Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Wagentristl, HP

Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation

Wagner, M

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results

Wallis, J

Contactin-associated protein-like 2 antibodies (CASPR2) encephalopathy in 3-year-old dizygotic twins

Walsh, S

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Walther, A

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Waltz, S

Nicolaides-Baraitser Syndrome

Wanschitz, J

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Warken, B

Which covariates influence effectiveness of intensified robotic-assisted treadmill therapy in children with cerebral palsy

Warmuth-Metz, M

Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports

Weber, K

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Weber, Y

Ocular myositis

Wegendt, C

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Wehrmann, C

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Wei, XC

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum
Hemimegalencephaly: involvement of cranial nerves and intracranial vessels

Weigt-Usinger, K

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt
Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)
A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography
Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency
Visual impairment – differential diagnoses

Weis, J

Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt
Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Weissensteiner, M

Kernicterus: a case study

Werneck, H

Quality of life and mental health of neuropediatric patients

Wickede, M von

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Wiegand, G

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Wieland, T

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Wiemer-Kruel, A

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?
Panic attacks in girls with double cortex syndrome: ictal amaurosis

Wiesinger-Eidenberger, G

Kernicterus: a case study

Wilichowski, E

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription
Divergence in clinical presentation of Dynamin2-caused centronuclear myopathy is associated with mutations in distinct parts of the DNM2 gene
Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype

Wilke, M

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents
Interhemispheric connectivity in congenital hemiparesis

Will, B

Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Wille, DA

Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene

Winkler, A

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Witsch-Baumgartner, M

Weakness of the limb girdle type with finger tremor and elevated creatine kinase

Witt, O

Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?

Wittig, I

The German network for mitochondrial disorders (mitoNET)

Wohlrab, G

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings
Myoclonic epilepsy as affection of central nervous system in Farber disease

Wolf, N

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
PNPO mutations in patients with pyridoxine dependent epilepsy

Wolf, P

Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency
Acute hemiataxia in childhood

Wolff, M

Early childhood onset progressive myoclonic epilepsy phenotype caused by KCTD7 mutations
Lambdoid synostosis or positional plagiocephaly – a visual diagnosis?

Würfel, E

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis

Würfel, J

Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis