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Badura, Katharina
FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 396. Childhood Hemorrhagic Stroke—A 7-Year Single-Center Experience
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
P 1152. Assessment of Therapeutically Guided Serious Gaming from the Point of View of the Treated Children and Adolescents—A Pilot Study
Balci, Meral
P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids
Balg, Stefanie
P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?
Balmer, Christian
FV 571. Cardiac Kids with Stroke
Baltsavias, Gerasimos
FV 820. Pediatric Moyamoya Angiopathy: A Rapid Progressive Disease in Children < 5 Years of Age
Bamborschke, Daniel
P 1001. A Pathogenic GABRB3 Variant Is Associated with Cleft Palate in a Patient with Epileptic Encephalopathy
Bast, Thomas
FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies
Bauer, Angela
FV 776. sEMG Biofeedback Therapy in Children with Cerebral Palsy
Baumann, Matthias
P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents
Baumgartner, Matthias R.
FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
Baumkötter, Jochen
P 1111. Case Report of a Juvenile Patient with Niemann–Pick’s Disease Type C
Bayram, Dilan
P 882. Four-Level Release (Rideau) and Glucocorticoid Therapy in Patients with DMD—Additive Positive Effect on Ambulation
Beblo, Skadi
FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
Becker, Kerstin
FV 747. Early-Onset Progressive Dystonia in Childhood with New Mutations in KMT2B
P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?
Becker, Lena-Luise
P 306. Role of Cdk5rap2 in Neocortical Development
Beck-Wödl, Stefanie
FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders
P 1155. Focal Epilepsy Difficult to Treat in Hermann–Pallister’s Syndrome (KBG Syndrome)
Beghetti, Maurice
FV 571. Cardiac Kids with Stroke
Begtrup, Amber
FV 241. Mutations in NFE2L2 Lead to a Novel Treatable Neurological Disorder with Leukoencephalopathy
Behnecke, Anne
P 956. Next-Generation Sequencing in Patient Care—Arrived or Rejected in Rare Diseases?
Bernert, Günther
P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries
Bernhard, Matthias K.
FV 918. How Do Pediatricians and General Practitioners Deal with Epilepsy Patients? Results of a Structured Interview
Berry, Katherine
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones
Bertsche, Astrid
FV 918. How Do Pediatricians and General Practitioners Deal with Epilepsy Patients? Results of a Structured Interview
FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?
P 1011. Think Unusual—Developmental Delay Plus: Multimodal Diagnosis of Menkes’ Syndrome
Bertsche, Thilo
FV 918. How Do Pediatricians and General Practitioners Deal with Epilepsy Patients? Results of a Structured Interview
Berweck, Steffen
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis
P 1152. Assessment of Therapeutically Guided Serious Gaming from the Point of View of the Treated Children and Adolescents—A Pilot Study
Beschle, Judith
FV 948. Diffusion Tensor Imaging Parameters in Metachromatic Leukodystrophy: Biomarkers for Disease Progress and Therapeutically Therapeutic Evaluation
Bettendorf, Markus
P 780. Misdiagnosis of Child Abuse—Fibrodysplasia Ossificans Progressiva as a Therapy-Relevant Differential Diagnosis in Infancy
Betzler, Cornelia
P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis
Beyerlein, Andreas
FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies
Bhathal, Hari
IP 112. Cannabidiol Treatment Effect and Adverse Events in Patients with Lennox–Gastaut’s syndrome: Pooled Results from Two Trials
Bien, Christian G.
P 556. Ketogenic Dietary Therapies—Retrospective Assessment of 143 Children Treated at the Bethel Epilepsy Center from 2003 to 2016
Bigi, Sandra
FV 513. A Potential Risk of Inadequate Prognosis in Hypothermic Children after Asphyxia with Delayed Abnormalities in Diffusion-Weighted Images
Biskup, Saskia
P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy
P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings
Blakely, Emma
FV 697. Biallelic Mutations in SCYL1 Cause CALFAN-Syndrome (Cholestasis, Acute Liver Failure, and Neurodegeneration), A Congenital Disorder of Intracellular Trafficking with a Variable Neurological Phenotype
Blankenburg, Markus
P 1139. Gradenigo’s Syndrome: Two New Case Studies
Blaschek, Astrid
FV 318. Infant Automated Motion Recognition Technology Using RGB-Depth Sensors for Markerless, Rater-Independent Detection of Abnormal Movements in Early Infancy—In a Motion Project
FV 658. Cognitive Impairment, Depression, Fatigue, and Quality of Life in Pediatric-Onset Multiple Sclerosis: Results of the Multiple Sclerosis Inventory of Cognition in ADOlescents Study
P 913. Heterozygous Nonsense Variant in the TCF20 Gene as a Cause of Congenital Myopathy
Bluemchen, Katharina
P 1092. The Challenging Nature of Cerebral TBC Manifestations in Children and Young Adults
Bodensteiner, Christoph
FV 318. Infant Automated Motion Recognition Technology Using RGB-Depth Sensors for Markerless, Rater-Independent Detection of Abnormal Movements in Early Infancy—In a Motion Project
Boie, G.
FV 1091. C1-esterase Inhibitor Treatment Prevents Blood–Brain Barrier Dysfunction in the Neonatal Mouse Brain after Acute Systemic Hypoxia
Boltshauser, Eugen
P 295. Everolimus Trial for a Patient with Bannayan–Riley–Ruvalcaba’s Syndrome and Progressive Lipomatosis
Bonfert, Michaela Veronika
FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 396. Childhood Hemorrhagic Stroke—A 7-Year Single-Center Experience
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017
Bonnen, Penelope
FV 697. Biallelic Mutations in SCYL1 Cause CALFAN-Syndrome (Cholestasis, Acute Liver Failure, and Neurodegeneration), A Congenital Disorder of Intracellular Trafficking with a Variable Neurological Phenotype
Borell, Sabine
FV 880. Disorders of Coagulation in Duchenne Muscular Dystrophy?—Results of a Registry-Based Online Questionnaire
Borggräfe, Ingo
FV 510. Influence of Anticonvulsive Treatment on the EEG and the Neuropsychological Features in Children with Rolandic Epilepsy
FV 257. Munich Early Recognition of Childhood Stroke—More than a FAST Screening Tool
FV 561. Childhood Stroke: Awareness, Interest and Knowledge among the Pediatric Community
FV 394. Childhood Arterial Ischaemic Stroke—Results of a German Nationwide Surveillance Study 2015 to 2017
Bornheimer, Annalena
FV 449. Cerebral Blood Flow Volume and Gray Matter Volume across a Wide Age Range
Bösing, Hendrik
P 973. Case Report of a 13-Year-Old Boy with Multiple Sclerosis and Obesity Caused by a MC4-Receptor Mutation
Boy, Nikolas
FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
Brämswig, Nuria
P 308. Autosomal Recessive Mutations in the NALCN Gene: A Rare Cause of a Severe Developmental Disorder with Facial Dysmorphia, Epilepsy and Cheyne–Stokes/Biot’s Respiration with Central Apneas
Brand, Joerg
P 1103. Fatal Outcome of Metapneumovirus Infection in Patient with 4H Syndrome
Brandl, Ulrich
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Brenner, Sebastian
P 916. Lissencephaly and Prolonged Survival of a Male Infant with MICPCH and a Noval Mutation in the CASK Gene, Xp11.4
Brentrup, Angela
FV 1177. Genetic Causes of Congenital Hydrocephalus
Breu, Markus
FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
Breuer, Anna Sophie
P 379. Objective Assessment of Central Nervous Odor Processing in Infancy
Brockmann, Knut
FV 1119. Incidence of Epilepsies and Epileptic Syndromes in Children and Adolescents: A Prospective Study in Göttingen, Germany in 2014
FV 1118. The Acquisition of Rare Neurological Disorders in Childhood (“ESNEK”)—Interim Results after 4 Years
Broser, Philip
P 1166. Isolated Oculomotor Nerve Palsy as Primary Manifestation of Guillain–Barré’s Syndrome—A Case Report with Focus on Clinical and Electrophysiological Features
Broser, Philip Julian
FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children
FV 113. Electrophysiological Diagnostic of Neuromuscular Diseases in Newborns, Infants, and Toddlers
Brösse, Ines
P 694. TRIP12 Variants as a Cause of Mental Disability with or without Autism
Brotschi, Barbara
FV 571. Cardiac Kids with Stroke
Brunner-Kainz, Michaela
P 1030. MRI Pattern in Neurodegeneration with Brain Iron Accumulation and Fucosidosis Appear Similar
Buchert, Rebecca
FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders
Buchert-Lo, Rebecca
P 968. Vitamine B6-Dependent Epilepsy in a 14-Year-Old Girl with Drug-Resistant Seizures and Recurring Status Epilepticus
Buelow, Markus
P 328. Novel Homozygous Variants Confirm SPTBN4-Related Congenital Myopathy and Expand the Clinical Phenotype
Buerki, Sarah
FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children
Burdach, Stefan
P 1079. Early Diagnosis of Neuromyelitis Optica Spectrum Disease as a Prerequisite for Optimal Therapy Management—Report of a Case
Burghes, Arthur H. M.
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones