Clinical Differences in Newly Diagnosed Spanish-Speaking Pediatric Epilepsy Patients: A Single-Center Examination [0.03%]
西班牙语国家新诊断的儿童癫痫患者的临床特点：单一中心调查结果分析
Chelsey Stillman,Kelly Knupp,Krista Eschbach et al.
Chelsey Stillman et al.
BackgroundEpilepsy is a common pediatric diagnosis, and recent national and international efforts aim to improve care for neurologic conditions. This study examined initial clinical differences between English- and Spanish-speaking pediatri...
Clinical and Genetic Characteristics of Children with Pelizaeus-Merzbacher Disease [0.03%]
Pelizaeus-Merzbacher病患儿的临床及基因特征分析
Haolin Chen,Chaonan Yu,Yuanhong Ji et al.
Haolin Chen et al.
Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive genetic disorder. Patients with PMD usually present with dystonia, ataxia, progressive spasms, nystagmus, and motor developmental delay, which may be misdiagnosed as cerebral dyspl...
Clinical, Neuroimaging, and Functional Profile of Children With Hemiplegic Cerebral Palsy: A Cross-Sectional Study From a Tertiary Care Center [0.03%]
儿童偏瘫型脑性瘫痪的临床、影像和功能特征：来自一家三级医疗机构的横断面研究
Tandra Harish Varma,Arushi Gahlot Saini,Pradeep Kumar Gunasekaran et al.
Tandra Harish Varma et al.
ObjectiveTo characterize the clinical profile, functional and developmental status, radiologic patterns, and comorbidity burden in children aged 1-14 years diagnosed with hemiplegic cerebral palsy (HCP) at a tertiary pediatric neurology cen...
A Gene, A Breakthrough, A Challenge: Lessons From the History of Spinal Muscular Atrophy [0.03%]
一个基因，一项突破，一个挑战——脊髓性肌萎缩症研究史给我们的启示
Kiren George Koshy,Mary Iype,Anitha Ayyappan
Kiren George Koshy
The discovery of the SMN1 gene on chromosome 5q in 1995, and later, identification of SMN2 as a modifier gene was the breakthrough in the history of spinal muscular atrophy (SMA). It was the discovery of this gene that led to the discovery ...
Global Child Neurology Capacity Building Through the Child Neurology Society International Affairs Committee: From Needs Assessment to SMART Action Goals [0.03%]
通过儿童神经学学会国际事务委员会进行全球儿童神经病学能力建设：从需求评估到SMART行动目标
Sharoon Qaiser,Alcy Torres,Jorge Vidaurre et al.
Sharoon Qaiser et al.
BackgroundChild neurology in low- and middle-income countries (LMICs) faces persistent disparities in workforce capacity, subspecialty training, and structured mentorship. To address these gaps, the Child Neurology Society International Aff...
Superfast VNS Titration for the Treatment of SRSE in the Acute Phase of FIRES: A Pediatric Case Report and Literature Review [0.03%]
超高速VNS滴定在FIRES急性期治疗SRSE的儿科病例报告及文献回顾
Yao Meng,Guifu Geng,Lin Wang et al.
Yao Meng et al.
Febrile infection-related epilepsy syndrome (FIRES) is a rare and severe epileptic encephalopathy that predominantly affects children, characterized by the sudden onset of superrefractory status epilepticus (SRSE) following a febrile infect...
Eric H Kossoff,Zahava Turner,Adam L Hartman
Eric H Kossoff
The classic ketogenic diet, a high-fat, adequate-protein, very-low-carbohydrate therapy, is a widely used, mainstream, standard of care in the management of refractory epilepsy. It is difficult to imagine that the first poster presentation ...
Using Quantitative EEG to Manage Blood Pressure in a Child With Carotid ECMO Cannulation: Case Report and Proof of Concept [0.03%]
定量EEG在颈动脉ECMO插管儿童中管理血压的案例报告及概念证明
Natalie Pierson,Natalia Lopez,Yi Li et al.
Natalie Pierson et al.
Pediatric extracorporeal membrane oxygenation (ECMO) carries a high risk of arterial ischemic stroke (AIS). AIS in patients with right common carotid artery (RCCA) cannulation may be driven by inadequate cross-lateral perfusion from the lef...
GAD65 Antibody-Associated Epilepsy and Autoimmune Encephalitis in Children and Young Adults: A Single-Center Case Series and Review of Literature [0.03%]
儿童和青年人GAD65抗体相关性癫痫及自身免疫脑病的病例系列及文献复习
Praveen Kumar Ramani,Cade M Haynie,Eniya Beemarajan et al.
Praveen Kumar Ramani et al.
Many cases of GAD65 autoimmune encephalitis are described in adults, but this is an understudied topic in children. Not many pediatric cases of GAD65 encephalitis are reported in literature and the diagnostic criteria are not well defined. ...
First-Line Rituximab in Pediatric-Onset Multiple Sclerosis: Clinical and MRI Outcomes in a Retrospective Cohort [0.03%]
一线利妥昔单抗治疗儿童期发病的多发性硬化症：回顾性队列的临床和磁共振成像结果
Hannah Lewis,Alexandra Kiss,Praveen Ramani et al.
Hannah Lewis et al.
B-cell depletion is increasingly used in pediatric-onset multiple sclerosis (POMS), but data on rituximab as first-line chronic therapy remain limited. We retrospectively reviewed 17 children with POMS who received rituximab as their initia...