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

Abstracts (HTML) List of Authors

Radke, I

Fibroadenoma under therapy with interferons in multiple sclerosis

Rahbek, J

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Ramberger, M

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Ramisch, EM

Dramatic neurological signs in children with intussusception

Rating, D

Refractory epilepsy in a patient with Doose syndrome: favorable response after add-on therapy with bromide

Rauch, A

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
Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich

Rauchenzauner, M

Activities of daily living in children with hemiparesis: Influence of cognitive functions and motor competence on quality of performance

Rauscher, C

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

Razmdjou, S

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Reichenbach, JR

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Reihle, C

Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation

Reimnitz, D

Hereditary congenital mirror movements

Reindl, M

N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases

Reinhard, RW

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

Reis, A

Nicolaides-Baraitser Syndrome

Rensing-Zimmermann, C

Bone health and vitamin D metabolism in children and adolescents with Duchenne muscular dystrophy compared with other neuromuscular diseases and cerebral palsy

Rettinger, N

Case report: oculomotor apraxia in ataxia telangiectasia

Reuner, G

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems

Reutlinger, C

Dysphagia following implantation of an vagus nerve stimulator – a case report

Riccabona, M

PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone
Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Richter, G

Acute hemiataxia in childhood

Richter, M

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment

Rieß, A

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Ring, E

Tuberous sclerosis complex-successful therapy with everolimus

Röder, B

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Rodger, S

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Rödiger, M

Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia

Rödl, T

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Rohrbach, M

Myoclonic epilepsy as affection of central nervous system in Farber disease

Ros Cervera, G

Neurological symptoms and demyelinating changes on MRI at 3 brothers with cryopyrin-associated periodic syndrome

Rosewich, H

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders
Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Rossegg, U

Kernicterus: a case study
Transverse myelitis versus encephalitis disseminata
Paroxysmal kinesogenic dyskinesia
Congenital myasthenic syndromes: a difficult approach to diagnosis and therapy
13-year-old patient with headache, unclear on/off symptoms and psychosocial burden
Ischemic Stroke in a 14-year-old Boy with Homozygous C677T MTHFR Mutation

Rost, I

Heterozygous deletion of exon 3 of phospholipase C β1 gene causes neonatal epileptic encephalopathy?

Rostásy, K

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism
Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis
Neuropsychological long-term outcome in children with SVT
Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings
Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum
Epileptic seizures and chromosomal microdeletions/duplications
Visual disorders in children with cerebral palsy
Epilepsy in children with cerebral palsy
Central nervous system demyelination complicating Guillain-Barré syndrome
Jeavon syndrome as a differential diagnosis of facial tics
Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease
Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years
N-Methyl-D-Aspartate Receptor Antibodies in Neuroinflammatory Diseases
Editorial

Rötig, A

Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing

Rückriegel, S

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Rudnik-Schöneborn, S

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Ruf, S

Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations