Hemiplegic migraine and MRI sequences: The keys to diagnose a stroke mimic? [0.03%]
半身瘫痪型偏头痛和MRI序列：诊断假性卒中的关键吗？
E Diab,J Paurise,A Delval et al.
E Diab et al.
French guidelines for the diagnostic and management of MOG antibody-associated disease [0.03%]
MOG抗体相关疾病的诊断和管理的法国指南
L Giorgi,R Marignier,J Pique et al.
L Giorgi et al.
MOG antibody-associated disease (MOGAD) is a new entity within the spectrum of autoimmune inflammatory diseases of the central nervous system. It is distinct from multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). A...
Practice Guideline
Revue neurologique. 2025 Jun 9:S0035-3787(25)00536-3. DOI:10.1016/j.neurol.2025.04.012 2025
Data linkage between the French multiple sclerosis cohort (OFSEP) and the French national health insurance database (SNDS) [0.03%]
法国多发性硬化症队列（OFSEP）与法国国家健康保险数据库（SNDS）的数据链接
E Leray,E Drezen,R Casey et al.
E Leray et al.
Background: Linking disease registries to nationwide healthcare administrative databases increases the research opportunities. Recent guidelines emphasize the need of transparency in this process. ...
Clinical trial knowledge in families of children with epilepsy. A survey from a French Center for Rare Epilepsies [0.03%]
儿童癫痫家庭中的临床试验知识调查——来自法国罕见癫痫中心的报告
B Semal,S Höhn,V Agostini et al.
B Semal et al.
Clinical trials are essential to the development of innovative treatments. Many patients and families have limited knowledge of biomedical research. This study aimed to determine whether families of children with epilepsy were interested in...
MRI features of pleomorphic xanthoastrocytoma defined by DNA methylation profile [0.03%]
基于DNA甲基化谱的多形性黄色星形细胞瘤的磁共振影像特征分析
R Fawaz,O Aboubakr,F N El Sissy et al.
R Fawaz et al.
Introduction: Pleomorphic xanthoastrocytomas (PXA) are primary brain tumors challenging to diagnose due to their morphological and molecular overlap with other tumors. While DNA methylation profiling (MP) aids pathologica...
French guidelines for the diagnosis and management of pure hereditary spastic paraplegia [0.03%]
法国遗传性痉挛性截瘫诊断和管理指南
L Mania-Pâris,C Ewenczyk,G Nicolas et al.
L Mania-Pâris et al.
Introduction: Hereditary spastic paraplegia (HSP) describes a group of rare genetic neurological diseases characterized by a common clinical presentation made of progressive motor weakness and spasticity of the lower limb...
Practice Guideline
Revue neurologique. 2025 May 30:S0035-3787(25)00521-1. DOI:10.1016/j.neurol.2025.05.001 2025
Autosomal dominant distal myopathy due to p.Ser85Cys mutation in the MATR3 gene: Novel case series and literature review [0.03%]
MATR3基因p.Ser85Cys突变所致的常染色体显性远端肌病：新型病例系列和文献综述
D M Chitimus,N Venturelli,C Lefeuvre et al.
D M Chitimus et al.
Introduction: Matrin-3 autosomal dominant myopathy, most commonly caused by a Ser85Cys (S85C) missense mutation, is a rare distal myopathy, presenting a heterogeneous phenotype. ...
The revolution has begun [0.03%]
革命已经开始
S Dupont,S Rheims
S Dupont
Epileptic seizures recorded with microelectrodes: A persistent multiscale gap between neuronal activity, micro-, and macro-LFP? [0.03%]
微电极记录的癫痫发作：神经元活动与微局灶和宏观局灶场电位之间存在持久的多尺度差异吗？
P Calvat,E J Barbeau,A Darves-Bornoz et al.
P Calvat et al.
The cascade of events that occur in the human brain, from neurons to local circuits and global network dynamics during epileptic seizures, is barely understood. Ictogenesis in humans has been described in relation to electrophysiological co...
The safety of COVID-19 vaccines in a large French series of patients with neuromuscular conditions and the impacts of vaccination on their daily lives [0.03%]
法国神经肌肉疾病患者COVID-19疫苗安全性的大型研究及疫苗接种对患者日常生活的影响
M Barnay,A Foubert-Samier,M-H Violleau et al.
M Barnay et al.
This prospective observational study assessed how well patients with neuromuscular disorders (NMDs) tolerated coronavirus disease 2019 (COVID-19) vaccination, and the safety thereof. Patients treated in 55 expert centres of the French NMD (...