Abstracts (HTML) Autorenliste

Badura, Katharina

FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 396. Childhood Hemorrhagic Stroke—A 7-Year Single-Center Experience
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
P 1152. Assessment of Therapeutically Guided Serious Gaming from the Point of View of the Treated Children and Adolescents—A Pilot Study

Balci, Meral

P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids

Balg, Stefanie

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

Balmer, Christian

FV 571. Cardiac Kids with Stroke

Baltsavias, Gerasimos

FV 820. Pediatric Moyamoya Angiopathy: A Rapid Progressive Disease in Children < 5 Years of Age

Bamborschke, Daniel

P 1001. A Pathogenic GABRB3 Variant Is Associated with Cleft Palate in a Patient with Epileptic Encephalopathy

Bast, Thomas

FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies

Bauer, Angela

FV 776. sEMG Biofeedback Therapy in Children with Cerebral Palsy

Baumann, Matthias

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

Baumgartner, Matthias R.

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

Baumkötter, Jochen

P 1111. Case Report of a Juvenile Patient with Niemann–Pick’s Disease Type C

Bayram, Dilan

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

Beblo, Skadi

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

Becker, Kerstin

FV 747. Early-Onset Progressive Dystonia in Childhood with New Mutations in KMT2B
P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?

Becker, Lena-Luise

P 306. Role of Cdk5rap2 in Neocortical Development

Beck-Wödl, Stefanie

FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders
P 1155. Focal Epilepsy Difficult to Treat in Hermann–Pallister’s Syndrome (KBG Syndrome)

Beghetti, Maurice

FV 571. Cardiac Kids with Stroke

Begtrup, Amber

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

Behnecke, Anne

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

Bernert, Günther

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

Bernhard, Matthias K.

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

Berry, Katherine

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

Bertsche, Astrid

FV 918. How Do Pediatricians and General Practitioners Deal with Epilepsy Patients? Results of a Structured Interview
FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?
P 1011. Think Unusual—Developmental Delay Plus: Multimodal Diagnosis of Menkes’ Syndrome

Bertsche, Thilo

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

Berweck, Steffen

FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis
P 1152. Assessment of Therapeutically Guided Serious Gaming from the Point of View of the Treated Children and Adolescents—A Pilot Study

Beschle, Judith

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

Bettendorf, Markus

P 780. Misdiagnosis of Child Abuse—Fibrodysplasia Ossificans Progressiva as a Therapy-Relevant Differential Diagnosis in Infancy

Betzler, Cornelia

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

Beyerlein, Andreas

FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies

Bhathal, Hari

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

Bien, Christian G.

P 556. Ketogenic Dietary Therapies—Retrospective Assessment of 143 Children Treated at the Bethel Epilepsy Center from 2003 to 2016

Bigi, Sandra

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

Biskup, Saskia

P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy
P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings

Blakely, Emma

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

Blankenburg, Markus

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

Blaschek, Astrid

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 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
P 913. Heterozygous Nonsense Variant in the TCF20 Gene as a Cause of Congenital Myopathy

Bluemchen, Katharina

P 1092. The Challenging Nature of Cerebral TBC Manifestations in Children and Young Adults

Bodensteiner, Christoph

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

Boie, G.

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

Boltshauser, Eugen

P 295. Everolimus Trial for a Patient with Bannayan–Riley–Ruvalcaba’s Syndrome and Progressive Lipomatosis

Bonfert, Michaela Veronika

FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 396. Childhood Hemorrhagic Stroke—A 7-Year Single-Center Experience
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017

Bonnen, Penelope

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

Borell, Sabine

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

Borggräfe, Ingo

FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
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
FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017

Bornheimer, Annalena

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

Bösing, Hendrik

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

Boy, Nikolas

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

Brämswig, Nuria

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

Brand, Joerg

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

Brandl, Ulrich

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

Brenner, Sebastian

P 916. Lissencephaly and Prolonged Survival of a Male Infant with MICPCH and a Noval Mutation in the CASK Gene, Xp11.4

Brentrup, Angela

FV 1177. Genetic Causes of Congenital Hydrocephalus

Breu, Markus

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

Breuer, Anna Sophie

P 379. Objective Assessment of Central Nervous Odor Processing in Infancy

Brockmann, Knut

FV 1119. Incidence of Epilepsies and Epileptic Syndromes in Children and Adolescents: A Prospective Study in Göttingen, Germany in 2014
FV 1118. The Acquisition of Rare Neurological Disorders in Childhood (“ESNEK”)—Interim Results after 4 Years

Broser, Philip

P 1166. Isolated Oculomotor Nerve Palsy as Primary Manifestation of Guillain–Barré’s Syndrome—A Case Report with Focus on Clinical and Electrophysiological Features

Broser, Philip Julian

FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children
FV 113. Electrophysiological Diagnostic of Neuromuscular Diseases in Newborns, Infants, and Toddlers

Brösse, Ines

P 694. TRIP12 Variants as a Cause of Mental Disability with or without Autism

Brotschi, Barbara

FV 571. Cardiac Kids with Stroke

Brunner-Kainz, Michaela

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

Buchert, Rebecca

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

Buchert-Lo, Rebecca

P 968. Vitamine B6-Dependent Epilepsy in a 14-Year-Old Girl with Drug-Resistant Seizures and Recurring Status Epilepticus

Buelow, Markus

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

Buerki, Sarah

FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children

Burdach, Stefan

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

Burghes, Arthur H. M.

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