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期刊名:Pediatric neurology

缩写:PEDIATR NEUROL

ISSN:0887-8994

e-ISSN:1873-5150

IF/分区:2.1/Q2

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共收录本刊相关文章索引3913
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Tarrant O McPherson,E Martina Bebin,Laura S Farach et al. Tarrant O McPherson et al.
Background: The PREVeNT trial enrolled 72 infants with tuberous sclerosis complex using the presence of interictal epileptiform discharges (IEDs) on a one-h electroencephalography (EEG) to randomize into a trial of placeb...
Sujith Gurram,Carlos A Fajardo,Kyong-Soon Lee et al. Sujith Gurram et al.
Background: Hypoxic ischemic encephalopathy (HIE) leads to neonatal mortality and long-term morbidities. Clinical and histological chorioamnionitis is an additional risk factor for neonates with HIE, which could increase ...
Natalia Builes,Andres Felipe Escobar Natalia Builes
Background: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a key therapy for stabilizing neurological function and improving survival in cerebral adrenoleukodystrophy (CALD). Identifying a suitable matc...
Sara Morcos,Kristin Falbo,Laurie Seltzer et al. Sara Morcos et al.
Background: The YWHAG gene encodes a member of the 14-3-3 protein family important for cellular signaling and neuronal migration. Recent studies suggest its role in early-onset epilepsy, epileptic encephalopathy, and seiz...
Akshaya Dayal,Bharti Dhankhar,Rituparna Manna et al. Akshaya Dayal et al.
Background: Migraine is a common childhood disorder with an initial presentation occurring at any age. It affects the quality of life significantly. Over the years many studies have been done. However, there is limited re...
Antonia Herrmann,Alice Kuhn,Maren Hackenberg et al. Antonia Herrmann et al.
Background: Pontocerebellar hypoplasia type 2A (PCH2A) is a rare autosomal recessive neurodegenerative disease caused by a specific pathogenic variant in the TSEN54 gene (p.A307S). Affected children show early but initial...
Raghad Shiraz Alharthi,Muhammad Talal Alrifai,Raghad Darwish Alomari et al. Raghad Shiraz Alharthi et al.
Background: Childhood absence epilepsy (CAE) is a common pediatric epilepsy syndrome affecting school-aged children. While generally considered benign, recent studies indicate that a significant proportion of patients exp...
Corinna Klein,Camila A Ferrario,Rajsekar R Rajaraman et al. Corinna Klein et al.
Background: This study aimed to identify child and family characteristics contributing to parenting stress in parents of young children with tuberous sclerosis complex (TSC). ...