Abstracts for the 30th Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)

Adami, A.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Albisetti, M.

Disorders of coagulation – What do they really have to do with pediatric ischemic stroke?

Alroy, J.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Appleton, R. E.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Ausserer, B.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Baldeweg, T.

Novelty event related potential abnormalities in children with infantile spasms

Bani Hashemi, S.

Induction of hypoxia-inducible factor-1α (HIF-1α) and adrenomedullin (ADM) in response to global rat CNS hypoxia

Barth, A.

Unexpected outcome of two patients with acute hemorrhage due to intracranial vascular malformation

Barth, P. G.

X-linked cardioskeletal myopathy and neutropenia

Bast, T.

Source analysis of ictal EEG patterns in focal epilepsy

Bauer, R.

Effects of topiramate after neonatal hypoxia-ischemia

Baumeister, F. A. M.

Quality of life of children with pharmacoresistant epilepsy on ketogenic diet

Carnitine deficiency in children with pharmacoresistant epilepsy during treatment with ketogenic diet

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Efficacy of the ketogenic diet in neurometabolic disorders

Baumgartner, S.

Moya-Moya syndrome and Down syndrome – a case report

First report of a homozygote mutation of MECP2-gene in a female patient with Rett syndrome

EEG-alterations in patients with propionic acidemia

Bax, M.

The European cerebral palsy study: magnetic resonance imaging (MRI) and clinical findings

Bechthold, S.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Benninger, F.

Ictal and interictal nonlinear EEG-dynamics measured with the point prediction error (PPE) in children with temporal lobe epilepsy (TLE)

Left and right hemifield pattern-reversal VEP in primary school children: investigation of components N1, P2 and N2

Berg, J.

Ethosuximide is the drug of choice against epileptic negative myoclonus (ENM)

Berger, C.

Tick-borne encephalitis (TBE) in a 6 week old infant

Bergmann, C.

Hereditary neuropathies in childhood

Bertini, E.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Berweck, S.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Analgosedation in children treated with botulinum-toxin – efficacy and side effects

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Bettendorf, M.

Hypertrophic myopathy, loss of psychomotor skills, and pituitary mass lesion in an infant with hypothyroid auto-immune thyreoiditis

Bevot, A.

The European cerebral palsy study: magnetic resonance imaging (MRI) and clinical findings

Bieniakiewicz, I.

Epilepsy after stroke in childhood

Bigalke, H.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Birnbacher, R.

Cerebellar atrophy in extreme premature infants

Bittigau, P.

Hyperoxia causes brain proteome changes in infant mice

Protective effect of erythropoietin in a neonatal model of brain damage

Blank, R.

Kinematic and kinetic analysis of finger-handmotor function in children with central movement disorders

Bockisch, A.

Dynamic [18F]2-FDG-PET-imaging in patients with GLUT1-deficiency syndrome before and on a ketogenic diet

Boda, V.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Boegl, K.

Clinical experience with substrate reduction therapy in type 1 Gaucher disease

Böhles, H.

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Bollinger, M.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Boltshauser, E.

Outcome of craniopharyngioma in children: long-term complications and quality of life

Familial West syndrome and dystonia caused by ARX gene mutation

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Cerebellar malformations – update

Long-term outcome of 10 patients with opsoclonus-myoclonus syndrome

Born, J.

Learning in sleep: psychological and neurophysiological mechanisms

Boustany, R. M.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Boyd, S.

Novelty event related potential abnormalities in children with infantile spasms

Brandl, U.

Effects of topiramate after neonatal hypoxia-ischemia

Brauss, D. F.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Brodhun, M.

Effects of topiramate after neonatal hypoxia-ischemia

Broxtermann, W.

Congenital myasthenic syndrome in a girl from Albania

Brückner, J.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Brugger, P. C.

Cerebellar atrophy in extreme premature infants

Prenatal diagnosis of rhombencephalosynapsis with fetal MRI

Growth of the human cerebellum

Bruhn, K.

Paroxysmal dystonic choreoathetosis

Brunner-Krainz, M.

Diagnostic findings in acute encephalitis

Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency

Buehrer, C.

Hyperoxia causes brain proteome changes in infant mice

Protective effect of erythropoietin in a neonatal model of brain damage

Burtzlaff, C.

Cognitive evoked potentials in obese children and adolescents

Champion, M. P.

Biotinidase deficiency: a treatable leukoencephalopathy

Chan, A.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

Claes, L.

SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy

Clemens, P. C.

Almost life threatening event in a Prader-Willi syndrome child, at night, after dose increase of growth hormone

Central alveolar hypoventilation (Ondine's curse) in Joubert syndrome

Czech, T.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Das, A.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Das, A. M.

Failure to thrive as clue to diencephalic tumours in infants

Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia

Datta, A. N.

DOPA responsive dystonia and myoclonic epilepsy: case report on an unusual combination of symptoms

Debus, O.

The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study

Hereditary motor and sensory neuropathy (HMSN) Ia with cerebellar hypoplasia and ataxia

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Sulthiame in the initial therapy of West syndrome – update of a prospective placebocontrolled multicenter study

Debus, O. M.

Deficit in P50 sensory gating in children with centrotemporal spikes and sharp waves (CTS) in the EEG. Is there evidence of deficit in family members?

De Jonghe, P.

SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy

Demirakca, T.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Derfler, K.

Successful treatment of dermatomyositis with IgG-apheresis

deVeber, G.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

Dhar, S.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Didiano, D.

Telomere maintenance in childhood primitive neuroectodermal brain tumors

Dieckmann, K.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Ding, X.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Dinger, J.

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Dittrich, S.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Clinical features of cardiomyopathy in muscular dystrophy Duchenne and Becker-Kiener

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Domann, E.

Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Dorn, T.

Epilepsy in children with inv dup(15)

Dötsch, J.

Induction of hypoxia-inducible factor-1α (HIF-1α) and adrenomedullin (ADM) in response to global rat CNS hypoxia

Dralle, D.

Interhemispheric differences of visually evoked potentials (VEP) in children with generalized seizures

Interactions between cortex and brainstem during REM-sleep in preterm and newborn infants with subclinical myoclonus

Dzietko, M.

Protective effect of erythropoietin in a neonatal model of brain damage

Ebach, K.

Mutations in the sodium channel gene SCN1A in myoclonic epilepsies of infancy

Ebinger, F.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Hypertrophic myopathy, loss of psychomotor skills, and pituitary mass lesion in an infant with hypothyroid auto-immune thyreoiditis

Congenital myasthenic syndrome in a girl from Albania

Edlinger-Horvat, C.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Eggermann, T.

Hereditary neuropathies in childhood

Ehehalt, S.

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

Postnatal increase of cerebral perfusion in preterm neonates

Eichholz, S.

Spinal muscular atrophy with respiratory distress tpe 1 (SMARD1) – clinical history and rehabilitation of two 24-hours-home-ventilated children

Emmert, R.

Asymptomatic cortical atrophy of the cerebellum after intoxication with an antiseptic agent

Posterior reversible encephalopathy associated with hypertension in an acute, streptococcal glomerulonephritis

Ensenauer, R.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Erwa, W.

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Everts, R.

Neuropsychological outcome after stroke in childhood

Fahnenstich, H.

Attention-induced bifrontal cerebral hemodynamic changes in boys with attention deficit disorder measured by near-infrared-spectroscopy (NIRS)

Felber, S.

Moya-Moya syndrome and Down syndrome – a case report

EEG-alterations in patients with propionic acidemia

Felderhoff-Mueser, U.

Hyperoxia causes brain proteome changes in infant mice

Protective effect of erythropoietin in a neonatal model of brain damage

Fernandez, E.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Feucht, M.

Ictal and interictal nonlinear EEG-dynamics measured with the point prediction error (PPE) in children with temporal lobe epilepsy (TLE)

Left and right hemifield pattern-reversal VEP in primary school children: investigation of components N1, P2 and N2

Cognitive disabilities of children with a benign partial epilepsy

Mutation screen of the GABAA receptor beta3 subunit gene in patients with childhood absence epilepsy

Vertebral body infarction as a confirmatory sign of anterior spinal artery syndrome – a case report

Successful treatment of dermatomyositis with IgG-apheresis

Fiedler, B.

Deficit in P50 sensory gating in children with centrotemporal spikes and sharp waves (CTS) in the EEG. Is there evidence of deficit in family members?

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Fietzek, U.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Fietzek, U. M.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Analgosedation in children treated with botulinum-toxin – efficacy and side effects

Fischer, Doris

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Fliegauf, M.

NPHP3 expression in ciliated neural precursor cells of the cerebellum suggests a specific function of nephrocystin-3 for cerebellar development

Flodmark, O.

The European cerebral palsy study: magnetic resonance imaging (MRI) and clinical findings

Fowler, B.

GM1 gangliosidosis – therapeutical trial with Miglustat (Zavesca®) – a case report

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Francke, A.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Freilinger, M.

Vertebral body infarction as a confirmatory sign of anterior spinal artery syndrome – a case report

Freisinger, P.

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Efficacy of the ketogenic diet in neurometabolic disorders

Friebel, D.

Transient ischemic attack (TIA) in a child with severe transient erythroblastopenia of childhood (TEC) – causal relation or coincidence?

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Frohnhöfer, M.

Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated?

Frölich, J.

Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia

Fuchs, K.

Mutation screen of the GABAA receptor beta3 subunit gene in patients with childhood absence epilepsy

Fuhrer, K.

Unexpected outcome of two patients with acute hemorrhage due to intracranial vascular malformation

Fusch, C.

Cognitive evoked potentials in obese children and adolescents

Gaa, J.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Gadner, H.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Ganesan, V.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

Gärtner, J.

Rett syndrome without mutations in the MECP2-Gene

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome

Gasparini, M.

A novel mutation (86insA) in the alpha-sarcoglycan-gene leads to severe childhood autosomal recessive muscular dystrophy

Gebhardt, B.

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Gelpi, E.

Successful treatment of dermatomyositis with IgG-apheresis

Gempel, K.

Carnitine deficiency in children with pharmacoresistant epilepsy during treatment with ketogenic diet

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Efficacy of the ketogenic diet in neurometabolic disorders

Gerloff, C.

Mirror movements in congenital hemiparesis: a clinical indicator for ipsilateral cortico-spinal projections from the intact hemisphere?

Gerstl, J.

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Analgosedation in children treated with botulinum-toxin – efficacy and side effects

Gerstner, T.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Geth, K.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Goelz, R.

Postnatal increase of cerebral perfusion in preterm neonates

Gooding, R.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Göppel, C.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Gortner, L.

Interactions between cortex and brainstem during REM-sleep in preterm and newborn infants with subclinical myoclonus

Gottwald, T.

Moya-Moya syndrome and Down syndrome – a case report

Grill, I.

Interactions between cortex and brainstem during REM-sleep in preterm and newborn infants with subclinical myoclonus

Grodd, W.

Routine MRI visibility of ipsilateral cortico-spinal pathways in congenital hemiparesis

Grohmann, K.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Grolik, A.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Gross, C.

Familial West syndrome and dystonia caused by ARX gene mutation

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

Groß, S.

Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Grotzer, M. A.

Outcome of craniopharyngioma in children: long-term complications and quality of life

Telomere maintenance in childhood primitive neuroectodermal brain tumors

Gruber-Sedlmayr, U.

Diagnostic findings in acute encephalitis

SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy

Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency

Grünewald, S.

O-glycosylation defects with structural changes of the central nervous system – new members of the CDG family

Biotinidase deficiency: a treatable leukoencephalopathy

Guenther, U. P.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Gutmann, I.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Haberlandt, E.

Moya-Moya syndrome and Down syndrome – a case report

First report of a homozygote mutation of MECP2-gene in a female patient with Rett syndrome

EEG-alterations in patients with propionic acidemia

Haberler, C.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Haffkemeyer, U.

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Hagel, C.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Hahn, A.

Beta-2-glykoprotein 1 antibodies in an infant with recurrent strokes and familial predisposition for systemic lupus erythematosus

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Hahn, H.

Unilateral pes cavus caused by a thoracic intradural arachnoid cyst

Hainfellner, J.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Hamm, A.

Cognitive evoked potentials in obese children and adolescents

Handwerker, G.

Sleep-disordered breathing in myelomeningocele

Hanefeld, F.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Hansen, H. H.

Protective effect of erythropoietin in a neonatal model of brain damage

Harjes, M.

Miller-Fisher syndrome: when the eyes don’t move and the body can’t stand still

Harting, I.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Hartmann, H.

Failure to thrive as clue to diencephalic tumours in infants

Hasselmann, O.

Reversible posterior leucoencephalopathy (RPLS) in childhood – seldom reported, poorly understood

Häusler, M.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Diagnosis of neurological complications related to reactivated EBV infection

Heckel, M.

Mitoxantrone therapy in two patients with deteriorating remitting-relapsing multiple sclerosis

Hehr, U.

Familial West syndrome and dystonia caused by ARX gene mutation

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

Heimkes, B.

Unilateral pes cavus caused by a thoracic intradural arachnoid cyst

Heinen, F.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Efficacy of BTX/A in the treatment of adductor spasticity: a randomized, double blinded, placebo-controlled trial

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Henneke, M.

Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome

Hennies, H. C.

Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome

Herkenrath, P.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Herpers, M.

Age-related activation of the cingulate motor area

Herrmann, J.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Herweh, C.

Hypertrophic myopathy, loss of psychomotor skills, and pituitary mass lesion in an infant with hypothyroid auto-immune thyreoiditis

Heubner, G. L.

Transient ischemic attack (TIA) in a child with severe transient erythroblastopenia of childhood (TEC) – causal relation or coincidence?

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Hof, D.

Moya-Moya syndrome and Down syndrome – a case report

Hofbeck, M.

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

Hoffmann, G. F.

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Hoffmann, K.

Ictal and interictal nonlinear EEG-dynamics measured with the point prediction error (PPE) in children with temporal lobe epilepsy (TLE)

Left and right hemifield pattern-reversal VEP in primary school children: investigation of components N1, P2 and N2

Holthausen, H.

Ethosuximide is the drug of choice against epileptic negative myoclonus (ENM)

Epilepsy after stroke in childhood

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Longterm retention rates of the newer antiepileptic drugs (FBM, GBP, LEV, LTG, OXC, TPM, TGB, VGB) in childhood epilepsies difficult to treat

Hübner, C.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Huemer, C.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Hügens-Penzel, M.

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

Huppke, P.

Rett syndrome without mutations in the MECP2-Gene

Hußmann, O.

Beta-2-glykoprotein 1 antibodies in an infant with recurrent strokes and familial predisposition for systemic lupus erythematosus

Hytopoulos, A.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Iff, T.

Tick-borne encephalitis (TBE) in a 6 week old infant

Ikonomidou, C.

Hyperoxia causes brain proteome changes in infant mice

Protective effect of erythropoietin in a neonatal model of brain damage

Ipsiroglu, O. S.

Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients

Item, C.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Ittner, K.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Jansen, M.

Successful treatment of dermatomyositis with IgG-apheresis

Janssen, A.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Jansson, A.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Jenni, O. G.

Sleep disorders during childhood

Joncourt, F.

A novel mutation (86insA) in the alpha-sarcoglycan-gene leads to severe childhood autosomal recessive muscular dystrophy

Jost, W.

Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated?

Jourdan, S.

Periodic breathing in neonates. A proposal for differentiation in central and obstructive patterns

Alice in Wonderland syndrome: clinical features and differential diagnosis

Jourdan Moser, S.

EEG characteristics in Rett syndrome

Fast improvement of verbal memory function after left temporal tumor resection

Kafadar, I.

Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Kaindl, A. M.

Hyperoxia causes brain proteome changes in infant mice

Kalaydjieva, L.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Kaltenbrunner, K.

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Kammerer, G.

Source analysis of ictal EEG patterns in focal epilepsy

Kannt, O.

Almost life threatening event in a Prader-Willi syndrome child, at night, after dose increase of growth hormone

Central alveolar hypoventilation (Ondine's curse) in Joubert syndrome

Kanzelmeyer, N.

Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia

Kaufmann, F.

Neuropsychological outcome after stroke in childhood

Kececioglu, D.

Clinical features of cardiomyopathy in muscular dystrophy Duchenne and Becker-Kiener

Kehrer, M.

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

Postnatal increase of cerebral perfusion in preterm neonates

Keimer, R.

Hereditary neuropathy with liability to pressure palsies (HNPP) with progressive deafness and demyelination in the central nervous system

Kienle, M.

Deficit in P50 sensory gating in children with centrotemporal spikes and sharp waves (CTS) in the EEG. Is there evidence of deficit in family members?

Kieslich, M.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Kirchmann, C.

Clinical features of cardiomyopathy in muscular dystrophy Duchenne and Becker-Kiener

Kirkham, F.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

Kirschner, J. B.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Kispert, A.

NPHP3 expression in ciliated neural precursor cells of the cerebellum suggests a specific function of nephrocystin-3 for cerebellar development

Klein, A.

Long-term outcome of 10 patients with opsoclonus-myoclonus syndrome

Klein, W.

Unexpected clinical course in a 9-year-old boy with congenital hypomyelinating neuropathy due to a novel MPZ gene mutation

Kleines, M.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Diagnosis of neurological complications related to reactivated EBV infection

Klepper, J.

Dynamic [18F]2-FDG-PET-imaging in patients with GLUT1-deficiency syndrome before and on a ketogenic diet

Klose, J.

Hyperoxia causes brain proteome changes in infant mice

Kluger, G.

Ethosuximide is the drug of choice against epileptic negative myoclonus (ENM)

Epilepsy after stroke in childhood

St Valentine – patron saint of epilepsy – illustrating the semiology of childhood seizures over ther course of six centuries

Longterm retention rates of the newer antiepileptic drugs (FBM, GBP, LEV, LTG, OXC, TPM, TGB, VGB) in childhood epilepsies difficult to treat

Koch, H. G.

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Koch, M. J.

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Kohlschütter, A.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Kolditz, P.

Reversible posterior leucoencephalopathy (RPLS) in childhood – seldom reported, poorly understood

König, S.

Influence of valproate, carbamazepine and antiepileptic polytherapy on free carnitine in pediatric patients

König, S. A.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Konstantopoulou, V.

EEG-alterations in patients with propionic acidemia

Kontopoulos, E.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Korall, H.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Korinthenberg, R.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Efficacy of BTX/A in the treatment of adductor spasticity: a randomized, double blinded, placebo-controlled trial

Neuronal plasticity II: modulation of cortical excitability

Neuronal plasticity I – maturation of cortical excitability

Inflammatory neuropathies in childhood – update

Clinical features of cardiomyopathy in muscular dystrophy Duchenne and Becker-Kiener

Age-related activation of the cingulate motor area

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Kosch, A.

The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study

Krägeloh-Mann, I.

The European cerebral palsy study: magnetic resonance imaging (MRI) and clinical findings

Mirror movements in congenital hemiparesis: a clinical indicator for ipsilateral cortico-spinal projections from the intact hemisphere?

Routine MRI visibility of ipsilateral cortico-spinal pathways in congenital hemiparesis

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

The reference and training manual of the SCPE (surceillance of cerebral palsy in europe)

Krämer, N.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Krammer, U.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Krauß, J.

Sleep-disordered breathing in myelomeningocele

Kretzschmar, B.

Spinal muscular atrophy with respiratory distress tpe 1 (SMARD1) – clinical history and rehabilitation of two 24-hours-home-ventilated children

Kudernatsch, V.

St Valentine – patron saint of epilepsy – illustrating the semiology of childhood seizures over ther course of six centuries

Kuhlenbaeumer, G.

Hereditary motor and sensory neuropathy (HMSN) Ia with cerebellar hypoplasia and ataxia

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Küker, W.

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

Kurlemann, G.

Deficit in P50 sensory gating in children with centrotemporal spikes and sharp waves (CTS) in the EEG. Is there evidence of deficit in family members?

Hereditary motor and sensory neuropathy (HMSN) Ia with cerebellar hypoplasia and ataxia

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Sulthiame in the initial therapy of West syndrome – update of a prospective placebocontrolled multicenter study

Kurnik, K.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Laccone, F.

Rett syndrome without mutations in the MECP2-Gene

Lang, D.

Telomere maintenance in childhood primitive neuroectodermal brain tumors

Lange, P.

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Langen, H.

Failure to thrive as clue to diencephalic tumours in infants

Lauffer, H.

Cognitive evoked potentials in obese children and adolescents

Lechner-Pissenberger, S.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Leiz, S.

Unilateral pes cavus caused by a thoracic intradural arachnoid cyst

Leonard, J. V.

Biotinidase deficiency: a treatable leukoencephalopathy

Liebhaber, G.

Quality of life of children with pharmacoresistant epilepsy on ketogenic diet

Carnitine deficiency in children with pharmacoresistant epilepsy during treatment with ketogenic diet

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Efficacy of the ketogenic diet in neurometabolic disorders

Lin, S.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Linder, M.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Neuronal plasticity II: modulation of cortical excitability

Age-related activation of the cingulate motor area

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Lindmayer, F.

Implantation of an intrathecal pump for baclofen administration in an outpatient setting

Lochmüller, H.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Löscher, W.

Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency

Lücke, T.

Failure to thrive as clue to diencephalic tumours in infants

Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia

Lütjen, S.

Epilepsy after stroke in childhood

Lütschg, J.

EEG characteristics in Rett syndrome

DOPA responsive dystonia and myoclonic epilepsy: case report on an unusual combination of symptoms

Periodic breathing in neonates. A proposal for differentiation in central and obstructive patterns

Alice in Wonderland syndrome: clinical features and differential diagnosis

Fast improvement of verbal memory function after left temporal tumor resection

Attention-induced bifrontal cerebral hemodynamic changes in boys with attention deficit disorder measured by near-infrared-spectroscopy (NIRS)

Hereditary neuropathies – a clinical overview

GM1 gangliosidosis – therapeutical trial with Miglustat (Zavesca®) – a case report

Maier, Ute

Transient ischemic attack (TIA) in a child with severe transient erythroblastopenia of childhood (TEC) – causal relation or coincidence?

Mall, V.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Efficacy of BTX/A in the treatment of adductor spasticity: a randomized, double blinded, placebo-controlled trial

Neuronal plasticity II: modulation of cortical excitability

Neuronal plasticity I – maturation of cortical excitability

Age-related activation of the cingulate motor area

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Marquard, K.

Hereditary neuropathy with liability to pressure palsies (HNPP) with progressive deafness and demyelination in the central nervous system

Martin, G.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Mayatepek, E.

Miller-Fisher syndrome: when the eyes don’t move and the body can’t stand still

Mitoxantrone therapy in two patients with deteriorating remitting-relapsing multiple sclerosis

Mayer, B.

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Mayer, T. E.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Meier, R.

Tick-borne encephalitis (TBE) in a 6 week old infant

Mercimek-Mahmutoglu, S.

Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Merkenschlager, A.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Messerschmidt, A.

Cerebellar atrophy in extreme premature infants

Michaelis, U.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Minet, J. C.

Periodic breathing in neonates. A proposal for differentiation in central and obstructive patterns

GM1 gangliosidosis – therapeutical trial with Miglustat (Zavesca®) – a case report

Mittermayer, C.

Prenatal diagnosis of rhombencephalosynapsis with fetal MRI

Moers, A. von

Identification of transcripts from a subtraction library in an intrafamilially variable course of Duchenne muscular dystrophy

Möller, U.

Ictal and interictal nonlinear EEG-dynamics measured with the point prediction error (PPE) in children with temporal lobe epilepsy (TLE)

Monros, E.

First report of a homozygote mutation of MECP2-gene in a female patient with Rett syndrome

Morris, A. A. M.

Biotinidase deficiency: a treatable leukoencephalopathy

Mortier, W.

Unexpected clinical course in a 9-year-old boy with congenital hypomyelinating neuropathy due to a novel MPZ gene mutation

Moser, E.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Mücher, J.

Hypertrophic myopathy, loss of psychomotor skills, and pituitary mass lesion in an infant with hypothyroid auto-immune thyreoiditis

Müller, S. P.

Dynamic [18F]2-FDG-PET-imaging in patients with GLUT1-deficiency syndrome before and on a ketogenic diet

Müller, T.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Müller-Stöver, S.

Sleep-disordered breathing in myelomeningocele

Müllner-Eidenböck, A.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Nagel, S.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Neophytou, B.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Neubauer, B.

Beta-2-glykoprotein 1 antibodies in an infant with recurrent strokes and familial predisposition for systemic lupus erythematosus

Mutations in the sodium channel gene SCN1A in myoclonic epilepsies of infancy

Neubauer, B. A.

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

Fluctuating ataxia in a child with short-intestine-syndrome and D-lactate acidosis

Neuberger, J.

Asymptomatic cortical atrophy of the cerebellum after intoxication with an antiseptic agent

Posterior reversible encephalopathy associated with hypertension in an acute, streptococcal glomerulonephritis

Neuen-Jacob, E.

Congenital peripheral neuropathy with optic atrophy and symmetric white matter lesions

Neumaier Probst, E.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Neville, B.

Novelty event related potential abnormalities in children with infantile spasms

Nowak-Göttl, U.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study

Oberhoffer, R.

Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy

Olah, E.

Tick-borne encephalitis (TBE) in a 6 week old infant

Olbrich, H.

NPHP3 expression in ciliated neural precursor cells of the cerebellum suggests a specific function of nephrocystin-3 for cerebellar development

Omran, H.

NPHP3 expression in ciliated neural precursor cells of the cerebellum suggests a specific function of nephrocystin-3 for cerebellar development

Opladen, T.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Otto, M.

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Parbel, S.

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Patt, S.

Effects of topiramate after neonatal hypoxia-ischemia

Pavlou, E.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Pavlovic, J.

Paediatric stroke – differences to adult stroke

Petruch, U.

The reference and training manual of the SCPE (surceillance of cerebral palsy in europe)

Peyrl, A.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Peyro-Saint-Paul, H.

Clinical experience with substrate reduction therapy in type 1 Gaucher disease

Pfluger, T.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Pieper, T.

Epilepsy after stroke in childhood

Plecko, B.

Diagnostic findings in acute encephalitis

SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy

Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Poets, C.

Postnatal increase of cerebral perfusion in preterm neonates

Pohl, D.

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Polster, T.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Poretti, A.

Outcome of craniopharyngioma in children: long-term complications and quality of life

Portisch, A.

Interhemispheric differences of visually evoked potentials (VEP) in children with generalized seizures

Porto, L.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Pöschl, J.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Pranzatelli, M. R.

Opsoclonus-myoclonus syndrome: diagnostic and therapeutic considerations

Prayer, D.

Cerebellar atrophy in extreme premature infants

Vertebral body infarction as a confirmatory sign of anterior spinal artery syndrome – a case report

Prenatal diagnosis of rhombencephalosynapsis with fetal MRI

Growth of the human cerebellum

Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients

Preuß, N.

Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome

Raikhman, P.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Ramaekers, V. T.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Diagnosis of neurological complications related to reactivated EBV infection

Ramantani, G.

Source analysis of ictal EEG patterns in focal epilepsy

Ramelli, G. P.

A novel mutation (86insA) in the alpha-sarcoglycan-gene leads to severe childhood autosomal recessive muscular dystrophy

Rascher, W.

Induction of hypoxia-inducible factor-1α (HIF-1α) and adrenomedullin (ADM) in response to global rat CNS hypoxia

Rating, D.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Laboratory controls and therapeutic antiepileptic drug monitoring during the treatment of children with epilepsy – sense or nonsense – PRO

Source analysis of ictal EEG patterns in focal epilepsy

Hypertrophic myopathy, loss of psychomotor skills, and pituitary mass lesion in an infant with hypothyroid auto-immune thyreoiditis

Congenital myasthenic syndrome in a girl from Albania

Redbrake, A.

Ethosuximide is the drug of choice against epileptic negative myoclonus (ENM)

Reichenbach, J.

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Reiter, D.

Left and right hemifield pattern-reversal VEP in primary school children: investigation of components N1, P2 and N2

Reiter, E.

Vertebral body infarction as a confirmatory sign of anterior spinal artery syndrome – a case report

Ribi, K.

Outcome of craniopharyngioma in children: long-term complications and quality of life

Riemann, E.

Efficacy of the ketogenic diet in neurometabolic disorders

Ries, M.

Asymptomatic cortical atrophy of the cerebellum after intoxication with an antiseptic agent

Posterior reversible encephalopathy associated with hypertension in an acute, streptococcal glomerulonephritis

Rinnert, S.

Paroxysmal dystonic choreoathetosis

Ritter, K.

Diagnosis of neurological complications related to reactivated EBV infection

Riva, D.

Cerebellum and cognition

Rohrer, T.

Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated?

Rona, S.

Source analysis of ictal EEG patterns in focal epilepsy

Roschitz, B.

SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy

Rose, C.

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Rosenbaum, T.

Miller-Fisher syndrome: when the eyes don’t move and the body can’t stand still

Mitoxantrone therapy in two patients with deteriorating remitting-relapsing multiple sclerosis

Rosenow, D.

Implantation of an intrathecal pump for baclofen administration in an outpatient setting

Rossi, R.

The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study

Rostasy, K.

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Rübo, J.

Miller-Fisher syndrome: when the eyes don’t move and the body can’t stand still

Rudnik-Schöneborn, S.

Hereditary neuropathies in childhood

Rylova, S.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Sagi, D.

Hyperoxia causes brain proteome changes in infant mice

Sälke-Kellermann, R.

Epilepsy in children with inv dup(15)

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Sandkoetter, J.

Deficit in P50 sensory gating in children with centrotemporal spikes and sharp waves (CTS) in the EEG. Is there evidence of deficit in family members?

Hereditary motor and sensory neuropathy (HMSN) Ia with cerebellar hypoplasia and ataxia

Schäfer, H.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Schallner, J. C.

Transient ischemic attack (TIA) in a child with severe transient erythroblastopenia of childhood (TEC) – causal relation or coincidence?

Schaper, J.

Biotinidase deficiency: a treatable leukoencephalopathy

Schara, U.

Unexpected clinical course in a 9-year-old boy with congenital hypomyelinating neuropathy due to a novel MPZ gene mutation

Scheithauer, S.

Diagnosis of neurological complications related to reactivated EBV infection

Schelle, A.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Age-related activation of the cingulate motor area

Schenk, B.

Almost life threatening event in a Prader-Willi syndrome child, at night, after dose increase of growth hormone

Central alveolar hypoventilation (Ondine's curse) in Joubert syndrome

Scherg, M.

Source analysis of ictal EEG patterns in focal epilepsy

Schessl, J.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Neuronal plasticity II: modulation of cortical excitability

Neuronal plasticity I – maturation of cortical excitability

Clinical features of cardiomyopathy in muscular dystrophy Duchenne and Becker-Kiener

Schmid, H. J.

Failure to thrive as clue to diencephalic tumours in infants

Schmitt, B.

Familial West syndrome and dystonia caused by ARX gene mutation

Startle induced epileptic seizures: a clinical and electrophysiological review of 22 children

Sleep and epilepsy

Long-term outcome of 10 patients with opsoclonus-myoclonus syndrome

Schmitt-Mechelke, T.

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Schneider, A.

Posterior reversible encephalopathy associated with hypertension in an acute, streptococcal glomerulonephritis

Schneider, J. F. L.

Tick-borne encephalitis (TBE) in a 6 week old infant

Schneider, W.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Scholl-Bürgi, S.

EEG-alterations in patients with propionic acidemia

Schöning, M.

Prenatal multicystic encephalomalacia caused by an anomaly of the aortic arch

Postnatal increase of cerebral perfusion in preterm neonates

Schönle, E.

Outcome of craniopharyngioma in children: long-term complications and quality of life

Schrader, K.

Congenital myasthenic syndrome in a girl from Albania

Schreiner, A.

Efficacy and tolerability of topiramate in children and adolescents with partial or primary generalized epilepsy

Monotherapy in newly diagnosed epilepsy: findings in the pediatric subset of a comparative study of topiramate, carbamazepine, and valproate

Schröder, C.

Cognitive evoked potentials in obese children and adolescents

Schröder, J. M.

Unexpected clinical course in a 9-year-old boy with congenital hypomyelinating neuropathy due to a novel MPZ gene mutation

Schroeder, A. S.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Analgosedation in children treated with botulinum-toxin – efficacy and side effects

Schropp, C.

Sleep-disordered breathing in myelomeningocele

Schroth, G.

Unexpected outcome of two patients with acute hemorrhage due to intracranial vascular malformation

Schubert, R.

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Schubert, S.

Effects of topiramate after neonatal hypoxia-ischemia

Schuelke, M.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Schulte Mönting, J.

High prevalence of antibody formation against botulinumtoxin A in the treatment of children – a long-term cohort study in the years 1993–2001

Schulz, A.

Impaired cell adhesion and apoptosis in the novel CLN9 Batten disease variant

Schulze, A.

Influence of valproate, carbamazepine and antiepileptic polytherapy on free carnitine in pediatric patients

Schumacher, M.

Age-related activation of the cingulate motor area

Schweizer, K.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Schwerin, A.

Retrospective analysis comparing proximal injection of the iliopsoas muscle versus sonography-guided distal injection (SIMPLE)

Multilevel treatment – safety of the 12Plus-concept with botulinum toxin A (Botox®)

Analgosedation in children treated with botulinum-toxin – efficacy and side effects

Scott, R. C.

Novelty event related potential abnormalities in children with infantile spasms

Seidl, R.

Vertebral body infarction as a confirmatory sign of anterior spinal artery syndrome – a case report

Seitz, A.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Sellhaus, B.

Flow cytometrical analysis of cerebrospinal fluid leukocytes in pediatric patients

Senderek, J.

Hereditary neuropathies in childhood

Shalaby, T.

Telomere maintenance in childhood primitive neuroectodermal brain tumors

Shamdeen, M. G.

Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated?

Sieb, J.

Congenital myasthenic syndrome in a girl from Albania

Sieb, J. P.

Congenital myasthenia with homozygotic mutation N88K of the rapsyn gene with infect associated respiratory insufficiency

Siebel, A.

Efficacy of BTX/A in the treatment of adductor spasticity: a randomized, double blinded, placebo-controlled trial

Sieghart, W.

Mutation screen of the GABAA receptor beta3 subunit gene in patients with childhood absence epilepsy

Sifringer, M.

Hyperoxia causes brain proteome changes in infant mice

Identification of transcripts from a subtraction library in an intrafamilially variable course of Duchenne muscular dystrophy

Protective effect of erythropoietin in a neonatal model of brain damage

Simbrunner, J.

Diagnostic findings in acute encephalitis

Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration

Simma, B.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Skladal, D.

Moya-Moya syndrome and Down syndrome – a case report

First report of a homozygote mutation of MECP2-gene in a female patient with Rett syndrome

EEG-alterations in patients with propionic acidemia

Slavc, I.

Medulloblastoma: the Vienna experience in improvement of overall survival rates between 1969 and 2000

Smeitink, J.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Speer, A.

Identification of transcripts from a subtraction library in an intrafamilially variable course of Duchenne muscular dystrophy

Spreer, J.

Age-related activation of the cingulate motor area

Springer, S.

Stroke due to isolated angiitis ot the central nervous system (CNS) – differential diagnosis and therapy

Staudt, M.

Mirror movements in congenital hemiparesis: a clinical indicator for ipsilateral cortico-spinal projections from the intact hemisphere?

Routine MRI visibility of ipsilateral cortico-spinal pathways in congenital hemiparesis

Steinborn, M.

Unilateral pes cavus caused by a thoracic intradural arachnoid cyst

Steinlein, O.

Congenital myasthenic syndrome in a girl from Albania

Steinlin, M.

Unexpected outcome of two patients with acute hemorrhage due to intracranial vascular malformation

Paediatric stroke – differences to adult stroke

Stephani, U.

Paroxysmal dystonic choreoathetosis

Mutations in the sodium channel gene SCN1A in myoclonic epilepsies of infancy

Laboratory controls and therapeutic antiepileptic drug monitoring during the treatment of children with epilepsy – sense or nonsense – Contra

Stöckler-Ipsiroglu, S.

Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Straßburg, H. M.

Sleep-disordered breathing in myelomeningocele

Sträter, R.

Recurrent arterial ischemic stroke in childhood: the role of prothrombotic disorders and underlying conditions

The factor V G1691A mutation is significantly associated with childhood porencephaly in white children – a case-control-study

Straub, V.

O-glycosylation defects with structural changes of the central nervous system – new members of the CDG family

Streif, W.

Moya-Moya syndrome and Down syndrome – a case report

Stromberger, C.

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Sungurtekin, I.

Functional-MRI for school-aged children with neonatal phenobarbitone medication

Tegtmeyer, F. K.

Spinal muscular atrophy with respiratory distress tpe 1 (SMARD1) – clinical history and rehabilitation of two 24-hours-home-ventilated children

Tibussek, D.

Startle induced epileptic seizures: a clinical and electrophysiological review of 22 children

Tick-borne encephalitis (TBE) in a 6 week old infant

Töller, J.

Interhemispheric differences of visually evoked potentials (VEP) in children with generalized seizures

Interactions between cortex and brainstem during REM-sleep in preterm and newborn infants with subclinical myoclonus

Tonin, P.

A novel mutation (86insA) in the alpha-sarcoglycan-gene leads to severe childhood autosomal recessive muscular dystrophy

Tonn, J. C.

Unilateral pes cavus caused by a thoracic intradural arachnoid cyst

Trijbels, F.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Trinka, E.

EEG-alterations in patients with propionic acidemia

Trollmann, R.

Induction of hypoxia-inducible factor-1α (HIF-1α) and adrenomedullin (ADM) in response to global rat CNS hypoxia

Tryfonas, D.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Tscharre, A.

Prothrombotic risk factors and vasculopathies in children after stroke – consequences for treatment

Tsikoulas, I.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Tydeman, C.

The European cerebral palsy study: magnetic resonance imaging (MRI) and clinical findings

Tzikas, D.

Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia

Uhlenberg, B.

Identification of transcripts from a subtraction library in an intrafamilially variable course of Duchenne muscular dystrophy

Ullrich, K.

Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver

Urak, L.

Mutation screen of the GABAA receptor beta3 subunit gene in patients with childhood absence epilepsy

Successful treatment of dermatomyositis with IgG-apheresis

Utzig, N.

Cognitive evoked potentials in obese children and adolescents

Uyanik, G.

Familial West syndrome and dystonia caused by ARX gene mutation

X-linked lissencephaly with abnormal genitalia (XLAG) associated with renal phosphate wasting and exocrine pancreatic insufficiency

van der Knaap, M.

Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients

Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency

Vargiami, E.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Varon, R.

A heterozygous genomic rearrangement in a patient with juvenile spinal muscle atrophy with respiratory distress type 1 (SMARD1)

Veldman, A.

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Vlaho, S.

Moya-Moya-syndrome: massive lepto-meningeal enhancement in cMRI mimicking impairment of blood-brain barrier

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission

Imbalance of biogenic amines in patients with compulsive disorders and tics

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Voit, T.

O-glycosylation defects with structural changes of the central nervous system – new members of the CDG family

Dynamic [18F]2-FDG-PET-imaging in patients with GLUT1-deficiency syndrome before and on a ketogenic diet

Völkl-Kernstock, S.

Cognitive disabilities of children with a benign partial epilepsy

von Voss, H.

Kinematic and kinetic analysis of finger-handmotor function in children with central movement disorders

Walter, M.

Neurological features of the CCFDN (congenital cataracts facial dysmorphism neuropathy)-syndrome

Walther, M.

Off-label-use of botulinum toxin a (BTX A) in pediatric patients

Neuronal plasticity II: modulation of cortical excitability

Neuronal plasticity I – maturation of cortical excitability

Wang, S.

Monotherapy in newly diagnosed epilepsy: findings in the pediatric subset of a comparative study of topiramate, carbamazepine, and valproate

Weber, L.

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Weber, P.

DOPA responsive dystonia and myoclonic epilepsy: case report on an unusual combination of symptoms

Alice in Wonderland syndrome: clinical features and differential diagnosis

Fast improvement of verbal memory function after left temporal tumor resection

Attention-induced bifrontal cerebral hemodynamic changes in boys with attention deficit disorder measured by near-infrared-spectroscopy (NIRS)

Weber, P. M.

The reference and training manual of the SCPE (surceillance of cerebral palsy in europe)

Weber, R.

Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated?

Wehner, L. E.

Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome

Weibel, L.

Tick-borne encephalitis (TBE) in a 6 week old infant

Weidauer, S.

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Weissert, M.

Epilepsy in children with inv dup(15)

Reversible posterior leucoencephalopathy (RPLS) in childhood – seldom reported, poorly understood

Welte, K.

Failure to thrive as clue to diencephalic tumours in infants

Wenzel, D.

Induction of hypoxia-inducible factor-1α (HIF-1α) and adrenomedullin (ADM) in response to global rat CNS hypoxia

Wenzel, S.

Sleep-disordered breathing in myelomeningocele

Werner, K.

Novelty event related potential abnormalities in children with infantile spasms

Werner, T.

Influence of valproate, carbamazepine and antiepileptic polytherapy on free carnitine in pediatric patients

Wevers, R.

O-glycosylation defects with structural changes of the central nervous system – new members of the CDG family

Wheless, J.

Monotherapy in newly diagnosed epilepsy: findings in the pediatric subset of a comparative study of topiramate, carbamazepine, and valproate

Will, Heike

Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation

Willinger, U.

Cognitive disabilities of children with a benign partial epilepsy

Withut, E.

Tau, phospho-tau and S-100B protein in cerebrospinal fluid of children with multiple sclerosis

Witte, H.

Ictal and interictal nonlinear EEG-dynamics measured with the point prediction error (PPE) in children with temporal lobe epilepsy (TLE)

Left and right hemifield pattern-reversal VEP in primary school children: investigation of components N1, P2 and N2

Witzleb, W.

Mycoplasma pneumoniae-encephalitis in childhood with cardiac impact

Wohlrab, G.

Familial West syndrome and dystonia caused by ARX gene mutation

Startle induced epileptic seizures: a clinical and electrophysiological review of 22 children

Wolf, N. I.

Cortical and subcortical haemorrhagic necrosis as neonatal manifestation of incontinentia pigmenti

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Wörle, H.

Hereditary neuropathy with liability to pressure palsies (HNPP) with progressive deafness and demyelination in the central nervous system

Young, P.

Hereditary motor and sensory neuropathy (HMSN) Ia with cerebellar hypoplasia and ataxia

Early lethal Dejerine-Sottas syndrome in a 13-year-old girl with a point mutation in the MPZ-gene also found in the asymptomatic father

Zafeiriou, D. I.

Botulinum toxin type A treatment in children with spastic cerebral palsy: documentation of the short-term effect with general motor function-measure (GMFM)

Zaik, M.

O-glycosylation defects with structural changes of the central nervous system – new members of the CDG family

Zenz, W.

Diagnostic findings in acute encephalitis

Zerres, K.

Hereditary neuropathies in childhood

Zielen, S.

Cranial magnetic resonance imaging findings in ataxia telangiectasia

Zimmerhackl, L. B.

EEG-alterations in patients with propionic acidemia

Zoder, G.

Cerebellar atrophy in extreme premature infants

Zschocke, J.

Leukoencephalopathy with ataxia, hypodontia and elevation of myo-inositol: a new entity?

Zsótér, A.

Longterm retention rates of the newer antiepileptic drugs (FBM, GBP, LEV, LTG, OXC, TPM, TGB, VGB) in childhood epilepsies difficult to treat

Özkan, Ö

Source analysis of ictal EEG patterns in focal epilepsy