Abstracts (HTML) List of Authors

Saffari, Afshin

P 705. Axenfeld-Rieger Anomaly and Neuropsychiatric Symptoms

Saft, Carsten

P 329. Patients with Juvenile Huntington’s Disease Benefit from Early Diagnosis

Sánchez-Albisua, Iciar

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

Sarpong-Bengelsdorf, Akosua

P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 468. Clinical Phenotype of Cerebral Palsy Depending on the Cause
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy

Schallner, Jens

P 522. Measuring Grip and Finger Flexion Strength in Children and Adolescents with Neuromuscular Disorders
P 370. Establishing Anthropometric Parameters and Strength Parameters of the Hand and Arm—Standard Values for Pediatric Neurorehabilitation

Schanda, Kathrin

P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents

Schara, Ulrike

P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
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 409. The Noonan’s Syndrome as a Differential Diagnosis of a Congenital Myasthenic Syndrome
P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries
P 307. Walker–Warburg’s Syndrome Due to Homozygous POMK Mutation in Preterm Twins: Case Report

Schiergens, Katharina A.

FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1

Schipper, Birgit

P 1155. Focal Epilepsy Difficult to Treat in Hermann–Pallister’s Syndrome (KBG Syndrome)

Schmid, Karoline

FV 798. Neurofeedback Therapy for ADDH: Training with z-scored QEEG-Frequency Bands

Schmid, Ulrich

FV 798. Neurofeedback Therapy for ADDH: Training with z-scored QEEG-Frequency Bands

Schmidt, Martina

P 1014. Neurodevelopmental Outcome in VLWB Preterm Infants with Neonatal Seizures Born between 2008 and 2011 at the Age of 2 Years

Schmidt, Nele Kaline

P 336. Unusual Manifestation of Lyme Neuroborreliosis in Childhood and Adolescence

Schnabel, Sabrina

FV 918. How Do Pediatricians and General Practitioners Deal with Epilepsy Patients? Results of a Structured Interview

Schneider, Joanna

FV 757. Clinical, Radiological and Genetic Spectrum of a Large Pediatric Cohort with Epilepsy
P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 468. Clinical Phenotype of Cerebral Palsy Depending on the Cause
P 451. Clinical Presentation of Children and Adolescents with Neurofibromatosis Type I
P 648. The Influence of Secondary Untethering on Bladder Function of Spina Bifida Patients
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy
P 773. Standard Values for Cranial Magnetic Resonance Imaging in the First Year of Life

Schnittert-Hübener, Sarah

P 973. Case Report of a 13-Year-Old Boy with Multiple Sclerosis and Obesity Caused by a MC4-Receptor Mutation

Schnur, Rhonda

FV 241. Mutations in NFE2L2 Lead to a Novel Treatable Neurological Disorder with Leukoencephalopathy

Schoening, Stefan

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

Scholl-Buergi, Sabine

P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland

Schöne-Bake, Jan-Christoph

P 411. GNAO1-Associated Hyperkinetic-Dystonic Movement Disorder and Developmental Delay in a 14-Year-Old Girl

Schönfeld, Brigitte

P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?

Schöning, Martin

FV 449. Cerebral Blood Flow Volume and Gray Matter Volume across a Wide Age Range

Schorling, David

FV 880. Disorders of Coagulation in Duchenne Muscular Dystrophy?—Results of a Registry-Based Online Questionnaire

Schriever, Valentin

FV 606. Untersuchungen von Riechtraining auf die olfaktorische Funktion und kognitive Leistung nach Schädel-Hirn-Trauma im Kindesalter
P 379. Objective Assessment of Central Nervous Odor Processing in Infancy

Schröder, Sebastian

FV 318. Infant Automated Motion Recognition Technology Using RGB-Depth Sensors for Markerless, Rater-Independent Detection of Abnormal Movements in Early Infancy—In a Motion Project
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
P 913. Heterozygous Nonsense Variant in the TCF20 Gene as a Cause of Congenital Myopathy
FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017

Schröder, Simone

FV 1118. The Acquisition of Rare Neurological Disorders in Childhood (“ESNEK”)—Interim Results after 4 Years

Schubert-Bast, Susanne

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

Schuelke, Markus

P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype

Schuler, Heike

FV 658. Cognitive Impairment, Depression, Fatigue, and Quality of Life in Pediatric-Onset Multiple Sclerosis: Results of the Multiple Sclerosis Inventory of Cognition in ADOlescents Study

Schülke, Markus

FV 563. Frequency and Relevance of Neuronal Autoantibodies in Childhood Neurological Disorders

Schülke-Gerstenfeld, Markus

P 334. Severe Leigh-like Phenotype in an Girl with Homozygous p.Q139* Mutation in C12orf65

Schultze-Rhonhof, Mira

FV 747. Early-Onset Progressive Dystonia in Childhood with New Mutations in KMT2B

Schulz, Angela

FV 1180. The Unified Batten Disease Rating Scale: An International Collaboration Testing Validation and Reliability in an Independent Cohort of CLN3-Patients
FV 1182. Ataxia and/or Language Regression at Early School Age—Think of Atypical CLN2 Disease
FV 1181. Intracerebroventricular Drug Delivery for CLN2 Disease—5 Years of Experience with ICV Enzyme Replacement Therapy in Hamburg
FV 1183. Long-Term Safety and Efficacy of Intraventricular Enzyme Replacement Therapy in CLN2 Disease: 2-Year Results from an Ongoing Multicenter Extension Study

Schulz, Anne

FV 318. Infant Automated Motion Recognition Technology Using RGB-Depth Sensors for Markerless, Rater-Independent Detection of Abnormal Movements in Early Infancy—In a Motion Project

Schulz, Matthias

P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy

Schulze, Johannes

P 1092. The Challenging Nature of Cerebral TBC Manifestations in Children and Young Adults
P 1103. Fatal Outcome of Metapneumovirus Infection in Patient with 4H Syndrome

Schulze-Bonhage, Andreas

FV 269. Cannabidiol for Treatment of Childhood Epilepsy—A Cross-Sectional Survey

Schulz-Heise, Susanne

P 1008. Neuronal Migration Disorders in Infants with 22q11.2 Deletion Syndrome—Two Case Reports

Schwabe, Katharina

FV 606. Untersuchungen von Riechtraining auf die olfaktorische Funktion und kognitive Leistung nach Schädel-Hirn-Trauma im Kindesalter

Schwalb, Sonja

P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy

Schwartz, Oliver

FV 837. Early Withdrawal of Antiepileptic Medication in Patients with Juvenile Myoclonic Epilepsy Is Justifiable!
FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?
FV 1178. The More the Merrier? Diagnostic Yield of EEG after the First Unprovoked Seizure
P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy
P 967. IRIS—A Dreaded Complication of Tuberculous Meningitis
P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings

Schwarz, Oliver

FV 1177. Genetic Causes of Congenital Hydrocephalus

Schweiger, Bernd

P 307. Walker–Warburg’s Syndrome Due to Homozygous POMK Mutation in Preterm Twins: Case Report

Schwering, Christoph

FV 1180. The Unified Batten Disease Rating Scale: An International Collaboration Testing Validation and Reliability in an Independent Cohort of CLN3-Patients
FV 1182. Ataxia and/or Language Regression at Early School Age—Think of Atypical CLN2 Disease
FV 1181. Intracerebroventricular Drug Delivery for CLN2 Disease—5 Years of Experience with ICV Enzyme Replacement Therapy in Hamburg

Schwerin-Nagel, Anette

P 1030. MRI Pattern in Neurodegeneration with Brain Iron Accumulation and Fucosidosis Appear Similar

Schwersenz, Inge

P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries

Seidel, Meike

FV 695. Does Early Postnatal hCMV Infection Have Long-Term Consequences on Brain Structure of Former Preterm Born Children?

Seidel, Ulrich

FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
P 973. Case Report of a 13-Year-Old Boy with Multiple Sclerosis and Obesity Caused by a MC4-Receptor Mutation
P 648. The Influence of Secondary Untethering on Bladder Function of Spina Bifida Patients

Seidl, Rainer

FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome

Sekarski, Nicole

FV 571. Cardiac Kids with Stroke

Serino, Domenico

P 366. 7q11.23 Microduplication Syndrome: Neurophysiological and Neuroradiological Insights into a Rare Chromosomal Disorder

Shell, Richard

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

Siebner, Hartwig

FV 588. Probing Homeostatic and Metaplastic Mechanisms of Synaptic Plasticity in Human Primary Motor Cortex Using High-Frequent Quadri-pulse Theta Burst Stimulation

Sinningen, Kathrin

P 235. Short-Term Effects of Lunch with Varying Glycemic Index on Children’s Cognitive Function—CogniDo GI-II

Slasor, Peter

FV 1183. Long-Term Safety and Efficacy of Intraventricular Enzyme Replacement Therapy in CLN2 Disease: 2-Year Results from an Ongoing Multicenter Extension Study

Slavova, Nedelina

FV 513. A Potential Risk of Inadequate Prognosis in Hypothermic Children after Asphyxia with Delayed Abnormalities in Diffusion-Weighted Images

Smith, Laurie D.

P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype

Sommerville, Kenneth

IP 112. Cannabidiol Treatment Effect and Adverse Events in Patients with Lennox–Gastaut’s syndrome: Pooled Results from Two Trials

Sorantin, Erich

P 788. MOG-Ab Positive Acute Disseminated Encephalomyelitis with Asymmetric Lesions in Basal Ganglia and in Thalami
P 1030. MRI Pattern in Neurodegeneration with Brain Iron Accumulation and Fucosidosis Appear Similar

Specchio, Nicola

FV 1183. Long-Term Safety and Efficacy of Intraventricular Enzyme Replacement Therapy in CLN2 Disease: 2-Year Results from an Ongoing Multicenter Extension Study

Spiegler, Juliane

FV 1170. What Influences Motor Function in VLBW Preterm at 5 Years of Age?
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland

Spors, Birgit

P 773. Standard Values for Cranial Magnetic Resonance Imaging in the First Year of Life

Sproule, Douglas M.

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

Stahl, Anna

P 329. Patients with Juvenile Huntington’s Disease Benefit from Early Diagnosis

Stark, G. Björn

FV 947. What, When, and for Whom?—Reconstructive Surgery for Congenital Complete and Partial Facial Palsy

Stark, Wiebke

FV 1119. Incidence of Epilepsies and Epileptic Syndromes in Children and Adolescents: A Prospective Study in Göttingen, Germany in 2014

Staudt, Martin

P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis

Staufner, Christian

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

Stein, Anja

P 307. Walker–Warburg’s Syndrome Due to Homozygous POMK Mutation in Preterm Twins: Case Report

Steinbrücker, Katja

P 1081. PTEN-Associated Macrocephaly in a 3-Year-Old Girl

Steinert, Martin

P 1032. Cognitive Development in Children with Rolandic Epilepsy or Rolandic EEG Pattern—Preliminary Results of a Prospective Follow-up Study

Steinfeld, Robert

FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1

Steinke-Lange, Verena

P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?

Steinlin, Maja

FV 571. Cardiac Kids with Stroke
FV 513. A Potential Risk of Inadequate Prognosis in Hypothermic Children after Asphyxia with Delayed Abnormalities in Diffusion-Weighted Images

Stephani, Ulrich

P 1176. Unfamiliar Interactions of Antiepileptic Drugs
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial

Stettner, Georg

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

Stichtenoth, Guido

FV 1170. What Influences Motor Function in VLBW Preterm at 5 Years of Age?

Stoltenburg, Corinna

P 882. Four-Level Release (Rideau) and Glucocorticoid Therapy in Patients with DMD—Additive Positive Effect on Ambulation

Storck, Michael

FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?

Straeter, Ronald

P 967. IRIS—A Dreaded Complication of Tuberculous Meningitis

Straub, Beate

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

Strölin, Manuel

FV 948. Diffusion Tensor Imaging Parameters in Metachromatic Leukodystrophy: Biomarkers for Disease Progress and Therapeutically Therapeutic Evaluation

Strom, Tim M.

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

Strotmann, Peter

P 1079. Early Diagnosis of Neuromyelitis Optica Spectrum Disease as a Prerequisite for Optimal Therapy Management—Report of a Case

Sturm, Marc

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

Stüve, Burkhard

P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland

Sullivan, Joseph

IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial

Süßmut, David

P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype

Syrbe, Steffen

P 605. Epileptic Encephalopathy Caused by Mitochondrial MPC-1 Deficiency Can Benefit from Ketogenic Diet—Significance of Early Genetic Testing for a Targeted Therapy
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies
P 705. Axenfeld-Rieger Anomaly and Neuropsychiatric Symptoms
P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases