Abstracts (HTML) List of Authors

Rabenau, Holger

P 1103. Fatal Outcome of Metapneumovirus Infection in Patient with 4H Syndrome

Ranucci, Giusy

FV 697. Biallelic Mutations in SCYL1 Cause CALFAN-Syndrome (Cholestasis, Acute Liver Failure, and Neurodegeneration), A Congenital Disorder of Intracellular Trafficking with a Variable Neurological Phenotype

Rauh, M.

FV 1091. C1-esterase Inhibitor Treatment Prevents Blood–Brain Barrier Dysfunction in the Neonatal Mouse Brain after Acute Systemic Hypoxia

Redyk, Katharina

FV 205. Parkinsonism after Coxsackievirus B3 Brain Stem Encephalitis

Regényi, Mária

FV 571. Cardiac Kids with Stroke

Reihle, Christof

P 1139. Gradenigo’s Syndrome: Two New Case Studies

Reindl, Markus

FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents

Reinersmann, Annika

FV 969. Transplantation Surgery Used Autologous Transgenic Keratinocyte Cultures Which Regenerated an Entire, Fully Functional Epidermis

Reiter, Karl

FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community

Reutlinger, Constanze

FV 840. Communication Possibilities for Girls with Rett’s Syndrome

Ries, Markus

P 781. A Cross-sectional Quantitative Analysis of the Natural History of Farber Disease: An Ultra-Orphan Condition with Rheumatologic and Neurological Cardinal Disease Features

Rieß, Olaf

FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders

Rimensberger, Peter

FV 571. Cardiac Kids with Stroke

Roberts, Claire

IP 112. Cannabidiol Treatment Effect and Adverse Events in Patients with Lennox–Gastaut’s syndrome: Pooled Results from Two Trials
IP 110. Maintenance of Long-Term Safety and Efficacy of Cannabidiol Treatment in Dravet’s Syndrome: Results of an Open-Label Extension Trial (GWPCARE5)

Rodino-Klapac, Louise

IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones

Rödl, Siegfried

P 788. MOG-Ab Positive Acute Disseminated Encephalomyelitis with Asymmetric Lesions in Basal Ganglia and in Thalami

Rompel, Oliver

P 1081. PTEN-Associated Macrocephaly in a 3-Year-Old Girl
P 1077. Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL): A Case Report

Rossler, Leo

P 736. Benign Enlargement of Subarachnideal Spaces and Subdural Hematoma in an Infant: Spontaneous Bleeding, Child Abuse, or Bleeding Disorder?

Rostasy, Kevin

FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents
P 336. Unusual Manifestation of Lyme Neuroborreliosis in Childhood and Adolescence
P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids

Rostásy, Kevin

P 1151. A 19-Month-Old Boy with Mild Epileptic Encephalopathy and Mutation in the SZT2 Gene

Rothoeft, Tobias

FV 969. Transplantation Surgery Used Autologous Transgenic Keratinocyte Cultures Which Regenerated an Entire, Fully Functional Epidermis

Rupprich, Katrin

P 308. Autosomal Recessive Mutations in the NALCN Gene: A Rare Cause of a Severe Developmental Disorder with Facial Dysmorphia, Epilepsy and Cheyne–Stokes/Biot’s Respiration with Central Apneas
P 307. Walker–Warburg’s Syndrome Due to Homozygous POMK Mutation in Preterm Twins: Case Report

Rüsch, Christina

P 233. Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative Disorder

Ryczek, Monika

P 451. Clinical Presentation of Children and Adolescents with Neurofibromatosis Type I