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Abdul-Khaliq, H
The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease
Abels, C
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Narcolepsy in early childhood – a case study with video
First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood
Acquaviva, C
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Ae Lee-Kirsch, M
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Aksu, F
The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception
Alber, M
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis
Althaus, J
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Arnold, M
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Assmann, B
„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Auber, B
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
Axer, S
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Baethmann, M
Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation
Baldeweg, T
Microstructural alterations of motor pathways in adolescents born preterm
Baric, I
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Bast, T
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Bauer, MF
Novel Missence Mutation in the BCS1L Gene as a Cause of mitochondrial encephalopathy with Fanconi Syndrome
Bauer, O
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Bäumer, T
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Baz Bartels, M
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Bentele, KHP
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Berger, C
Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?
Bergmann, K
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Bertsche, A
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Bertsche, T
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Bevot, A
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Bien, CG
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis
Bigi, S
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Biscaldi-Schäfer, M
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Blankenburg, M
The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception
Blüthner, M
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Böckelman, S
Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse
Bockius, D
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Boltshauser, E
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Bönnemann, CG
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Boor, R
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Borusiak, P
MRI in children with epilepsy and hydrocephalus – the clinical relevance of improved techniques
Long-term outcome of Alice-in-Wonderland-Syndrome: Results from a case series of 12 patients
Böss, A
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Boy, SPN
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Brandl, A
Correlations between early stress experiences and later behavior regulation in premature born toddlers with low and very low birth weight at the age of two years
Brandl, U
ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome
Brandt, A
Impaired motor cortex plasticity in patients with Noonan syndrome
Brassel, F
The plexiform neurofibroma is an important differential diagnosis of congenital facial swelling
Braulke, T
High phenotype variability in CLN3 patients with identical genotype
Identification of potential biomarkers and modifiers of CLN3-disease progression
Breuer, K
Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation
Brocke, K
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Brockmann, K
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Polymicrogyria in Fetal Alcohol Syndrome
Brüggemann, N
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Brunner-Krainz, M
Infantile Alexander Disease mimicking multilocular astrocytoma
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Büchel, A
Promising treatment in a boy with creatine transporter deficiency
Bültmann, E
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Burgard, P
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Burger, W
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Bürki, S
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Christen, HJ
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Clarke, NF
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Classen, G
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Autosomal dominant nocturnal frontal lobe epilepsy in mother and daughter treated with an unusual combination of anticonvulsants
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience
Coker, M
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Connelly, A
Microstructural alterations of motor pathways in adolescents born preterm
Coropceanu, D
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Danz, B
Current practice in the management of newborns with spina bifida in Germany
Das, A
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Das, AM
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
de Brouwer, APM
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Deiters, L
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Preterm and small-for-gestational age: no risk for an adverse cognitive development?
Dekomien, G
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
Della Marina, A
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay
Delvendahl, I
Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation
Demir, Z
Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse
Denecke, J
Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation
Deppe, M
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
Deppe, W
Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?
Dercks, M
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results of a longitudinal study
der Hagen, M von
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
De Sonneville, L
Impairment of executive functions in pediatric posterior fossa tumor survivors
Dickhaus, H
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Diekmann, S
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
Ding, XQ
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Dinomais, M
Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Dittrich, S
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Döbler-Neumann, M
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Dossal, S
Long-term follow up of preterms below 33 weeks of gestation at school age
Drabsch, C
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Dreha-Kulaczewski, S
Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism
Dresel, R
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Driess, J
Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes
Dubeau, F
Dynamic analysis of absence seizures in humans: all the same but all different
Dümpelmann, M
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Ebinger, F
Novel Missence Mutation in the BCS1L Gene as a Cause of mitochondrial encephalopathy with Fanconi Syndrome
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Dronabinol for the treatment of unspecific pain, restlessness and spasticity in neuropaediatrics
Prevalence of headache in preschool children
Ehrich, JHH
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Eitel, H
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience
El-Koussy, M
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Engelke, UFH
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Ensenauer, R
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Enzinger, C
First manifestation and clinical course of eleven paediatric patients with Multiple Sclerosis assigned to the University Hospital of Children and Adolescents of the Medical University Graz from 2001 to 2009
Ernst, JP
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Feldkamp, A
The plexiform neurofibroma is an important differential diagnosis of congenital facial swelling
Ferreiro, A
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Fiedler, B
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
CK elevation and progressive toe walking in a 14-year old girl
Narcolepsy in early childhood – a case study with video
First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood
Finetti, C
Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?
The plexiform neurofibroma is an important differential diagnosis of congenital facial swelling
Fischer, U
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Fleischer, J
Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?
Fluss, J
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Freudenberg, L
Impaired motor cortex plasticity in patients with Noonan syndrome
Furtwängler, R
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Gad, D
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience
Gaertner, H
Prevalence of headache in preschool children
Gärtner, J
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism
Developmental retardation due to dietary vitamin B12 deficiency during infancy
Polymicrogyria in Fetal Alcohol Syndrome
Gburek-Augustat, J
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Geb, S
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Gebhardt, B
Promising treatment in a boy with creatine transporter deficiency
Gebhardt, U
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Impaired satiety regulation in obese patients with craniopharyngioma
Gegner, S
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Gerstner, T
Novel Missence Mutation in the BCS1L Gene as a Cause of mitochondrial encephalopathy with Fanconi Syndrome
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Ghiath Shamdeen, M
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Gissen, P
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Goebel, HH
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Gortner, L
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Gotman, J
Dynamic analysis of absence seizures in humans: all the same but all different
Gottschalk, A
Current practice in the management of newborns with spina bifida in Germany
Grapp, M
Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism
Grieben, U
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Grimm, T
CK elevation and progressive toe walking in a 14-year old girl
Grodd, W
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Gröschel, S
Microstructural alterations of motor pathways in adolescents born preterm
Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Gruber-Sedlmayr, U
First manifestation and clinical course of eleven paediatric patients with Multiple Sclerosis assigned to the University Hospital of Children and Adolescents of the Medical University Graz from 2001 to 2009
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Grünert, S
Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes
Haas, D
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Haas-Lude, K
Growth hormone treatment of patients with neurofibromatosis type 1
Hadders-Algra, M
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Haefeli, WE
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Haege, G
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Haffner, D
Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation
Hahn, A
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Singultus as main seizure type in a patient with primary generalized epilepsy
Hahn, G
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Hanisch, E
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Hanke, G
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Hannak, D
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Harting, I
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Hartmann, H
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Hartmann, K
Dronabinol for the treatment of unspecific pain, restlessness and spasticity in neuropaediatrics
Haschemi, M
The concept of modular motor therapy in paediatric neurology
Hasselmann, O
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Haud, N
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
Häusler, M
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Heales, S
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Hechler, T
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception
Heinen, F
Impaired motor cortex plasticity in patients with Noonan syndrome
Henneke, M
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
Henschen, M
Is the assessment of general movements helpful for the prediction of the neurodevelopmental outcome in a child with symptomatic congenital CMV infection?
Hentschel, R
Long-term follow up of preterms below 33 weeks of gestation at school age
Henze, G
Impairment of executive functions in pediatric posterior fossa tumor survivors
Heringer, J
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Hermann, E
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Hernáiz Driever, P
Impairment of executive functions in pediatric posterior fossa tumor survivors
Hertzberg, C
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Hessenauer, M
Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions
Heyer, C
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
Hiener, U
Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation
Hilbig, K
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience
Hoche, F
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Hoffmann, GF
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Hofmann-Peters, A
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Autosomal dominant nocturnal frontal lobe epilepsy in mother and daughter treated with an unusual combination of anticonvulsants
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience
Höger, C
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
Holinski-Feder, E
6q13–6q14.1 deletion syndrome characterized by congenital myopathy, mental retardation and minor dysmorphisms – a case report
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay
Holthausen, H
Asymmetrical localisation of the motor cortex after perinatally acquired intracerebral hemorrhage: Volume shift versus neuroplasticity
Hoppe-Tichy, T
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Horber, V
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Horváth, R
BARTH SYNDROME with a new mutation without cardial involvement
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Hoy, L
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Huber-Zeyringer, A
Urodynamic findings by routine preoperative assessment in 46 scoliotic patients
Hübner, A
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Huppke, B
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Huppke, P
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Developmental retardation due to dietary vitamin B12 deficiency during infancy
Hurlstone, A
RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder
Husain, R
ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome
i Dali, C
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Illsinger, S
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Innes, M
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Jacobs, J
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Jakobs, C
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Jansen, O
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Jardine, P
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Jeannet, PY
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Jenke, ACW
Long-term outcome of Alice-in-Wonderland-Syndrome: Results from a case series of 12 patients
Jung, N
Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation
Jung, T
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Junker, J
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Kalkan Ucar, S
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Kalmus, U
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Kämmerer, F
Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?
Kammler, G
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Kamrath, C
Hypothalamic and pituitary affection after traumatic brain injury in childhood
Karch, D
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Karlmeier, A
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience
Kehrer, C
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Keimer, R
Helmets or physiotherapy? Natural history and treatment options for non-synostotic skull deformity in children – results of a literature search
Neurofibromatosis type 1 (Recklinghausen's Disease). Who was Friedrich Daniel von Recklinghausen?
Kentouche, K
ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome
Kerber, K
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Kessler, S
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience
Kieslich, M
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Kilian, D
High phenotype variability in CLN3 patients with identical genotype
Kim, KS
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Kirschner, J
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
6q13–6q14.1 deletion syndrome characterized by congenital myopathy, mental retardation and minor dysmorphisms – a case report
Klein, C
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Klinge, L
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Kluger, G
Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions
Therapy-refractory symptomatic focal epilepsy with methylmalonic aciduria: Case report on positive effect of rufinamide
Kluijtmans, LAJ
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Knöppler, K
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Knuf, M
Postoperative outcome of children with neural tube defects and craniocervical decompression surgery: risk factors with regard to complications and length of hospitalisation
Koch, KA
Neuropathia vestibularis: a differential diagnosis of vertigo
Köhler, B
Neurofibromatosis type 1 (Recklinghausen's Disease). Who was Friedrich Daniel von Recklinghausen?
Köhler, C
BARTH SYNDROME with a new mutation without cardial involvement
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
Köhler, U
Application of Array-based Comparative Genome Hybridization in patients with mental retardation
Kohlhase, J
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Kohlschütter, A
High phenotype variability in CLN3 patients with identical genotype
Identification of potential biomarkers and modifiers of CLN3-disease progression
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Kolb, R
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Kölker, S
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Komini, E
Is the assessment of general movements helpful for the prediction of the neurodevelopmental outcome in a child with symptomatic congenital CMV infection?
Konietzko, A
Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures
König, R
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
König, S
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Korenke, CG
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Korinthenberg, R
Application of Array-based Comparative Genome Hybridization in patients with mental retardation
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Long-term follow up of preterms below 33 weeks of gestation at school age
Korn-Merker, E
Autosomal dominant nocturnal frontal lobe epilepsy in mother and daughter treated with an unusual combination of anticonvulsants
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience
Köstenberger, M
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Kotzaeridou, U
Novel Missence Mutation in the BCS1L Gene as a Cause of mitochondrial encephalopathy with Fanconi Syndrome
Macrocephaly with dilated Virchow-Robin spaces: a new clinical entity?
Koustenis, E
Impairment of executive functions in pediatric posterior fossa tumor survivors
Kraemer, N
The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception
Krägeloh-Mann, I
Evaluation of myotonia and therapeutic implications: about a child with myotonia congenita (Becker disease)
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Editorial
Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis
Kranendijk, M
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Kress, W
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Krieg, EM
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Kruse, B
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Kuhlmann, T
CK elevation and progressive toe walking in a 14-year old girl
Kun, N
Patient safety on a paediatric neurology ward – prevention of drug administration errors by cooperation with clinical pharmacists
Kunz, U
Current practice in the management of newborns with spina bifida in Germany
Kurian, MA
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Kurlemann, G
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
CK elevation and progressive toe walking in a 14-year old girl
Narcolepsy in early childhood – a case study with video
First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood
Kutschke, G
Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse
Kwiecien, R
Postoperative outcome of children with neural tube defects and craniocervical decompression surgery: risk factors with regard to complications and length of hospitalisation
Lackner, H
Infantile Alexander Disease mimicking multilocular astrocytoma
Latal, B
Cerebral MRI findings in adolescents with congenital heart disease
Laufs, M
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Lebrun, AH
Identification of potential biomarkers and modifiers of CLN3-disease progression
Lee-Kirsch, AE
ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome
Leis, T
Preterm and small-for-gestational age: no risk for an adverse cognitive development?
Leiz, S
Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation
Lengnick, K
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Letzgus, A
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
LeVan, P
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Dynamic analysis of absence seizures in humans: all the same but all different
Lewis, T
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Lidzba, K
Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures
Lindbichler, F
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Linder-Lucht, M
Application of Array-based Comparative Genome Hybridization in patients with mental retardation
Lorenz, I
Reflex epilepsy in demyelinating encephalopathy – a case report
Lücke, T
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
BARTH SYNDROME with a new mutation without cardial involvement
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Lütjen, S
Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions
Lütschg, J
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Mader, S
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
Maher, E
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Maier, EM
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Mainberger, F
Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Impaired motor cortex plasticity in patients with Noonan syndrome
Mall, V
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation
Maroske, J
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Marquard, K
Helmets or physiotherapy? Natural history and treatment options for non-synostotic skull deformity in children – results of a literature search
Mattes, D
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
Mattle, HP
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Mauer, UM
Current practice in the management of newborns with spina bifida in Germany
Mautner, VF
Growth hormone treatment of patients with neurofibromatosis type 1
Mayatepek, E
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Optic pathway gliomas in children with neurofibromatosis type 1: a long term study in 38 patients
Mayr, J
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Merkel, HJ
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Meyer, D
Developmental and sex differences of somatosensory perception
Meyer, S
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease
Mildenberger, E
Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Moeller, F
Dynamic analysis of absence seizures in humans: all the same but all different
Moers, A von
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Mohr, A
Polymicrogyria in Fetal Alcohol Syndrome
Möhring, J
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Mole, SE
Identification of potential biomarkers and modifiers of CLN3-disease progression
Möller, F
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Möller-Hartmann, C
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay
Moll-Khosrawi, P
High phenotype variability in CLN3 patients with identical genotype
Morava, E
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Mordekar, S
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Muhle, H
Dynamic analysis of absence seizures in humans: all the same but all different
Mühlhausen, C
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Müller, B
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Müller, HL
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Impaired satiety regulation in obese patients with craniopharyngioma
Müller, K
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls
The concept of modular motor therapy in paediatric neurology
Müller-Schlüter, K
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Müller-Wielsch, K
Developmental retardation due to dietary vitamin B12 deficiency during infancy
Münchau, A
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Munteanu, M
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay
Mürle, B
Macrocephaly with dilated Virchow-Robin spaces: a new clinical entity?
Müther, S
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Muyimbwa, J
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Nagel, A
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results of a longitudinal study
Nagel, C
Growth hormone treatment of patients with neurofibromatosis type 1
Nedeltchev, K
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Neubauer, BA
Singultus as main seizure type in a patient with primary generalized epilepsy
Neuhausen, P
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Niemann, F
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Niggemann, P
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Nögel, SC
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Preterm and small-for-gestational age: no risk for an adverse cognitive development?
Noll, D
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Nolting, HD
From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“
Northam, G
Microstructural alterations of motor pathways in adolescents born preterm
Omran, H
Application of Array-based Comparative Genome Hybridization in patients with mental retardation
Ortfeld, S
Intravenous Lacosamid in refractory convulsive status epilepticus
Ottensmeier, H
A new concept for the neuropsychological testing in very and extreme prematures at the age of more than 5 years
Pape, L
Neurological complications following renal transplantation in infants and children: A retrospective single centre study
Pauen, S
Visual attention performance in term born and preterm infants with different perinatal risk
Pechmann, A
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation
Pelz, S
Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?
Penzien, J
Improvement of SSPE after carbamazepine: natural course or therapeutic effect?
Peraud, A
Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation
Pfurtscheller, K
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Philippi, H
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Pietz, J
Validation of a parent questionnaire on cognitive development in preterm born infants at the (corrected) age of two years
Correlations between early stress experiences and later behavior regulation in premature born toddlers with low and very low birth weight at the age of two years
Visual attention performance in term born and preterm infants with different perinatal risk
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Macrocephaly with dilated Virchow-Robin spaces: a new clinical entity?
Pilhatsch, A
Infantile Alexander Disease mimicking multilocular astrocytoma
Piroth, W
MRI in children with epilepsy and hydrocephalus – the clinical relevance of improved techniques
Pittner, M
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Plecko, B
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
First manifestation and clinical course of eleven paediatric patients with Multiple Sclerosis assigned to the University Hospital of Children and Adolescents of the Medical University Graz from 2001 to 2009
Infantile Alexander Disease mimicking multilocular astrocytoma
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Plecko-Startinig, B
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Plümpe, N
Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?
Pohl, S
Identification of potential biomarkers and modifiers of CLN3-disease progression
Polster, T
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Porto, L
Promising treatment in a boy with creatine transporter deficiency
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Pykal, U
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Qirshi, M
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Bimanual mirror movements in a patient with Kallmann Syndrome
Radkow, T
Reflex epilepsy in demyelinating encephalopathy – a case report
Ramantani, G
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Rapp, EM
Is the assessment of general movements helpful for the prediction of the neurodevelopmental outcome in a child with symptomatic congenital CMV infection?
Rauh, R
Impaired long term potentiation (LTP)-like plasticity in patients with high functiong autism and Asperger syndrome (HFA/AS)
Reihle, C
Helmets or physiotherapy? Natural history and treatment options for non-synostotic skull deformity in children – results of a literature search
Reindl, M
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
Reinhardt, K
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Polymicrogyria in Fetal Alcohol Syndrome
Reitter, B
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Reitter, M
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Reulecke, B
Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation
Reuner, G
Validation of a parent questionnaire on cognitive development in preterm born infants at the (corrected) age of two years
Correlations between early stress experiences and later behavior regulation in premature born toddlers with low and very low birth weight at the age of two years
Visual attention performance in term born and preterm infants with different perinatal risk
Reuner, U
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Reutlinger, C
Intravenous Lacosamid in refractory convulsive status epilepticus
Rhein, M von
Proposal on an evaluation form for the standardized indication of physiotherapy and occupational therapy and scientific application in neonatology
Postoperative outcome of children with neural tube defects and craniocervical decompression surgery: risk factors with regard to complications and length of hospitalisation
Cerebral MRI findings in adolescents with congenital heart disease
Richard, P
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Rodenburg, RJT
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Rödl, S
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Roland-Schäfer, D
Evaluation of myotonia and therapeutic implications: about a child with myotonia congenita (Becker disease)
Romein, E
Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions
Rosenbaum, T
Do hormonal therapies stimulate neurofibroma growth?
Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?
The plexiform neurofibroma is an important differential diagnosis of congenital facial swelling
Optic pathway gliomas in children with neurofibromatosis type 1: a long term study in 38 patients
Roth, C
Impaired satiety regulation in obese patients with craniopharyngioma
Rueckriegel, SM
Impairment of executive functions in pediatric posterior fossa tumor survivors
Ruf, S
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Salomons, G
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Infantile Alexander Disease mimicking multilocular astrocytoma
Sanchez-Albisua, I
Evaluation of myotonia and therapeutic implications: about a child with myotonia congenita (Becker disease)
Sanger, T
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Saraph, V
Urodynamic findings by routine preoperative assessment in 46 scoliotic patients
Sass, JO
Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes
Schallner, J
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Schara, U
ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Scharbert, F
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Scheer, I
Cerebral MRI findings in adolescents with congenital heart disease
Scheffner, T
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis
Schimmel, M
Improvement of SSPE after carbamazepine: natural course or therapeutic effect?
Schlunz-Hendann, M
The plexiform neurofibroma is an important differential diagnosis of congenital facial swelling
Schmidt, J
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Schneider, S
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Schoser, B
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Schrader, C
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Schreiber, G
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Schröder, S
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Impaired satiety regulation in obese patients with craniopharyngioma
Schubert, S
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Schulz, A
High phenotype variability in CLN3 patients with identical genotype
Identification of potential biomarkers and modifiers of CLN3-disease progression
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Schulze-Bonhage, A
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Schwartz, O
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
CK elevation and progressive toe walking in a 14-year old girl
Narcolepsy in early childhood – a case study with video
First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood
Schwarz, M
Postoperative outcome of children with neural tube defects and craniocervical decompression surgery: risk factors with regard to complications and length of hospitalisation
Schwarze, CP
Growth hormone treatment of patients with neurofibromatosis type 1
Schwerin-Nagel, A
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
Schwilling, E
Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures
Schwindt, W
Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
CK elevation and progressive toe walking in a 14-year old girl
Seitz, A
Macrocephaly with dilated Virchow-Robin spaces: a new clinical entity?
Selter, M
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Shamdeen, G
The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease
Shatat, M
The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease
Shazi, N
Steadiness/stability of antiepileptic drugs in serum, plasma and whole-blood samples under various storage methods
Shermin-Levine, S
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Shoukier, M
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
Simbrunner, J
Infantile Alexander Disease mimicking multilocular astrocytoma
Siniatchkin, M
Dynamic analysis of absence seizures in humans: all the same but all different
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Skrabl-Baumgartner, A
Acute blindness – a case report of Neuromyelitis Optica (Devic Syndrome) in adolescence
Smeitink, JAM
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Smitka, M
Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Sommer, A
Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes
Sorantin, E
First manifestation and clinical course of eleven paediatric patients with Multiple Sclerosis assigned to the University Hospital of Children and Adolescents of the Medical University Graz from 2001 to 2009
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Sörensen, N
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Sperner, J
Three Children with Alpers' syndrome 2007–2010
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Spiegler, J
Three Children with Alpers' syndrome 2007–2010
Clinical characterization of Dopa-responsive Dystonia in two brothers with homozygous GCH1 mutations and effects of pre-natal levodopa therapy
Intravenous Lacosamid in refractory convulsive status epilepticus
Spohr, HL
Polymicrogyria in Fetal Alcohol Syndrome
Sprinz, A
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results of a longitudinal study
Stark, W
European paediatric patients with neuromyelitis optica: a good prognosis for most and seronegative to NMO-IgG
Staudt, M
Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions
Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience
Asymmetrical localisation of the motor cortex after perinatally acquired intracerebral hemorrhage: Volume shift versus neuroplasticity
Steinfeld, R
Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism
Steinlin, M
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Stemmler, M
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Stephani, U
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Dynamic analysis of absence seizures in humans: all the same but all different
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Sterl, E
Urodynamic findings by routine preoperative assessment in 46 scoliotic patients
Stettner, GM
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
Stoetter, M
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Storch, S
Identification of potential biomarkers and modifiers of CLN3-disease progression
Storm van's Gravesande, K
Application of Array-based Comparative Genome Hybridization in patients with mental retardation
Stötter, M
Evaluation of myotonia and therapeutic implications: about a child with myotonia congenita (Becker disease)
Strassburg, HM
A new concept for the neuropsychological testing in very and extreme prematures at the age of more than 5 years
Streibert, PF
MRI in children with epilepsy and hydrocephalus – the clinical relevance of improved techniques
Streichert, T
Identification of potential biomarkers and modifiers of CLN3-disease progression
Ströbele, H
A new concept for the neuropsychological testing in very and extreme prematures at the age of more than 5 years
Strobl, K
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Strohbusch, M
Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
Stülpnagel, C von
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Therapy-refractory symptomatic focal epilepsy with methylmalonic aciduria: Case report on positive effect of rufinamide
Tacke, U
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Long-term follow up of preterms below 33 weeks of gestation at school age
Tamaru, A
Postoperative outcome of children with neural tube defects and craniocervical decompression surgery: risk factors with regard to complications and length of hospitalisation
Thiels, C
BARTH SYNDROME with a new mutation without cardial involvement
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Thimm, A
Optic pathway gliomas in children with neurofibromatosis type 1: a long term study in 38 patients
Thomas, K
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Thümmler, K
Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?
Thyen, U
Intravenous Lacosamid in refractory convulsive status epilepticus
Tournier, JD
Microstructural alterations of motor pathways in adolescents born preterm
Trollmann, R
Reflex epilepsy in demyelinating encephalopathy – a case report
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Preterm and small-for-gestational age: no risk for an adverse cognitive development?
Ullrich, K
Identification of potential biomarkers and modifiers of CLN3-disease progression
Ungerath, K
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Urban, C
Infantile Alexander Disease mimicking multilocular astrocytoma
Valsangiacomo, E
Cerebral MRI findings in adolescents with congenital heart disease
van der Knaap, M
Infantile Alexander Disease mimicking multilocular astrocytoma
Vianey-Saban Saban, C
Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency
Vlaho, S
Promising treatment in a boy with creatine transporter deficiency
Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis
Voigt, B
Validation of a parent questionnaire on cognitive development in preterm born infants at the (corrected) age of two years
Correlations between early stress experiences and later behavior regulation in premature born toddlers with low and very low birth weight at the age of two years
Vollmer, B
Microstructural alterations of motor pathways in adolescents born preterm
Vorgerd, M
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
Vry, J
6q13–6q14.1 deletion syndrome characterized by congenital myopathy, mental retardation and minor dysmorphisms – a case report
Wagner, A
Long-term outcome of Alice-in-Wonderland-Syndrome: Results from a case series of 12 patients
Walkenhorst, H
Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases
Walsh, S
Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation
Walter, M
Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes
Weber, K
Asymmetrical localisation of the motor cortex after perinatally acquired intracerebral hemorrhage: Volume shift versus neuroplasticity
Wehrli, E
Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke
Weigt-Usinger, K
BARTH SYNDROME with a new mutation without cardial involvement
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)
Weise, S
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Weiss, D
Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation
Weissert, M
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
Weitkämper, A
BARTH SYNDROME with a new mutation without cardial involvement
Wenzel, D
Reflex epilepsy in demyelinating encephalopathy – a case report
Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Preterm and small-for-gestational age: no risk for an adverse cognitive development?
Weschke, B
Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease
Wessel, V
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Westhoff, B
„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls
Wevers, RA
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Wiegand, C
Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity
Wiegand, G
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Wiesel, T
The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Wilichowski, E
Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene
Wilke, M
Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience
Willichowski, E
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)
Wimmer, K
Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?
Winkler, S
Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures
Wittke, A
Visual attention performance in term born and preterm infants with different perinatal risk
Wochner, K
Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements
Woermann, G
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Wolf, A
L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
Wolff, M
Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis
Wolff, S
EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus
Wortmann, SB
Towards the genetic defect in MEGDEL syndrome: Four novel patients
Wraige, E
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Wyatt, J
Microstructural alterations of motor pathways in adolescents born preterm
Zenker, M
Impaired motor cortex plasticity in patients with Noonan syndrome
Zentner, J
Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time
Zernikow, B
The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception
Zeumer, H
Blindness due to unrecognized bilateral optic nerve sheath meningioma in a 14-year-old girl (case report)
Zielen, S
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Zobel, G
Presentation of 16 paediatric patients manifesting with stroke during 2006–2010
Zschocke, J
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Zsoter, A
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience