Abstracts of the 42nd Annual Meeting of the Society for Neuropediatrics

Abela, L.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Abeln, H.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Abicht, A.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Adler, C.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Ahting, U.

Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Aktas, O.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Alber, M.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Albrecht, B.

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Albrecht, U.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Alhaddad, B.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Alkuraya, F. S.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Althaus, J.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Anastasopoulos, C.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Andres, B.

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Andresen, F.

Rare Case of Miller-Fisher Syndrome

Anlar, B.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Antenbrink, F.

Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler

Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation

Apel, K.

Quantitative Sensory Testing Is Highly Sensitive in Detecting Chemotherapy-Induced Peripheral Neuropathy

Asadollahi, R.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Assing, B.

Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension

Assmann, B.

New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype

Augst, D.

Rhabdomyolysis as a Rare Complication of Diabetic Ketoacidosis in a Twelve-Year-Old Boy

Baethmann, M.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Bähring, R.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Bajer-Kornek, B.

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Ballheimer, Y.

Age-Specific Changes of the AMPA Receptor and ADAR Enzyme Expression Profile in the Neonatal Mouse Brain due to Pilocarpine-Induced Seizures

Balling, G.

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Bartels, F.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Bast, T.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Bauder, F.

Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Baumann, M.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Landau-Kleffner Syndrome (Epileptic Aphasia)

Baumgartner, S.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Baumgartner, Sigl S.

Landau-Kleffner Syndrome (Epileptic Aphasia)

Becher, Th.

Successful Therapy of Holmes Tremor with a Silicone Hand-Wrist Orthesis and Botulinum Toxin A

Trichotillomania under a Therapy with Lisdexamfetamine

Bechtel, N.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Becker, K.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Belke, F.

Rhabdomyolysis as a Rare Complication of Diabetic Ketoacidosis in a Twelve-Year-Old Boy

Benet-Pagès, A.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Berger, T.

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Bernhard, M. K.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Berthold, O.

Hypocalcemic Partial Seizures in the Newborn

Bertsche, A.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Bertsche, T.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Berweck, S.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Muscle-Adaptation in Children with Acquired Brain Injuries

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Beste, C.

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Betzler, C.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Study Group: Personalized Therapy in Rare Pediatric Epilepsies

Beutel, K.

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Beytia, M.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Biebl, A.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Bigi, S.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Blahak, C.

Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy

Blankenburg, M.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2

Quantitative Sensory Testing Is Highly Sensitive in Detecting Chemotherapy-Induced Peripheral Neuropathy

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Symptomkontrolle bei Lebenslimitierenden Neuropädiatrischen Krankheitsbildern

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Blaschek, A.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Bode, H.

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Bönnemann, C.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Bönnemann, C. G.

Congenital Disorders of Muscle: Genes and Mechanisms

Borell, S.

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Borggräfe, I.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Bornemann, A.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Borusiak, P.

Variety of Phenotypes in Chromosome 16p11.2 Deletion Syndrome

Brackmann, F.

Age-Specific Changes of the AMPA Receptor and ADAR Enzyme Expression Profile in the Neonatal Mouse Brain due to Pilocarpine-Induced Seizures

Brand, L.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Brandl, U.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Braun, S.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Braun, Simon

Development and Evaluation of a Computer-Controlled System to Assess Associative Visual Learning and Memory in Zebrafish Larvae

Breu, M.

A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside

Breuer, K.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Brösse, I.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

Everolimus as Targeted mTOR Inhibition in Neonates and Infants with Tuberous Sclerosis

Brunner-Krainz, M.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Buiting, K.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Bulst, S.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Buob, M.

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Burakiewicz, J.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Burdach, S.

Longitudinal Extensive Transverse Myelitis following T-ALL

Burkhardt, L.

Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin

Bürki, S.

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Buschmann, F.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Bushby, K.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Cagnoli, S.

Variety of Phenotypes in Chromosome 16p11.2 Deletion Syndrome

Cahan, H.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Carlsson, G.

Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents

Christen, H. J.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Claßen, M.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Cloppenborg, T.

Seizures after Hemispherectomy: The Role of the Insula

Coci, E. G

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Company, M.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Cordes, I.

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Cordey, A.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Counsell, S.

The Role of MRI on the Neonatal Brain

Courage, C.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Crowther, L.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Darekar, A. A.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

Das, A.

Developmental Profiles of Children with Pyridoxine-Dependent Epilepsy (PDE)

Das, A. M.

Neurocognitive Outcome in Hepatorenal Tyrosinemia

Daseking, M.

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Datta, A.

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Day, J. W.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

De Bock, F.

Participation in Neuropediatric Care

Decker, C.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Dehmel, M.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Della, Marina A.

Tuberculosis Meningitis with Brainstem Mass Lesion—Adjunctive Treatment with Thalidomide: A Case Report

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

de los Reyes, E.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Denecke, J.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Dettmers, S.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Deutz, U.

Case Reports: Intracranial Abscesses

di Donato, N.

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Dieckmann, A.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Dietel, T.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Distelmaier, F.

Rare Causes of Childhood Stroke: A Single-Center Experience

Doering, J.-H.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

Dohna-Schwake, C.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Dörr, H. G.

Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report

Dorsch, V.

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Doummar, D.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Down, M.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Dubern, B.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Dulcey-Husi, A.

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Dünner, C.

In Delayed Myelination Count on T(o)3

Dusl, M.

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Dütting, T.

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Eagle, M.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Eckenweiler, M.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Egger, S.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Ehl, R. S.

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Ehrenmueller, M.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Einspieler, C.

It Is Not Too Early: Clinical Implications of Early Spontaneous Movements

Elfring, G.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Ellenberger, D.

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Elpers, C.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Engeland, B.

The Voltage-Gated Sodium Channel Nav1.2 Contributes to Neurodegeneration in an Animal Model of Multiple Sclerosis

Engert, Florian

Development and Evaluation of a Computer-Controlled System to Assess Associative Visual Learning and Memory in Zebrafish Larvae

Erdlenbruch, B.

A New Mitochondrial tRNA(Met)—Gene Mutation in a 12-Year-Old Boy with MELAS: Clinical Presentation and Effects of Arginine Treatment

Ernemann, U.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Faas, D.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Faqeih, E.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Farr, M.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Fazeli, W.

The Voltage-Gated Sodium Channel Nav1.2 Contributes to Neurodegeneration in an Animal Model of Multiple Sclerosis

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Feder, L.

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Felderhoff-Müser, U.

Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension

Fellner, C. M.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Fellner, F. A.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Fiedler, B.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Fiedler, E.

Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2

Finetti, C.

Rhabdomyolysis as a Rare Complication of Diabetic Ketoacidosis in a Twelve-Year-Old Boy

Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review

Fink, A.

Participation in Neuropediatric Care

Fink, C.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Finke, C.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Finkel, R.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Fischer, M.

Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration

Flanigan, K.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Florian, M.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Fluss, J.

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Foit, N.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Frechinger, B.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Freilinger, M.

A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside

Freisinger, P.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Friede, T.

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Friese, M. A.

The Voltage-Gated Sodium Channel Nav1.2 Contributes to Neurodegeneration in an Animal Model of Multiple Sclerosis

Furthner, D.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Gabriel, S.

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Gärtner, J.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Acute Severe Combined Demyelination: Case Report

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Fingolimod in Highly Active Pediatric Multiple Sclerosis

A New Mitochondrial tRNA(Met)—Gene Mutation in a 12-Year-Old Boy with MELAS: Clinical Presentation and Effects of Arginine Treatment

Gawne-Cain, M.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

Gebhard, B.

Participation in Neuropediatric Care

Gedik, A.

Landau-Kleffner Syndrome (Epileptic Aphasia)

Gehrlich, C.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Geigenberger, C.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Geis, T.

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Gellermann, J.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Genter, F.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Gerling, Ch.

Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review

Giagkou, E.

Use of Complementary and Alternative Medicine (CAM) in Patients with X-Linked Recessive Duchenne Muscular Dystrophy (DMD)

Gillessen-Kaesbach, G.

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

Gissen, P.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Gogoll, L.

In Delayed Myelination Count on T(o)3

Gold, R.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Goldhahn, K.

Hemispherectomy in Familial Focal Epilepsy? A Case Report of a Pharmacoresistant Epilepsy with Malformation of Cortical Development

Göpel, W.

Very Low-Birth-Weight Infants in Germany: What about Early Intervention?

Gossler, A.

In-Frame Deletion in ISPD Gene Causes Limb Girdle Muscular Dystrophy: A Case Report

Gotwald, T.

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Greulich, N.

Enterovirus Induced Opsoclonus-Myoclonus Syndrome in a 16-Month-Old Girl

Grimm, J.

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Groeschel, S.

Demyelination Load and Cerebral Atrophy in Juvenile Metachromatic Leukodystrophy

Groll, A.

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Gröschel, S.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

Groß, C. C.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Gruber-Sedlmayr, U.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Grünert, S. C.

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Grunt, S.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Haack, T.

Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report

Haack, T. B.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Haber, E.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Haberlandt, E.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Hack, T.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Hackenberg, A.

In Delayed Myelination Count on T(o)3

Severe Intellectual Disability with Speech Delay, Clumsiness, and Drug Responsive Epilepsy in a Boy with GAMT Deficiency

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Haeckl, B.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Hägele, A.

Successful Therapy of Holmes Tremor with a Silicone Hand-Wrist Orthesis and Botulinum Toxin A

Hahn, A.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Hahn, G.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Haidl, H.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Harmsen, S.

Rare Causes of Childhood Stroke: A Single-Center Experience

Hart, D.

How Useful Is General Movement Assessment and Alberta Infant Motor Scale at the Age of Three Months for Prediction of Neuromotor Outcome in an Unselected Group of High-Risk Infants?

Are 2-Year Old Children Who Underwent Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy at Risk for Behavioral Problems?

Hartlieb, T.

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Hartmann, H.

Neurocognitive Outcome in Hepatorenal Tyrosinemia

Developmental Profiles of Children with Pyridoxine-Dependent Epilepsy (PDE)

Has, C.

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Hashem, M.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Hasselmann, O.

Recommendations of How Pediatric Palliative Care Can Be Reconciled with Autonomy

Häusler, M.

Case Reports: Intracranial Abscesses

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Hedderich, J.

Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents

Sympathetic Activity of PPR-Positive Adolescents: Clinical Study

Hegen, B.

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Hehr, U.

Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Heinemeyer, J.

Meningitis Caused by Listeria Monocytogenes during Methylprednisolone Pulse Therapy

Heinen, F.

Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine

Neurological and Psychological Impairments of Children with Fetal Alcohol Spectrum Disorders: Two Case Reports

Heinrich, B.

In Delayed Myelination Count on T(o)3

Heinz-Erian, E.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Helmke, F.

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Helps, S.

How Useful Is General Movement Assessment and Alberta Infant Motor Scale at the Age of Three Months for Prediction of Neuromotor Outcome in an Unselected Group of High-Risk Infants?

Are 2-Year Old Children Who Underwent Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy at Risk for Behavioral Problems?

Hennes, E.

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Hennes, E. M.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Henzi, B.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Herberhold, T.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Herberhold, T. M.

Cochlear Edema and Sclerosis following Meningitis by S. Pneumoniae: Only Early Audiometry Allows Optimal Cochlear Implantation (CI)

Herbold, T.

Variety of Phenotypes in Chromosome 16p11.2 Deletion Syndrome

Hernáiz, Driever P.

Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin

Quantitative Sensory Testing Is Highly Sensitive in Detecting Chemotherapy-Induced Peripheral Neuropathy

Hersberger, M.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Herting, A.

Seizures after Hemispherectomy: The Role of the Insula

Herting, E.

Very Low-Birth-Weight Infants in Germany: What about Early Intervention?

Hess, K.

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Hessenauer, M.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Heussinger, N.

Paroxysmal Events in Glut1 Deficiency

Heußinger, N.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Enterovirus Induced Opsoclonus-Myoclonus Syndrome in a 16-Month-Old Girl

Heyer, C.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders

Hobbiebrunken, E.

Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement

Hoche, F.

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Hoffjan, S.

SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy

Duplication within the KCNQ2 Gene in a Child with Benign Early-Onset Epileptic Encephalopathy

Hoffmann, G.

Everolimus as Targeted mTOR Inhibition in Neonates and Infants with Tuberous Sclerosis

Hoffmann, G. F.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype

Ten Years after the International Committee of Medical Journal Editors’ Clinical Trial Registration Initiative, One Quarter of Phase 3 Pediatric Epilepsy Clinical Trials Still Remain Unpublished: A Cross-Sectional Analysis

Hofmeister, B.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Höftberger, R.

A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside

Höhn, T.

Neonatal Seizures and Response to Phenobarbitone: A Three-Year Single-Center Experience

Holinski-Feder, E.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Holthausen, H.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

Hooijmans, M.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Hoppen, T.

Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler

Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation

Horn, A.

Rare Causes of Childhood Stroke: A Single-Center Experience

Hornig, S.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Hörning, A.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Horsthemke, B.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Hörtnagel, K.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Horvath, R.

Childhood Mitochondrial Diseases: Diagnosis and Potential Therapies

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Hoyer, P. F.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Superiority of Renal MRI to Ultrasound in Children with Tuberous Sclerosis Complex (TSC): Detecting of Renal Angiomyolipomas (AML) with Elevated Risk of Bleeding

Hu, H.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Hubmann, H.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Hübner, A.

Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement

Huebner, A.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Huebner, C.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Hulkova, H.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Hummel, H.

Fingolimod in Highly Active Pediatric Multiple Sclerosis

Hummel, H.-M.

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Hüning, B.

Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension

Huppke, P.

Acute Severe Combined Demyelination: Case Report

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Fingolimod in Highly Active Pediatric Multiple Sclerosis

Husain, R. A.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Isbrand, D.

The Voltage-Gated Sodium Channel Nav1.2 Contributes to Neurodegeneration in an Animal Model of Multiple Sclerosis

Isermann, J.

Use of an Electronic Version of the ICF-CY in a Rehabilitation Clinic

Ismail, M.

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Ivanov, I.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Jacoby, D.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Jaggy, L.

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Jakob, A.

A Case of Breath Holding Spells Resulting in Pacemaker Implantation

Janisch, M.

What Kind of General and Special Palliative Care Do Children, Adolescents, and Young Adults with Duchenne Muscular Dystrophy Need?

Jansen, C.

Muscle-Adaptation in Children with Acquired Brain Injuries

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Jansen, K.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Joset, P.

Severe Intellectual Disability with Speech Delay, Clumsiness, and Drug Responsive Epilepsy in a Boy with GAMT Deficiency

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Josset, P.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Joy, H. M.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

Juenger, H.

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Jung, S.

Age-Specific Changes of the AMPA Receptor and ADAR Enzyme Expression Profile in the Neonatal Mouse Brain due to Pilocarpine-Induced Seizures

Jünger, H.

Longitudinal Extensive Transverse Myelitis following T-ALL

Kaernbach, C.

Sympathetic Activity of PPR-Positive Adolescents: Clinical Study

Kaindl, A. M.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Kaindl, AM

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Kaiser, A.-S.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

Kaiser, D.

Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Kaiser, O.

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Superiority of Renal MRI to Ultrasound in Children with Tuberous Sclerosis Complex (TSC): Detecting of Renal Angiomyolipomas (AML) with Elevated Risk of Bleeding

Kalbhenn, T.

Seizures after Hemispherectomy: The Role of the Insula

Kalina, T.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Kaller, C. P.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Kan, H.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Karenfort, M.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Rare Causes of Childhood Stroke: A Single-Center Experience

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Kathemann, S.

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Kauffmann, B.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Kehrer, C.

Demyelination Load and Cerebral Atrophy in Juvenile Metachromatic Leukodystrophy

Keyvani, K.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Kienle, N.

Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2

Kieslich, M.

Inherited Mitochondrial Neuropathy: Differential Diagnosis of Pediatric Axonal Neuropathy

X-Linked Periventricular Heterotopia: Differential Diagnosis of Female Patients

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Kiess, W.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Kirkham, F. J.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

Kirschner, J.

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

A Case of Breath Holding Spells Resulting in Pacemaker Implantation

Kizina, K.

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Klee, D.

Rare Causes of Childhood Stroke: A Single-Center Experience

Klein, A.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Klein, C.

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

Kleinle, S.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Kleiter, I.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Klemann, C.

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Klepper, J.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Enterovirus Induced Opsoclonus-Myoclonus Syndrome in a 16-Month-Old Girl

Paroxysmal Events in Glut1 Deficiency

Klinge, L.

In-Frame Deletion in ISPD Gene Causes Limb Girdle Muscular Dystrophy: A Case Report

Klotz, K. A.

A Case of Breath Holding Spells Resulting in Pacemaker Implantation

Kluger, G.

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Study Group: Personalized Therapy in Rare Pediatric Epilepsies

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Koch, M.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Koehler, U.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Kohl, B.

Rare Case of Miller-Fisher Syndrome

Kohler, B.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Köhler, C.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Unclear Encephalopathy: Accurate Environmental History Conclusive!

SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy

Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration

Duplication within the KCNQ2 Gene in a Child with Benign Early-Onset Epileptic Encephalopathy

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Kohlschütter, A.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Kölbel, H.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Kölbel, Heike

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

König, N.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Konrad, K.

Rhabdomyolysis as a Rare Complication of Diabetic Ketoacidosis in a Twelve-Year-Old Boy

Kopp, U. A.

Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents

Korenke, C.

Seizures after Hemispherectomy: The Role of the Insula

Korenke, G. C.

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Neonatal Moyamoya Disease of Unclear Origin

Korinthenberg, R.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Rare Case of Miller-Fisher Syndrome

A Case of Breath Holding Spells Resulting in Pacemaker Implantation

Kornek, B.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Kortschak, A.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Kössler, M.

Landau-Kleffner Syndrome (Epileptic Aphasia)

Kößler, M.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Koustenis, E.

Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin

Kowald, T.

Neonatal Moyamoya Disease of Unclear Origin

Kraemer, N.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Krägeloh-Mann, I.

Demyelination Load and Cerebral Atrophy in Juvenile Metachromatic Leukodystrophy

Kraus, V.

Longitudinal Extensive Transverse Myelitis following T-ALL

Kreß, W.

In-Frame Deletion in ISPD Gene Causes Limb Girdle Muscular Dystrophy: A Case Report

Krieg, S. M.

Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine

Kroger, H.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Krüger, M.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures

Kruker, A. T.

Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Krumm, A.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Kudernatsch, M.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Kunze, A.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Kunze, S.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Künzle, C.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Küpper, H.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

Kurlemann, G.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Küster, S.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Kutschke, G.

Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy

Kutzbach, T.

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Lampert, A.

Ten Years after the International Committee of Medical Journal Editors’ Clinical Trial Registration Initiative, One Quarter of Phase 3 Pediatric Epilepsy Clinical Trials Still Remain Unpublished: A Cross-Sectional Analysis

Landgraf, M. N.

Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine

Neurological and Psychological Impairments of Children with Fetal Alcohol Spectrum Disorders: Two Case Reports

Lange, J.

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Langen, H.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Lasch, P.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Latal, B.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

Lechner, C.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Leiendecker, B.

Paroxysmal Events in Glut1 Deficiency

Leiz, S.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Lemke, J.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Lezius, S.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Lieber, S.

Quantitative Sensory Testing Is Highly Sensitive in Detecting Chemotherapy-Induced Peripheral Neuropathy

Liehr, T.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Lindmayer, F.

Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy

Lipp, J.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Lischetzki, G.

Meningitis Caused by Listeria Monocytogenes during Methylprednisolone Pulse Therapy

Lobitz, S.

Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin

Lochmüller, H.

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?

Overview and Update of Congenital Myasthenic Syndromes

Lorenzen, A.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Lorey, M.

Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler

Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation

Losch, H.

Neonatal Moyamoya Disease of Unclear Origin

Lowes, L.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Lücke, T.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Influence of Maternal Graduation on the Cognitive Development of Very Low-Birth-Weight Infants

Unclear Encephalopathy: Accurate Environmental History Conclusive!

α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders

SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy

Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration

Preterm and Full-Term Children Do Not Differ in Their Perspective-Taking Ability

Duplication within the KCNQ2 Gene in a Child with Benign Early-Onset Epileptic Encephalopathy

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Lühl, S.

Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6

Lukas, C.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Luo, X.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Lüsebrink, N.

Inherited Mitochondrial Neuropathy: Differential Diagnosis of Pediatric Axonal Neuropathy

Lutz, S.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Superiority of Renal MRI to Ultrasound in Children with Tuberous Sclerosis Complex (TSC): Detecting of Renal Angiomyolipomas (AML) with Elevated Risk of Bleeding

Maier, O.

Performing Evoked Potentials in Pediatrics: Methodology, Clinical Indications, and Limits

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Majer, F.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Makowski, C.

Longitudinal Extensive Transverse Myelitis following T-ALL

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Mall, V.

Longitudinal Extensive Transverse Myelitis following T-ALL

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Marquard, K.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2

Marquardt, T.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Marschik, P. B.

It Is Not Too Early: Clinical Implications of Early Spontaneous Movements

Mathis, D.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Matzker, E.

Acute Severe Combined Demyelination: Case Report

Mayatepek, E.

Rare Causes of Childhood Stroke: A Single-Center Experience

Mayer, V.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Mayr, H.

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Mayr, J.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Mazzone, L.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

McDonald, C. M.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Meier, O.

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Meier, U.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Melliger, A.

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Mengel, E.

α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders

Mentzel, H. J.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Mercuri, E.

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Methling, B.

α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders

Metternich, B.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Meuli, M.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

Meuth, S. G.

Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis

Meyer, U.

Neurocognitive Outcome in Hepatorenal Tyrosinemia

Michel, J.

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Mignot, C.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Milian, M.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Moehrlen, U.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

Moein, G.

X-Linked Periventricular Heterotopia: Differential Diagnosis of Female Patients

Moiseeva, S.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Möller, K.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Möller-Hartmann, C.

Tuberculosis Meningitis with Brainstem Mass Lesion—Adjunctive Treatment with Thalidomide: A Case Report

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Moser, K.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Mreyen, S.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Mückschel, M.

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Müller, C. R.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Münchau, A.

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

Muntoni, F.

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Musante, L.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Nastulla, T.

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Neininger, M. P.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Nestler, M.

Hypocalcemic Partial Seizures in the Newborn

Neu, A.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Neubauer, B. A.

New Findings in Genetic Focal Epilepsies: The GATOR1 Complex as a Hub for Idiopathic/Genetic and Structural Focal Epilepsies

Neuen-Jacob, E.

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Neuhann, T.

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Neuloh, G.

Case Reports: Intracranial Abscesses

Neumann, H.

Preterm and Full-Term Children Do Not Differ in Their Perspective-Taking Ability

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Nickel, M.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Nickel, P.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Nicolai, H.

Unclear Encephalopathy: Accurate Environmental History Conclusive!

Niebuhr, U.

Use of an Electronic Version of the ICF-CY in a Rehabilitation Clinic

Niedermeyer, H. P.

Cochlear Edema and Sclerosis following Meningitis by S. Pneumoniae: Only Early Audiometry Allows Optimal Cochlear Implantation (CI)

Niks, E.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Nissen, A.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Nobis, K.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Nolte-Buchholtz, S.

What Kind of General and Special Palliative Care Do Children, Adolescents, and Young Adults with Duchenne Muscular Dystrophy Need?

Aspects of Palliative Care in Child Neurology

Noßwitz, U.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Noti, F.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Nuoffer, J-M.

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Nüßlein, T.

Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler

Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation

Ohlenbusch, A.

A New Mitochondrial tRNA(Met)—Gene Mutation in a 12-Year-Old Boy with MELAS: Clinical Presentation and Effects of Arginine Treatment

Olze, A.

Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus

Omran, H.

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Ong, T.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Opitz, D.

Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy

Opladen, T.

New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype

Orlikowsky, Th.

Case Reports: Intracranial Abscesses

Pallivathukal, S.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Panzer, A.

CDKL 5 Mutation: The Viewpoint of Self-Help Organization

Hypocalcemic Partial Seizures in the Newborn

Hemispherectomy in Familial Focal Epilepsy? A Case Report of a Pharmacoresistant Epilepsy with Malformation of Cortical Development

Papuc, M.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Park, S.-M.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Pauschek, J.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Pechmann, A.

Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures

Peltz, S. W.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Perret-Hoigné, E.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Peterli, J.

Performing Evoked Potentials in Pediatrics: Methodology, Clinical Indications, and Limits

Petermann, F.

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Petrova, S.

Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts

Pfahl, S.

Neonatal Seizures and Response to Phenobarbitone: A Three-Year Single-Center Experience

Pfammatter, J. P.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Pfeifer, N.

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Philippi, H.

Participation in Neuropediatric Care

Picker-Minh, S.

Phenotype Variability of Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease IMNEPD

Pieper, T.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Pietz, J.

Family-Oriented Palliative Care: Parents’ Perspective and Experience

Plecko, B.

In Delayed Myelination Count on T(o)3

Severe Intellectual Disability with Speech Delay, Clumsiness, and Drug Responsive Epilepsy in a Boy with GAMT Deficiency

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Update in Metabolic Epilepsies

Pöhlau, D.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Poloni, C.

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Polster, T.

Hemispherectomy in Familial Focal Epilepsy? A Case Report of a Pharmacoresistant Epilepsy with Malformation of Cortical Development

Seizures after Hemispherectomy: The Role of the Insula

Porto, L.

Inherited Mitochondrial Neuropathy: Differential Diagnosis of Pediatric Axonal Neuropathy

X-Linked Periventricular Heterotopia: Differential Diagnosis of Female Patients

Povysil, B.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Preuße, C.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Pringsheim, M.

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Prokisch, H.

Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?

Paroxysmal Dyskinesia in ECHS1 Defect with Globus Pallidus Lesions

Pross, I.

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Prott, E.

Variety of Phenotypes in Chromosome 16p11.2 Deletion Syndrome

Prüfe, J.

Neurocognitive Outcome in Hepatorenal Tyrosinemia

Developmental Profiles of Children with Pyridoxine-Dependent Epilepsy (PDE)

Püst, B.

Rare Case of Miller-Fisher Syndrome

Rating, T.

Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy

Rauch, A.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Reich, L.

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Reihle, C.

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Reindl, M.

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Reindl, T.

Quantitative Sensory Testing Is Highly Sensitive in Detecting Chemotherapy-Induced Peripheral Neuropathy

Rethmann, C.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

Reutermann, J. E.

Sympathetic Activity of PPR-Positive Adolescents: Clinical Study

Reutlinger, C.

Use of an Electronic Version of the ICF-CY in a Rehabilitation Clinic

Riebling, P.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Riedel, J.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Ries, M.

Ten Years after the International Committee of Medical Journal Editors’ Clinical Trial Registration Initiative, One Quarter of Phase 3 Pediatric Epilepsy Clinical Trials Still Remain Unpublished: A Cross-Sectional Analysis

Rödl, T.

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Romeike, B.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Rona, S.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Ropers, H. H.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Rössig, C.

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Rossler, L.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Rost, S.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Rostasy, K.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Rostásy, K.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Rückert, J. C.

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Rueckriegel, S. M.

Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin

Ruf, S.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Sabir, H.

Neonatal Seizures and Response to Phenobarbitone: A Three-Year Single-Center Experience

Sacco, E.

Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Salamano, E.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Sandrieser, T.

Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler

Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation

Sass, O.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Scarpa, M.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Schallner, J.

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

Schänzer, A.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Schara, U.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Use of Complementary and Alternative Medicine (CAM) in Patients with X-Linked Recessive Duchenne Muscular Dystrophy (DMD)

Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?

Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody Positive Juvenile Myasthenia Gravis

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Superiority of Renal MRI to Ultrasound in Children with Tuberous Sclerosis Complex (TSC): Detecting of Renal Angiomyolipomas (AML) with Elevated Risk of Bleeding

Schattling, B.

The Voltage-Gated Sodium Channel Nav1.2 Contributes to Neurodegeneration in an Animal Model of Multiple Sclerosis

Schaudeck, M.

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Schauer, U.

Influence of Maternal Graduation on the Cognitive Development of Very Low-Birth-Weight Infants

Scheffner, T.

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Schell, C.

Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome

Schilling, S.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Schimmel, M.

Pediatric Multiple Sclerosis Is Associated with Brain Growth Failure

Role of MOG Antibodies in the Differential Diagnosis of Acquired Demyelinating CNS Syndromes in Children

Schindler, K.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Schipper, S.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Schirmer, S.

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Schlump, J-U.

Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review

Schlüter, G.

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Schmitt, B.

Severe Intellectual Disability with Speech Delay, Clumsiness, and Drug Responsive Epilepsy in a Boy with GAMT Deficiency

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Schmitt, K.

Neuroimaging in Childhood Headaches and Psychiatric Disorders: Results of a Prospective Study

Schmitt-Mechelke, T.

Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Schneider, R.

Case Reports: Intracranial Abscesses

Schoberer, A.

Case Reports: Intracranial Abscesses

Schoberer, M.

Case Reports: Intracranial Abscesses

Schorling, D.

Early Lethal Neurodegeneration with Myasthenic and Myopathic Features: A New Genetic Syndrome Due to Previously Undescribed ALG14 Mutations

Schreglmann, M.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

How Useful Is General Movement Assessment and Alberta Infant Motor Scale at the Age of Three Months for Prediction of Neuromotor Outcome in an Unselected Group of High-Risk Infants?

Are 2-Year Old Children Who Underwent Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy at Risk for Behavioral Problems?

Schroeder, A. S.

Muscle-Adaptation in Children with Acquired Brain Injuries

Schröter, A.

Unclear Encephalopathy: Accurate Environmental History Conclusive!

Schroth, M.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Schubert-Bast, S.

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Schuhfried, O.

A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside

Schuler, E.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype

Schuler, Elisabeth

Development and Evaluation of a Computer-Controlled System to Assess Associative Visual Learning and Memory in Zebrafish Larvae

Schulz, A.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Schulze-Bonhage, A.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Schwartz, O.

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Schweiger, T.

Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review

Schwerin-Nagel, A.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Schwindt, W.

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Seidel, A.

Participation in Neuropediatric Care

Seidl, R.

A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside

Selzer, L.

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Senderek, J.

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Shin, Y.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Sikora, J.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Simmons, L.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Simonati, A.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Smitka, M.

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Sollmann, N.

Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine

Sorantin, E.

Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome

Spaich, C.

Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2

Specchio, N.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Speitel, K.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Spiegel, R.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Results of North Star Ambulatory Assessments in the Phase 3 Ataluren Confirmatory Trial in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (ACT DMD)

Spiegler, J.

Very Low-Birth-Weight Infants in Germany: What about Early Intervention?

Spönemann, N.

Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy

Stange, M.

Neurocognitive Outcome in Hepatorenal Tyrosinemia

Stark, W.

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Fingolimod in Highly Active Pediatric Multiple Sclerosis

Staudt, M.

Cochlear Edema and Sclerosis following Meningitis by S. Pneumoniae: Only Early Audiometry Allows Optimal Cochlear Implantation (CI)

Mirror Movements In Unilateral Spastic Cerebral Palsy: Effects Of A Goal-Oriented Bimanual Therapy

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Dopamine-Responsive Dystonia: An Important Differential Diagnosis to Cerebral Palsy

Stehling, F.

Tuberculosis Meningitis with Brainstem Mass Lesion—Adjunctive Treatment with Thalidomide: A Case Report

Steindl, K.

In Delayed Myelination Count on T(o)3

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Steinert, M.

Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration

Steinlin, M.

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Thrombolysis and Thrombectomy in Children with Acute Ischemic Stroke

Stelzner, A.

CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes

Stenzel, W.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Stephani, U.

Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents

Sympathetic Activity of PPR-Positive Adolescents: Clinical Study

Stettner, G. M.

Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement

Stiller, B.

A Case of Breath Holding Spells Resulting in Pacemaker Implantation

Stöhr, K.

Cochlear Edema and Sclerosis following Meningitis by S. Pneumoniae: Only Early Audiometry Allows Optimal Cochlear Implantation (CI)

Storch, K.

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Straßer, K.

Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report

Sträter, R.

Attention after Thrombectomy in Pediatric Stroke: Keep in Mind the Possibility of a Progressive Stenosing Cerebral Vasculopathy

Straub, V.

The Role of Magnetic Resonance Imaging in the Diagnosis and Assessment of Children with Genetic Muscle Disease

Strölin, M.

Demyelination Load and Cerebral Atrophy in Juvenile Metachromatic Leukodystrophy

Strotmann, P.

Longitudinal Extensive Transverse Myelitis following T-ALL

Longitudinal Extensive Transverse Myelitis following T-ALL

Strozzi, S.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Sweeney, H. L.

The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies

Syrbe, S.

How Do Children and Adolescents Experience Their Seizures? A Survey on Disease Concepts, Knowledge, and Coping

Taylor, A. F. M.

Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia

Teig, N.

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

Influence of Maternal Graduation on the Cognitive Development of Very Low-Birth-Weight Infants

Thiels, C.

α-Fucosidase Deficiency: A Rare Differential Diagnosis of the Eye-of-the-Tiger Sign and Extrapyramidal Movement Disorders

Thiels, Ch.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome

SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy

Cockayne Syndrome: Two Siblings with Neurodegenerative Disease and Infection-Associated Deterioration

Duplication within the KCNQ2 Gene in a Child with Benign Early-Onset Epileptic Encephalopathy

Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study

Thorpe, Bione S.

CDKL 5 Mutation: The Viewpoint of Self-Help Organization

Tibussek, D.

Rare Causes of Childhood Stroke: A Single-Center Experience

Neonatal Seizures and Response to Phenobarbitone: A Three-Year Single-Center Experience

Topaloglu, H.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Tournier, D.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

Traupe, O.

Sympathetic Activity of PPR-Positive Adolescents: Clinical Study

Trauzettel-Klosinski, S.

Radiological Findings in Children and Adolescents with Homonymous Visual Field Defects: Types of Lesion and Frequency

Travan, L.

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Trepels-Kottek, S.

Case Reports: Intracranial Abscesses

Trepte-Freisleder, F.

Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine

Trollmann, R.

Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report

Age-Specific Changes of the AMPA Receptor and ADAR Enzyme Expression Profile in the Neonatal Mouse Brain due to Pilocarpine-Induced Seizures

Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy

Tulinius, M.

Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Ungerath, K.

Meningitis Caused by Listeria Monocytogenes during Methylprednisolone Pulse Therapy

Urbach, H.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Utz, N.

Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review

Valente, André

Development and Evaluation of a Computer-Controlled System to Assess Associative Visual Learning and Memory in Zebrafish Larvae

van Karnebeek, C.

Developmental Profiles of Children with Pyridoxine-Dependent Epilepsy (PDE)

van Kuilenburg, A. BP.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

van Moers, A.

Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients

Verma, R.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Verschuuren, J.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Viemann, M.

Neonatal Moyamoya Disease of Unclear Origin

Vlaskova, H.

Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene

Vogelsang, C.

Everolimus as Targeted mTOR Inhibition in Neonates and Infants with Tuberous Sclerosis

Vogl, M.

Tuberculosis Meningitis with Brainstem Mass Lesion—Adjunctive Treatment with Thalidomide: A Case Report

Vollmer, B.

Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy

How Useful Is General Movement Assessment and Alberta Infant Motor Scale at the Age of Three Months for Prediction of Neuromotor Outcome in an Unselected Group of High-Risk Infants?

Are 2-Year Old Children Who Underwent Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy at Risk for Behavioral Problems?

von der Hagen, M.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

What Kind of General and Special Palliative Care Do Children, Adolescents, and Young Adults with Duchenne Muscular Dystrophy Need?

Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Aspects of Palliative Care in Child Neurology

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

von der Heiden, K.

Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region

von Kalle, T.

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

von Moers, A.

Hypocalcemic Partial Seizures in the Newborn

Hemispherectomy in Familial Focal Epilepsy? A Case Report of a Pharmacoresistant Epilepsy with Malformation of Cortical Development

von Stülpnagel-Steinbeis, C.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Study Group: Personalized Therapy in Rare Pediatric Epilepsies

Vulcu, S.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Wachowsky, M.

Ehlers-Danlos Syndrome, Kyphoscoliotic Type (Formerly Type VI) as Differential Diagnosis to Neuromuscular Diseases

Wagner, B.

Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition

Wagner, K.

Hippocampus Sparing Resections within the Temporal Lobe in Adolescents with Epilepsy: Impact on Cognition and Remaining Hippocampal Volume

Walter, M.

Massive Parallel Sequencing with a Multigene Panel (MGPS): Experiences with α-Dystroglycanopathies

Walter, M. C.

Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy

Congenital Myasthenic Syndromes: Efficiency and Pitfalls of Phenotype-Based Gene Panel Testing

Wapp, M.

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Wawer, A.

Longitudinal Extensive Transverse Myelitis following T-ALL

Webb, A.

Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle

Weber, P.

Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes

Wedegärtner, S.

Superiority of Renal MRI to Ultrasound in Children with Tuberous Sclerosis Complex (TSC): Detecting of Renal Angiomyolipomas (AML) with Elevated Risk of Bleeding

Wegner, S.

Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents

Weise, S.

Successful Therapy of Holmes Tremor with a Silicone Hand-Wrist Orthesis and Botulinum Toxin A

Trichotillomania under a Therapy with Lisdexamfetamine

Weishaupt, E.

Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension

Weiss, J.

Nesprinopathies: Diagnostic Challenge in a Wide Clinical Range of Phenotypes

Weissbrich, B.

Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases

Weisstanner, C.

Childhood Arterial Ischemic Stroke: The Influence of Lesion Location on Outcome

Weitkämper, A.

Influence of Maternal Graduation on the Cognitive Development of Very Low-Birth-Weight Infants

Preterm and Full-Term Children Do Not Differ in Their Perspective-Taking Ability

Wellmann, S.

Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures

Wernicke, C. M.

Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children

Westenberger, A.

Novel Adenylate Cyclase 5 Gene (ADCY5) Mutations Cause a New Phenotype of Alternating Hemiplegia of Childhood (AHC), Expanding the Clinical Spectrum of ADCY5-Related Hyperkinetic Dyskinesias

Wibbeler, E.

Long-Term Follow-Up of Patients with Congenital Myasthenic Syndromes: What Do We Learn?

Wieczorek, D.

Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15

Wienker, T. F.

Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity

Wildbolz, M.

Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy

Wilichowski, E.

Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement

In-Frame Deletion in ISPD Gene Causes Limb Girdle Muscular Dystrophy: A Case Report

A New Mitochondrial tRNA(Met)—Gene Mutation in a 12-Year-Old Boy with MELAS: Clinical Presentation and Effects of Arginine Treatment

Wilke, M.

Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia

Wilken, B.

Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome

Wille, D. A.

Preliminary Results in Children with Myelomeningocele after Fetal Surgery: Data from the Zurich Cohort

Williams, R.

Intracerebroventricular Cerliponase Alfa (BMN 190) in Children with CLN2 Disease: Interim Results from a Phase 1/2, Open-Label, Dose-Escalation Study

Wimmer, C.

Muscle-Adaptation in Children with Acquired Brain Injuries

Winkler, P.

Prediction of Contralateral Hand Function after Hemispherectomy for Refractory Epilepsies: Experience from 102 Pediatric Cases

How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data

Wirth-Barben, G.

West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy

Witt, S.

Preterm and Full-Term Children Do Not Differ in Their Perspective-Taking Ability

Wittes, J.

Natural History of CLN2 Disease: Quantitative Assessment of Disease Characteristics and Rate of Progression

Woermann, F. G.

Seizures after Hemispherectomy: The Role of the Insula

Wohlrab, G.

A Combined Metabolic–Genetic Approach to Early-Onset Epileptic Encephalopathies: Results from a Swiss Study Cohort

Wolf, C.

Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy

Wolff, M.

SCN2A A Sequence Variant in Mosaic State in a Patient with Infantile Epileptic Encephalopathy

In Vitro Characterization of KCNT1 Mutations from Pediatric Patients

Wörle, H.

Cluster Headache in Childhood and Adolescence: Two Case Reports

Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports

Wruk, M.

Botulinum Toxin in Paediatric Neuro-Rehabilitation

Würfel, J.

Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients

Zeiner, F.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Zellner, H.

Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015

Landau-Kleffner Syndrome (Epileptic Aphasia)

Zieger, B.

Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene

Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures

Ziegler, A.

Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua

New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype

Everolimus as Targeted mTOR Inhibition in Neonates and Infants with Tuberous Sclerosis

Ziegler, A. E.

Experiences in the Implication of Palliative Care Counseling and Attendance at a German Neuropediatric Ward

Zimmer, K. P.

Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)

Zmyj, N.

Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension

Preterm and Full-Term Children Do Not Differ in Their Perspective-Taking Ability

Zotter, S.

Landau-Kleffner Syndrome (Epileptic Aphasia)

Zschocke, A.

Landau-Kleffner Syndrome (Epileptic Aphasia)

Zuzak, T.

Use of Complementary and Alternative Medicine (CAM) in Patients with X-Linked Recessive Duchenne Muscular Dystrophy (DMD)