Abstracts (HTML) List of Authors

Kaindl, Angela

FV 563. Frequency and Relevance of Neuronal Autoantibodies in Childhood Neurological Disorders
P 451. Clinical Presentation of Children and Adolescents with Neurofibromatosis Type I

Kaindl, Angela M.

FV 757. Clinical, Radiological and Genetic Spectrum of a Large Pediatric Cohort with Epilepsy
P 306. Role of Cdk5rap2 in Neocortical Development
P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 468. Clinical Phenotype of Cerebral Palsy Depending on the Cause
P 1086. Role of PTRH2 in Cerebellar Development
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
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

Kaiser, Ann-Sophie

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

Kalbe, Elke

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

Kalyvas, C.

IP 467. Botulinum Toxin Type A in the Management of Spasticity in Children—A Systematic Literature Review and Bayesian Network Meta-analysis

Kampmann, Christoph

P 1106. Involvement of the Cardial Autonomous Nervous System in Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Kansu, Aydan

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

Kappert, Günther

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

Kappl, Simon

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

Karabis, A.

IP 467. Botulinum Toxin Type A in the Management of Spasticity in Children—A Systematic Literature Review and Bayesian Network Meta-analysis

Karenfort, Michael

FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
P 1168. Management of Highly Active MS in Children: Successful Early Escalation Therapy with Alemtuzumab

Kaspar, Brian K.

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

Kehrer, Christiane

FV 300. Living with Severe Rare Chronic Neurological Disease in Childhood: Family Burden and Quality of Life in Families with MLD and PCH2
FV 188. Morbus Krabbe: One disease—Two Faces
FV 948. Diffusion Tensor Imaging Parameters in Metachromatic Leukodystrophy: Biomarkers for Disease Progress and Therapeutically Therapeutic Evaluation

Kehrer, Martin

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

Kersting, Mathilde

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

Kessler, Josef

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

Khan, Nadia

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

Kiefer, Petra

FV 953. Parents’ Experiences during the Compassionate Use Program (Nusinersen) for Patients with Spinal Muscular Atrophy Type 1—A Qualitative Interview Study

Kiening, Karl

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

Kieslich, Matthias

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
P 587. Osmotic Myelinolysis—A Rare but Severe Complication of Diabetic Ketoacidosis

Kiess, Wieland

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

Kirschner, Janbernd

FV 880. Disorders of Coagulation in Duchenne Muscular Dystrophy?—Results of a Registry-Based Online Questionnaire
FV 953. Parents’ Experiences during the Compassionate Use Program (Nusinersen) for Patients with Spinal Muscular Atrophy Type 1—A Qualitative Interview Study
P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries
P 900. Decision Making Regarding Ventilator Support in Children with SMA type 1—A Cross-sectional Survey among German Physicians

Kissel, John T.

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

Kiwull, Lorenz

P 1152. Assessment of Therapeutically Guided Serious Gaming from the Point of View of the Treated Children and Adolescents—A Pilot Study

Klabunde-Cherwon, Annick

P 605. Epileptic Encephalopathy Caused by Mitochondrial MPC-1 Deficiency Can Benefit from Ketogenic Diet—Significance of Early Genetic Testing for a Targeted Therapy

Klepper, Jörg

FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
FV 236. Twenty-five Years Glut1 Deficiency in Neuropediatrics—The Importance for Adult Neurology

Klose, Uwe

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

Kloss, Manja

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

Kloth, Katja

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

Klotz, Alexandra

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

Kluger, Gerhard

P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial

Knieling, Ferdinand

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

Knieriem, Ellen

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

Knierim, Ellen

FV 563. Frequency and Relevance of Neuronal Autoantibodies in Childhood Neurological Disorders
P 973. Case Report of a 13-Year-Old Boy with Multiple Sclerosis and Obesity Caused by a MC4-Receptor Mutation
P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype

Knuf, Markus

P 1106. Involvement of the Cardial Autonomous Nervous System in Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Kochan, Aleksandra

FV 757. Clinical, Radiological and Genetic Spectrum of a Large Pediatric Cohort with Epilepsy

Koch-Hogrebe, Margret

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

Köhler, Cornelia

P 1032. Cognitive Development in Children with Rolandic Epilepsy or Rolandic EEG Pattern—Preliminary Results of a Prospective Follow-up Study
P 564. Psychosocial Surrounding as an Important Influencing Factor with Hereditary Sensory and Autonomic Neuropathy—Two Case Reports
P 326. Developments in Stem Cell Transplantation in Lysosomal Storage Diseases—An Update on the Example of Mucopolysaccharidoses

Köhler, Jutta

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

Koitschev, Assen

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

Kölbel, Heike

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

Kölker, Stefan

FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
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 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 694. TRIP12 Variants as a Cause of Mental Disability with or without Autism
P 705. Axenfeld-Rieger Anomaly and Neuropsychiatric Symptoms
P 780. Misdiagnosis of Child Abuse—Fibrodysplasia Ossificans Progressiva as a Therapy-Relevant Differential Diagnosis in Infancy

Korenke, Georg-Christoph

FV 205. Parkinsonism after Coxsackievirus B3 Brain Stem Encephalitis

Kotzaeridou, Urania

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

Kovacs-Nagy, Reka

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

Kowald, Tobias

FV 205. Parkinsonism after Coxsackievirus B3 Brain Stem Encephalitis

Koy, Anne

FV 747. Early-Onset Progressive Dystonia in Childhood with New Mutations in KMT2B
P 613. IQSEC2-Associated X-Coupled Mental Retardation 1 in a Girl with Difficult-to-Treat Epilepsy

Kraemer, Nadine

P 306. Role of Cdk5rap2 in Neocortical Development

Krägeloh-Mann, Ingeborg

P 968. Vitamine B6-Dependent Epilepsy in a 14-Year-Old Girl with Drug-Resistant Seizures and Recurring Status Epilepticus
FV 300. Living with Severe Rare Chronic Neurological Disease in Childhood: Family Burden and Quality of Life in Families with MLD and PCH2
FV 188. Morbus Krabbe: One disease—Two Faces
FV 948. Diffusion Tensor Imaging Parameters in Metachromatic Leukodystrophy: Biomarkers for Disease Progress and Therapeutically Therapeutic Evaluation

Krämer, Nadine

P 1086. Role of PTRH2 in Cerebellar Development

Kranz, Katharina

P 326. Developments in Stem Cell Transplantation in Lysosomal Storage Diseases—An Update on the Example of Mucopolysaccharidoses

Kraus, Verena

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

Krause, Gudrun

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

Krauspe, Rüdiger

P 232. Interdisciplinary Consensus on Prevention and Therapy of Hip Lateralization in Patients with Cerebral Palsy

Krenn, Larissa

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

Krieg, Sarah

FV 188. Morbus Krabbe: One disease—Two Faces

Kriegesmann-Loke, Antje

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

Krois-Neudenberger, Jana

FV 837. Early Withdrawal of Antiepileptic Medication in Patients with Juvenile Myoclonic Epilepsy Is Justifiable!

Kröll-Seger, Judith

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

Krusen, Martina

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

Küchler, Alma

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

Kudernatsch, Manfred

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

Kühle, Hans-Jürgen

P 327. Is Video-Assisted Methylphenidate Dose Finding for Children with ADHD a Suitable Procedure for Medical Practitioners?—Results after 4-Year-Follow-up

Kuhn, Marius

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

Kühn-Velten, Nikolaus

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

Kuloğlu, Zarife

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

Kurlemann, Gerhard

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

Kurnik, Karin

FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017

Kutschke, Georg

P 1106. Involvement of the Cardial Autonomous Nervous System in Mitochondrial Neurogastrointestinal Encephalopathy Syndrome