Abstracts (HTML) List of Authors

Kaindl, A.

Dilatative Cardiomyopathy and Severe Cardiac Dysfunction in a Patient with CCFDN Syndrome
Radiological Changes in Patients with Spina Bifida

Kaindl, A. M.

Pathological Fractures in Patients with Myelomeningocele
Centrosomes, Cilia, and Microcephaly
Lacosamide Lowers Valproate and Levetiracetam Levels

Kaiser, N.

“Porphyria Plus”: Siblings with Homozygous Variegate Porphyria, a Complex Developmental Disorder and Hypomyelination

Kaiser, O.

A Rare Cause of Congenital Ptosis with External Ophthalmoplegia: Case Report and Differential Diagnosis

Kappl, S.

Development of a Classification System for Wheelchair Maintenance and Seat Positioning
A Technical Neuro-Orthopedic and Neuropediatric Report on Requirements Needed for a Successful Rehabilitation of a Disabled Adolescent
Improving the Quality of Care in the Specialization: The Benefits of “Hands-on” Courses for Learning Neuromuscular Ultrasound

Karabul, N.

Globotriaosylsphingosine (Lyso-GB3 bzw. Lyso-GL3), an Excellent Biomarker for Children with Fabry Disease

Karenfort, M.

GAD65-Positive Limbic Encephalitis and Large Temporal Arachnoid Cyst: A Diagnostic Conundrum

Kasprzak, B.

Midaortic Syndrome in TSC

Kauffmann, B.

Everolimus as a Therapy of a Benign, Infiltrative Growing Bone Tumor of the Mandibula: A Rare Manifestation with Tuberous Sclerosis

Kaulisch, M.

FOXG1 Syndrome: Genotype–Phenotype Association in 84 Patients with FOXG1 Variants

Kayacelebi, A. A.

The L-Arginine/NO Pathway in Children with Attention-Deficit/Hyperactivity Disorder (ADHD)

Kehrer, C.

Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy

Kehrer, M.

Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes

Keil, A.

Case Report: Gamma-Sarcoglycanopathy Plus RYR1- and TCAP-Mutations: Do Further Mutations Explain Clinical Variations in Phenotypes of Neuromuscular Diseases?

Kellner, E.

“Nora Imaging”: A Web-Based Platform for Medical Imaging

Kersting, M.

Lunch and Cognitive Performance in School Children: The Crossover Intervention Trial CogniDo

Kieslich, M.

Complications and Follow-up in Pediatric Brain Injuries
Posttraumatic Encephalocele as a Rare but Relevant Complication of Frontobasal Fractures
MEF2C Mutations: The Cause of an Epileptic Encephalopathy Syndrome with Pathognomonic Fidgetiness and Myoclonias

Kirsch, A.

Long-Term Outcome after Vegetative State Due to Near-Drowning and Quality of Life of the Families

Kirsch, C.

View of an Affected Mother: Insights into a Life with the Diagnose NCL

Kirschenhofer, S.

Validation of Digital Spiral Analysis in Pediatric Tremor

Kirschner, J.

Single-Center Experience with Intrathecal Administration of Nusinersen in Children with Spinal Muscular Atrophy Type I

Kirschner, Jan

Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study

Klaassen, S.

Dilatative Cardiomyopathy and Severe Cardiac Dysfunction in a Patient with CCFDN Syndrome

Klein, K.-M.

Recommendations for Diagnostic Genetic Testing in Epilepsies

Klein, M.

Midaortic Syndrome in TSC

Klopstock, T.

NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

Kloth, K.

The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf

Klotz, D.

High-Frequency Oscillations in Surface EEG Recorded from Neonates with Perinatally Acquired Hypoxic Ischemic Encephalopathy: A Retrospective Study

Klotz, K. A.

West Syndrome in Hypothalamic Hamartoma: A Rare Clinical Presentation

Kluger, G.

Long-Term Outcome after Vegetative State Due to Near-Drowning and Quality of Life of the Families
GOAL: Gait Outcome Assessment List
Early-Phase Rehabilitation of Children and Adolescents with Chronic Disorders of Consciousness: Standardized, Ability-Based Registration of Remission (RemiPro) Supports Goal-Finding and Establishing a Prognosis

Kluger, G. J.

Recommendations for Diagnostic Genetic Testing in Epilepsies

Knuf, M.

Autoimmunencephalitis and Psychiatric Symptoms: The Example “SREAT”
Health-Related Quality of Life in Children and Adolescents with Spinal Dysraphic Disorders
Two Siblings with D-Bifunctional Protein Deficiency and Unusual Clinical Course

Koch, J.

Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations

Kohler, B.

Northern Epilepsy: Not So Northern Anymore

Köhler, C.

Plasmapheresis as at Treatment Option in Anti-MOG–Related Neurological Disorders with Fulminant Progress
Unexpected Cause of Progressive Decrease in Sensorimotor Function of the Left Leg
CAPOS-Syndrome: A Rare Differential Diagnosis to Friedreich’s Ataxia

Kohlschütter, A.

The Natural History of Canavan Disease: Description of 23 New Cases and Comparison with Literature

Kölbel, H.

Case Report: Gamma-Sarcoglycanopathy Plus RYR1- and TCAP-Mutations: Do Further Mutations Explain Clinical Variations in Phenotypes of Neuromuscular Diseases?
A Rare Cause of Congenital Ptosis with External Ophthalmoplegia: Case Report and Differential Diagnosis

Kölker, S.

Niemann-Pick Type C Disease: A Challenge in Diagnostics, Therapy, and Care for Affected Families
Quantitative Clinical Characteristics of 53 Patients with MPS VII: A Cross-Sectional Analysis

König, H.

GOAL: Gait Outcome Assessment List

König, N.

Effects of Janus Kinase Inhibition in Two Children with Aicardi-Goutières Syndrome

Korenke, C.

Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy

Korinthenberg, R.

Progressive Radial Motor Neuropathy Due to a Perineurioma in an Adolescent Girl: Case Report
Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy
West Syndrome in Hypothalamic Hamartoma: A Rare Clinical Presentation
Supra- and Infratentorial Atrophy with Cortical Blindness Caused by Mutations in SEPSECS: Case Report

Kössler, M.

Neuromyelitis Optica Spectrum Disorders in Pediatric Patients

Kößler, M.

Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck

Kotchoubey, B.

Mythology of the Vegetative State

Koustenis, E.

Motor Function in Pediatric ALL Survivors after Chemotherapy-Only

Krägeloh-Mann, I.

“Porphyria Plus”: Siblings with Homozygous Variegate Porphyria, a Complex Developmental Disorder and Hypomyelination
Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy

Kratz, C.

Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive

Krauser, J.

Expert Opinion on the Management of Intracerebroventricular (ICV) Drug Delivery

Kremer, L.

NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

Kress, W.

Case Report: Gamma-Sarcoglycanopathy Plus RYR1- and TCAP-Mutations: Do Further Mutations Explain Clinical Variations in Phenotypes of Neuromuscular Diseases?

Krestel, S.

“Porphyria Plus”: Siblings with Homozygous Variegate Porphyria, a Complex Developmental Disorder and Hypomyelination

Kroger, H.

Meta-analyses of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial

Krois-Neudenberger, J.

Are Reemergence of Sleep Spindles and Cessation of Hypsarrhythmia Prognostic Factors for Neurodevelopmental Outcome in Adults with a History of West Syndrome in Infancy?

Kröll, J.

Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins

Krumm, A.

Explorative Saccade Training in Children with Homonymous Hemianopia

Kruse, B.

Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis

Kubisch, C.

The Potential of Whole-Exome Sequencing (WES) in Neuropediatric Patients: Single-Center Experience at the University Hospital Hamburg Eppendorf

Kucian, K.

The Importance of Central-Visual Perception Disorders for Dyslexia and Dyscalculia

Kudernatsch, M.

Worsening of Hand Function but Significant Improvement of Abilities Measured in PEDI in a Child with Sturge-Weber Syndrome

Kuhnke, N.

High-Frequency Oscillations in Surface EEG Recorded from Neonates with Perinatally Acquired Hypoxic Ischemic Encephalopathy: A Retrospective Study

Kuntz, N.

Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)

Kuntz, Nancy

Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study

Kunze, F.

What Is the Right Pressure of Shunt Valves in Newborns?

Kunze, S.

Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP

Kurlemann, G.

Unilateral Atrophy of the Tongue: Hypoglossal Palsy Due to Neurovascular Contact?
Midaortic Syndrome in TSC
Are Reemergence of Sleep Spindles and Cessation of Hypsarrhythmia Prognostic Factors for Neurodevelopmental Outcome in Adults with a History of West Syndrome in Infancy?
Forceful Monitoring after Acute Pediatric Stroke Can Help Identify the Etiology
When It Is Not MS…—Differential Diagnosis of Optic Neuritis and Multifocal Inflammatory Cerebral Lesions in an Adolescent
Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation
The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System

Kurth, I.

Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy

Küster, S.

Explorative Saccade Training in Children with Homonymous Hemianopia