Abstracts (HTML) List of Authors

Haack, Tobias

FV 735. UBTF-Related Dementia and Parkinsonism—Case Report of a Novel Disease Entity
FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders
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
P 968. Vitamine B6-Dependent Epilepsy in a 14-Year-Old Girl with Drug-Resistant Seizures and Recurring Status Epilepticus
P 1030. MRI Pattern in Neurodegeneration with Brain Iron Accumulation and Fucosidosis Appear Similar

Haas, Carola A.

P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies

Haas, Dorothea

P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases

Haber, Benjamin

P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases

Häberle, Johannes

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

Hackenberg, Annette

FV 735. UBTF-Related Dementia and Parkinsonism—Case Report of a Novel Disease Entity
FV 571. Cardiac Kids with Stroke
FV 820. Pediatric Moyamoya Angiopathy: A Rapid Progressive Disease in Children < 5 Years of Age

Hagberg, Gisela

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

Hahn, Gabriele

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

Haidich, Anna-Bettina

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

Halimeh, Susan

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

Hanebeck, Benjamin

P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases

Harmsen, Stefani

P 1164. Pre-wallerian Degeneration versus New Ischemic Infarction

Harting, Inga

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

Hartmann, Hans

P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
P 411. GNAO1-Associated Hyperkinetic-Dystonic Movement Disorder and Developmental Delay in a 14-Year-Old Girl

Hasselmann, Oswald

FV 113. Electrophysiological Diagnostic of Neuromuscular Diseases in Newborns, Infants, and Toddlers

Hauenstein, Christina

P 1011. Think Unusual—Developmental Delay Plus: Multimodal Diagnosis of Menkes’ Syndrome

Hauser, Till-Karsten

FV 695. Does Early Postnatal hCMV Infection Have Long-Term Consequences on Brain Structure of Former Preterm Born Children?
FV 930. Reduced Structural Connectivity in Nonmotor Networks in Children Born Preterm

Hehr, Ute

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

Heinen, Florian

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 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

Heller, Corina

P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings

Helling-Bakki, Astrid

P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases

Hennes, Eva-Maria

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

Hennig, Bert

FV 571. Cardiac Kids with Stroke

Henrich, Maria

P 409. The Noonan’s Syndrome as a Differential Diagnosis of a Congenital Myasthenic Syndrome

Hentschel, Franziska

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

Henzi, Bettina

FV 571. Cardiac Kids with Stroke

Herberhold, Thomas

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

Heringer, Jana

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

Herkenrath, Peter

P 613. IQSEC2-Associated X-Coupled Mental Retardation 1 in a Girl with Difficult-to-Treat Epilepsy
P 1001. A Pathogenic GABRB3 Variant Is Associated with Cleft Palate in a Patient with Epileptic Encephalopathy

Hermann, Katharina

P 1147. Pyridostigmine Leads to Relevant Improvement of Motor Function in an Infant with RYR1-Related Congenital Myopathy

Hermann-Alves, Sofia

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

Hernandez-Miranda, Luis Rodrigo

P 1086. Role of PTRH2 in Cerebellar Development

Herting, Arne

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

Herting, Egbert

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

Hesse, Nikolas

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

Hethey, Sven

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

Heußinger, Nicole

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

Heyer, Christoph

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

Hildebrandt, Martin

P 518. Vitamin B6-Dependent West’s Syndrome: An Unexplained Case

Hillenbrand, Nikolas

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

Himes, Ryan

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

Hinze, Claas

P 967. IRIS—A Dreaded Complication of Tuberculous Meningitis

Hobbiebrunken, Elke

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

Hoffjan, Sabine

P 564. Psychosocial Surrounding as an Important Influencing Factor with Hereditary Sensory and Autonomic Neuropathy—Two Case Reports

Hoffmann, Florian

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

Hoffmann, Georg F.

FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
P 605. Epileptic Encephalopathy Caused by Mitochondrial MPC-1 Deficiency Can Benefit from Ketogenic Diet—Significance of Early Genetic Testing for a Targeted Therapy

Hoffmann, Georg Friedrich

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
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
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies
P 694. TRIP12 Variants as a Cause of Mental Disability with or without Autism
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
P 780. Misdiagnosis of Child Abuse—Fibrodysplasia Ossificans Progressiva as a Therapy-Relevant Differential Diagnosis in Infancy

Hofmann-Peters, Anne

P 556. Ketogenic Dietary Therapies—Retrospective Assessment of 143 Children Treated at the Bethel Epilepsy Center from 2003 to 2016
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland

Hofstetter, Peter

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

Holinski-Feder, Elke

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

Holz, Anja

P 613. IQSEC2-Associated X-Coupled Mental Retardation 1 in a Girl with Difficult-to-Treat Epilepsy

Horn, Annette

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

Hörtnagel, Konstanze

P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy

Hu, Hao

P 1086. Role of PTRH2 in Cerebellar Development

Hug, Maja

FV 571. Cardiac Kids with Stroke

Hunkemöller, Franziska

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

Huppke, Brenda

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

Huppke, Peter

FV 241. Mutations in NFE2L2 Lead to a Novel Treatable Neurological Disorder with Leukoencephalopathy
P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids

Husain, Ralf

FV 188. Morbus Krabbe: One disease—Two Faces
P 366. 7q11.23 Microduplication Syndrome: Neurophysiological and Neuroradiological Insights into a Rare Chromosomal Disorder

Hustedt, Ulf

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