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Lagae, Lieven
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Landgraf, Mirjam N.
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
Langer, Claudia
P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy
Langer, Thorsten
FV 880. Disorders of Coagulation in Duchenne Muscular Dystrophy?—Results of a Registry-Based Online Questionnaire
FV 953. Parents’ Experiences during the Compassionate Use Program (Nusinersen) for Patients with Spinal Muscular Atrophy Type 1—A Qualitative Interview Study
P 900. Decision Making Regarding Ventilator Support in Children with SMA type 1—A Cross-sectional Survey among German Physicians
Latal, Bea
P 233. Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative Disorder
Laugwitz, Lucia
FV 943. Facilitating a Molecular Diagnosis as Soon as Possible: Diagnostic Exome in Neurometabolic Disorders
Laux, Linda
IP 110. Maintenance of Long-Term Safety and Efficacy of Cannabidiol Treatment in Dravet’s Syndrome: Results of an Open-Label Extension Trial (GWPCARE5)
Lebek, Susanne
P 882. Four-Level Release (Rideau) and Glucocorticoid Therapy in Patients with DMD—Additive Positive Effect on Ambulation
Lechner, Christian
P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents
Lehbrink, Ruth
P 1011. Think Unusual—Developmental Delay Plus: Multimodal Diagnosis of Menkes’ Syndrome
Leiendecker, Bärbel
FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
Leis, Thomas
P 1081. PTEN-Associated Macrocephaly in a 3-Year-Old Girl
Leiz, Steffen
P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids
Lekaditi, Dimitra
FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children
FV 513. A Potential Risk of Inadequate Prognosis in Hypothermic Children after Asphyxia with Delayed Abnormalities in Diffusion-Weighted Images
Lemke, Johannes
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies
Lenz, Dominic
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
Leppich, Katalin
P 451. Clinical Presentation of Children and Adolescents with Neurofibromatosis Type I
Leypoldt, Frank
FV 1016. Antibodies against Neurofascin Are Associated with Severe und Chronic Forms of Guillain–Barré’s Syndrome
Lidzba, Karen
FV 695. Does Early Postnatal hCMV Infection Have Long-Term Consequences on Brain Structure of Former Preterm Born Children?
FV 930. Reduced Structural Connectivity in Nonmotor Networks in Children Born Preterm
Liehr, Thomas
P 366. 7q11.23 Microduplication Syndrome: Neurophysiological and Neuroradiological Insights into a Rare Chromosomal Disorder
Likhite, Shibi
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones
Lindner, Martin
FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
Lingnau, Anja
P 648. The Influence of Secondary Untethering on Bladder Function of Spina Bifida Patients
Lischetzki, Grischa
P 1155. Focal Epilepsy Difficult to Treat in Hermann–Pallister’s Syndrome (KBG Syndrome)
Lochmüller, Hanns
P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries
Lock, Michael
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Lowes, Linda P.
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones
Lücke, Thomas
P 235. Short-Term Effects of Lunch with Varying Glycemic Index on Children’s Cognitive Function—CogniDo GI-II
P 1032. Cognitive Development in Children with Rolandic Epilepsy or Rolandic EEG Pattern—Preliminary Results of a Prospective Follow-up Study
FV 969. Transplantation Surgery Used Autologous Transgenic Keratinocyte Cultures Which Regenerated an Entire, Fully Functional Epidermis
P 329. Patients with Juvenile Huntington’s Disease Benefit from Early Diagnosis
P 564. Psychosocial Surrounding as an Important Influencing Factor with Hereditary Sensory and Autonomic Neuropathy—Two Case Reports
P 326. Developments in Stem Cell Transplantation in Lysosomal Storage Diseases—An Update on the Example of Mucopolysaccharidoses
P 736. Benign Enlargement of Subarachnideal Spaces and Subdural Hematoma in an Infant: Spontaneous Bleeding, Child Abuse, or Bleeding Disorder?
Luedecke, Hermann Josef
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
Luperi, Ilaria
P 1086. Role of PTRH2 in Cerebellar Development
Lüsebrink, Natalia
P 587. Osmotic Myelinolysis—A Rare but Severe Complication of Diabetic Ketoacidosis
Lütschg, Jürg
FV 113. Electrophysiological Diagnostic of Neuromuscular Diseases in Newborns, Infants, and Toddlers
Lutz, Thomas
P 520. Unclear Strokes in Pediatrics—Adenosine Deaminase 2 (ADA2) Deficiency as a Therapeutic Relevant Differential Diagnosis to Acquired Inflammatory CNS Diseases
L’italien, James
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones