keßner, R

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Khademi, M

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Kiechl-Kohlendorfer, U

Old and new antiepileptic drugs during pregnancy and lactation – report of a case

Kiefer, A

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Kiess, W

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Kilian, D

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Kirchhoff, F

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

Kirsch, S

Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood

Kissenbeck, C

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Klaver, P

Qualitative and quantitative motor performance in adolescents with CHD

Morphometric MRI findings in adolescents with congenital heart disease

Klee, D

Crossed cerebellar diaschisis after status epilepticus

Klein, C

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Klein, GE

Multiple arteriovenous malformations of the brain: A case report

Klepper, J

20 years of GLUT1 Deficiency: where are we today?

Klopstock, T

Identification of a second major locus for neurodegeneration with brain iron accumulation

Kluger, G

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Rufinamide. A new therapeutic option for epilepsy with myoclonic absences

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Kmiec, T

Identification of a second major locus for neurodegeneration with brain iron accumulation

Knirsch, W

Morphometric MRI findings in adolescents with congenital heart disease

Koch, J

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Koch, K

Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly

Koch, KA

Oculocutaneous albinism

Koehler, T

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Koeller, DM

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Kohleis, K

Cerebral palsy: Predictors of psychosocial development

Köhler, C

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Kohlhase, J

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Kohlschütter, A

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Kölker, S

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Kolodziejczyk, D

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Korenke, GC

Congenital mirror movements in a family with a novel mutation in the DCC gene

Korinthenberg, R

Infantile epileptic encephalopathy due to cobalamin deficiency?

Resective surgery for refractory epilepsy in children under 4 years of age

Cognitve impairment as a leading symptom in juvenile MS – two case reports -

Kotzaeridou, U

PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome

Kovacevic-Preradovic, T

Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report

Koy, A

Crossed cerebellar diaschisis after status epilepticus

Krägeloh-Mann, I

Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results

Krajewska-Walasek, M

Identification of a second major locus for neurodegeneration with brain iron accumulation

Kraus, V

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Neurological presentations in children with serological active mycoplasma pneumoniae infection

Kress, W

A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding

SelenoproteinN1-related myopathy: From clinical signs to diagnosis

Kretzschmar, H

Identification of a second major locus for neurodegeneration with brain iron accumulation

Kries, R von

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Kroisl, P

Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report

Kröpfl, T

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Krumbholz, M

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Kudernatsch, M

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Kujat, A

Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies

Kull-Sadacharam, K

Sensory – Integrative Ayres Therapie SIAT® – www.gsid.de

Kumar, V

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Kummer, S

How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey

Kümpfel, T

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Kurlemann, G

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl

Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene

Potocki-Shaffer Syndrome: A case study

Kutsche, K

Congenital mirror movements in a family with a novel mutation in the DCC gene

Kutschke, G

A case of familial Labrune syndrome

Laage-Gaupp, A

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Lämmer, C

Repeated bilateral dystonic elevation of visual gaze in a 15-year-old girl

Lanator, I

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Lange-Hüsken, F

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Langhagen, T

Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system

Vitamin D levels in pediatric Multiple Sclerosis patients

Latal, B

Qualitative and quantitative motor performance in adolescents with CHD

Morphometric MRI findings in adolescents with congenital heart disease

Lauffer, H

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)

Stiff-persons syndrome in a 12 year old child – a case report

Leis, T

Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales

Leiz, S

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Lengnick, K

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Lidzba, K

Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?

Linder-Lucht, M

Inv dup (15) syndrome and refractory epilepsy: A case-report

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Lippert, M

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Logeswaran, T

Neurocognitive deficits in children requiring heart transplantation during infancy

Lotte, J

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

Louwen, F

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Lübbig, A

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

Lücke, T

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Optical Coherence Tomography in neuro-pediatric diseases – A case report

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Lüdtke, U

Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis

Luef, G

Old and new antiepileptic drugs during pregnancy and lactation – report of a case

Lutz, S

Ataxia telangiectasia in dizygotic two year old twins

A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding

SelenoproteinN1-related myopathy: From clinical signs to diagnosis

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy

Maak, A

Congenital mirror movements in a family with a novel mutation in the DCC gene

Madignier, F

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Magalhaes, S

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Mainberger, F

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Makowski, C

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Neurological presentations in children with serological active mycoplasma pneumoniae infection

Longitudinally very extensive acute transverse myelitis after influenza vaccination

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Mall, V

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries

Cognitve impairment as a leading symptom in juvenile MS – two case reports -

Manero Borràs, RM

Inv dup (15) syndrome and refractory epilepsy: A case-report

Marquard, K

Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood

Marquardt, T

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Marschall, C

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Martinez, A

High incidence of paediatric CNS demyelination in East London

Mayatepek, E

How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey

Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse

Crossed cerebellar diaschisis after status epilepticus

Mayer, H

Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas

Mayer, T

Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report

Mayr, J

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Mayr, JA

Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome

Meinl, E

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Meitinger, T

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Familiarity and course of specific language impairment of 175 children

Identification of a second major locus for neurodegeneration with brain iron accumulation

Mengel, E

The new Gaucher-Pass: A key tool in management of shortage

Meoded, A

Postnatal in-vivo MRI findings in anencephaly

Merkenschlager, A

Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation

TENS therapy in tension headaches – little helps much?!

Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies

Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever

Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Mettin, RR

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Meyer, H

Resective surgery for refractory epilepsy in children under 4 years of age

Meyer, S

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Michaelis, U

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries

Mirjam, L

TENS therapy in tension headaches – little helps much?!

Mittelbronn, M

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Moog, U

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly

Mörzinger, M

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Mueller-Felber, W

Identification of a second major locus for neurodegeneration with brain iron accumulation

Mühlebner, A

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Müller, A

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Müller-Felber, W

Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system

Vitamin D levels in pediatric Multiple Sclerosis patients

Munteanu, M

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Nagel, A

Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results

Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study

Narayanan, U

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Nauer, C

A vanishing cerebellar tumor – too good to be true

Navah, F

Resective surgery for refractory epilepsy in children under 4 years of age

Neidhardt, K

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Neubauer, BA

PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism

Neurocognitive deficits in children requiring heart transplantation during infancy

Postanoxic myoclonus (Lance-Adams syndrome) after near-drowning

Ney, S

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Niemeyer, T

Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results

Nikanorova, M

Rufinamide. A new therapeutic option for epilepsy with myoclonic absences

Nögel, SC

Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales

Nolte-Buchholtz, S

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Noss, J

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Nüßlein, T

Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis

Oexle, K

Identification of a second major locus for neurodegeneration with brain iron accumulation

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Oh, J

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Okun, JG

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Olsson, I

Migraine – the chameleon of diseases

Olsson, T

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Olze, A

Efficacy and safety of oral lacosamide as adjunctive therapy in children under 16 years with partial-onset seizures

Opladen, T

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Opp, S

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Pahs, G

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Pannek, HW

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Pascher, B

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Penzien, J

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

Pereira, B

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Peters, J

Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy

Pfister, ED

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Pfurtscheller, K

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Philippi, H

Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders

Pieper, T

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Pietz, J

Modification of epileptiform activity by blocking glial glutamate uptake

PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly

Plecko, B

Status epilepticus in a newborn – pyridoxine toxicity?

Multiple arteriovenous malformations of the brain: A case report

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report

Pletziger, E

Encephalitis of varizella-zoster in a 26 months old child

Plümpe, N

Hereditary prosopagnosia

Pohl, D

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Pöhler, V

PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism

Polatajko, H

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Polster, T

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Poretti, A

Postnatal in-vivo MRI findings in anencephaly

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

Poths, S

Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders

Preisler, B

The treatment of young children with low trunkal tone, as a result of various diagnoses, with dynamic GPS Soft Orthoses – case studies

Pröbstel, AK

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Prokisch, H

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Identification of a second major locus for neurodegeneration with brain iron accumulation

Prothmann, A

Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Pyper, A

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Raabe, C

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Ramantani, G

Resective surgery for refractory epilepsy in children under 4 years of age

Rauchenzauner, M

Old and new antiepileptic drugs during pregnancy and lactation – report of a case

Rauscher, C

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Reihle, C

Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood

Reinke, J

The new Gaucher-Pass: A key tool in management of shortage

Reiserer, B

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Reiter-Fink, E

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Reithofer, E

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Reitter, A

Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?

Reitter, B

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

A case of familial Labrune syndrome

Reutlinger, C

Successful treatment of parainfectious encephalitis with ivIG in a boy with FraX

Rhein, M von

The new Gaucher-Pass: A key tool in management of shortage

Qualitative and quantitative motor performance in adolescents with CHD

Morphometric MRI findings in adolescents with congenital heart disease

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Richterich, A

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Richwien, R

Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders

Rienhardt, C von

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Ries, M

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Rivera-Brugués, N

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Robl, H

Online EEG analysis by an epilepsy center

Rocamora Zúñiga, R

Inv dup (15) syndrome and refractory epilepsy: A case-report

Roeber, S

Identification of a second major locus for neurodegeneration with brain iron accumulation

Roland-Schäfer, D

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Rolinski, B

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Roloff-Messing, V

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Romein, E

Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Roquer González, J

Inv dup (15) syndrome and refractory epilepsy: A case-report

Rosenbaum, T

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Hereditary prosopagnosia

Rosenberger, G

Congenital mirror movements in a family with a novel mutation in the DCC gene

Rostasy, K

Old and new antiepileptic drugs during pregnancy and lactation – report of a case

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Rostásy, K

Suspected bromide intoxication due to ketogenic diet?

Rötzer, K

Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report

Rufino, A

Migraine – the chameleon of diseases

Rülander, C

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case

Rutsch, F

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl

Sandrieser, T

Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis

Sauer, SW

Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I

Saur, V

Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy

Schaaf, K

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Schaefer, C

Qualitative and quantitative motor performance in adolescents with CHD

Schäfer, J

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Schäfer, JS

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

Schallner, J

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

Schara, U

Health- related quality of life in patients with Duchenne Muscular Dystrophy

Ataxia telangiectasia in dizygotic two year old twins

An unusual tremor

A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding

SelenoproteinN1-related myopathy: From clinical signs to diagnosis

Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)

Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy

Schauer, U

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Scheer, I

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

Scheffner, T

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Schiegl, H

Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?

Schilling, M

The role of sharp wave activity in the consolidation of learning during sleep

Schimmel, M

Suspected bromide intoxication due to ketogenic diet?

Schmid, J

Health- related quality of life in patients with Duchenne Muscular Dystrophy

Schmidt, T

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Schmook, MT

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Schneider, C

Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain

Schneider, HC

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Schoemaker, M

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Schoene-Bake, JC

A method for automated volumetry to assess disease progression in Rasmussen Encephalitis

Scholl-Buergi, S

Suspected bromide intoxication due to ketogenic diet?

Scholl-Bürgi, S

Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol

Schönfelder, J

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Schröder, AS

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept

The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study

Schröder, C

Stiff-persons syndrome in a 12 year old child – a case report

Schröder, SA

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

Schroeder, AS

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Schroeder, S

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Schubert, C

Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation

Schubert, S

Resective surgery for refractory epilepsy in children under 4 years of age

Schucht, P

A vanishing cerebellar tumor – too good to be true

Schugal, A

High incidence of paediatric CNS demyelination in East London

Schuhmann, M

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Schuhmann, MU

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Schulte-Markwort, M

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Schulz, A

Psychopathology in CLN3 disease: Correlation with disease progression and quality of life

Schulze-Bonhage, A

Resective surgery for refractory epilepsy in children under 4 years of age

Schuster, V

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Schwab, KO

Infantile epileptic encephalopathy due to cobalamin deficiency?

Schwahn, B

Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Schwerin-Nagel, A

Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report

Schwindt, W

Potocki-Shaffer Syndrome: A case study

Seidl, R

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Seidlitz, G

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)

Seitz, A

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Siebers-Renelt, U

Potocki-Shaffer Syndrome: A case study

Siegel, C

Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum

Sigler, C

Late-onset folinic acid-responsive seizures

Smitka, M

Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy

Smits-Engelsman, B

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Sömmer, J

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Sorantin, E

Multiple arteriovenous malformations of the brain: A case report

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients

Sperl, P

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Sperl, W

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome

Spescha, H

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Spiegler, J

Successful treatment of parainfectious encephalitis with ivIG in a boy with FraX

Sprinz, A

Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results

Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study

Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy

Stark, W

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Staudt, M

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Objective identification of successful performed clinical fMRI in children

Therapy of Hemiparesis in children and adolescents – a 5 years experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report

Stein, S

Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries

Steiner, F

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Steinlin, M

Acquired isolated focal cerebellar lesions during development: effect on cognition?

A vanishing cerebellar tumor – too good to be true

Stephani, U

Resective surgery for refractory epilepsy in children under 4 years of age

Sterl, E

Multiple arteriovenous malformations of the brain: A case report

Stevanowa, N

Familiarity and course of specific language impairment of 175 children

Storck, M

Cerebral palsy: Predictors of psychosocial development

Storm van's Gravesande, K

Cognitve impairment as a leading symptom in juvenile MS – two case reports -

Straube, A

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Striano, P

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

Strobl, K

Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas

Resective surgery for refractory epilepsy in children under 4 years of age

Stroet, A

Optical Coherence Tomography in neuro-pediatric diseases – A case report

Strom, TM

Identification of a second major locus for neurodegeneration with brain iron accumulation

Strotmann, P

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Neurological presentations in children with serological active mycoplasma pneumoniae infection

Strupp, M

Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system

Stülpnagel, C von

Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?

First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy

Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome

First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy

Syrbe, S

Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation

TENS therapy in tension headaches – little helps much?!

Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies

Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever

Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex

Tacke, UH

Infantile epileptic encephalopathy due to cobalamin deficiency?

Tantsis, E

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Tatagiba, M

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Tauer, U

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Tegetmeyer, H

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Teig, N

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Tesarova, M

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Thiele, S

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)

Stiff-persons syndrome in a 12 year old child – a case report

Thiels, C

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Thümmler, K

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Tibussek, D

How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey

Toelle, SP

Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?

Trantakis, C

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Triltsch-Ciurea, I

Familiarity and course of specific language impairment of 175 children

Trimmel-Schwahofer, P

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Trollmann, R

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation

Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain

Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales

Isolated optic neuritis is associated with development of pediatric multiple sclerosis

Tuxhorn, I

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Utz, N

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Utzig, N

Stiff-persons syndrome in a 12 year old child – a case report

Uziel, G

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Valls Santasusana, A

Inv dup (15) syndrome and refractory epilepsy: A case-report

Valsangiacomo, ER

Qualitative and quantitative motor performance in adolescents with CHD

van Velthofen, V

Resective surgery for refractory epilepsy in children under 4 years of age

Villalobos, A

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Vivanco Hidalgo, RM

Inv dup (15) syndrome and refractory epilepsy: A case-report

Wagner, J

A method for automated volumetry to assess disease progression in Rasmussen Encephalitis

Wagner, K

Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report

Wagner, M

Congenital mirror movements in a family with a novel mutation in the DCC gene

Wagner, O

Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening

Wahlländer-Danek, U

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Waibel, P

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Walkinshaw, G

Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain

Walsh, S

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

Familial occurence of congenital bilateral perisylvian syndrom

Warken, B

Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?

Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy

Weber, AA

Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse

Crossed cerebellar diaschisis after status epilepticus

Weber, B

A method for automated volumetry to assess disease progression in Rasmussen Encephalitis

Weber, F

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Weber-Sannwald, A

Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders

Weibel, L

Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?

Weigt-Usinger, K

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Optical Coherence Tomography in neuro-pediatric diseases – A case report

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Weimer, W

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl

Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene

Weir, S

CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort

Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results

Weiss, D

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

Familial occurence of congenital bilateral perisylvian syndrom

Weiss, K

Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy

Weissert, M

Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report

Weissert, R

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Weitkämper, A

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Wekerle, H

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Wenner, K

Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences

Wiegand, G

Resective surgery for refractory epilepsy in children under 4 years of age

Wiemer-Kruel, A

Modified Atkins diet as a treatment of epilepsy in 23 children

Wilke, M

Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images

Objective identification of successful performed clinical fMRI in children

Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?

Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor

Wilken, B

Late-onset folinic acid-responsive seizures

Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders

Wilson, P

AWMF-Guideline developmental coodination disorder: definition and assessment

AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention

Wingeier, K

Acquired isolated focal cerebellar lesions during development: effect on cognition?

Winkelmann, J

Identification of a second major locus for neurodegeneration with brain iron accumulation

Winkler, PA

Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions

Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection

Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome

Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients

Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion

"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis

Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy

12 years of pediatric epilepsy surgery – The Vogtareuth experience

Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results

Winkler, T

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Winkler, U

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Wintergerst, U

Online EEG analysis by an epilepsy center

Wittig, I

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Woermann, F

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009

Wolf, NI

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia

Wülker, N

Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results

Wüller, D

Encephalitis of varizella-zoster in a 26 months old child

Wüller, DH

The effect of Lamotrigin and Levetiracetam on the perinatal period

Wurm, RE

Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation

Zarits, P

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Zeder, SL

Multiple arteriovenous malformations of the brain: A case report

Zenker, M

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1

Zentner, J

Resective surgery for refractory epilepsy in children under 4 years of age

Zeviani, M

Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Zimmermann, F

Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy

Zsoter, A

Objective identification of successful performed clinical fMRI in children