Risk factors, clinical presentation, stroke subtype and short-term outcome following acute stroke in a multi-ethnic population: a 10-year study from Qatar [0.03%]
卡塔尔一个多民族群体的急性卒中的危险因素、临床表现、卒中亚型及短期预后的10年研究
Parsa Babaei Zadeh,Kim H Tran,Nabeela Khan et al.
Parsa Babaei Zadeh et al.
Background: Stroke remains a leading global cause of disability and mortality with over 100 million patients affected worldwide. Its incidence has risen in recent decades, especially in low- and middle-income countries (L...
Environmental risk factors for multiple sclerosis: a comprehensive systematic review and meta-analysis [0.03%]
多发性硬化症环境危险因素的全面系统评价和meta分析
Bruno Kusznir Vitturi,Maria Cellerino,Daniele Boccia et al.
Bruno Kusznir Vitturi et al.
Background and objectives: Multiple sclerosis (MS) is a demyelinating disease of the central nervous system. Its etiology may involve both genetic and environmental factors, including vitamin D levels, body mass index, in...
Brain functional connectivity changes in amyotrophic lateral sclerosis with apathy and depression [0.03%]
肌萎缩侧索硬化伴淡漠和抑郁患者的脑功能连接改变
Veronica Castelnovo,Elisa Canu,Silvia Basaia et al.
Veronica Castelnovo et al.
Background: Apathy and depression are the most prevalent neuropsychiatric symptoms in amyotrophic lateral sclerosis (ALS). Although insufficiently investigated, their distinction holds important clinical relevance for acc...
MOGAD-related epilepsy: a systematic characterization of age-dependent clinical, fluid, imaging and neurophysiological features [0.03%]
与MOGAD相关的癫痫：临床、液体、影像和神经生理特征的系统特征描述
Martina Rubin,Gianni Cutillo,Vittorio Viti et al.
Martina Rubin et al.
Background: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a rare central nervous system (CNS) demyelinating disease presenting heterogeneously across lifespan. Although frequent, epilepsy rema...
Neurophysiological biomarkers of networks impairment in amyotrophic lateral sclerosis [0.03%]
肌萎缩侧索硬化症网络损伤的神经生理生物标志物
Antonio Fasano,Veria Vacchiano,Luigi Bonan et al.
Antonio Fasano et al.
Amyotrophic lateral sclerosis (ALS) is a heterogeneous disease involving motor system as well as cognitive domains. There is an urgent need for objective biomarkers that can subcategorize subjects into homogeneous groups based on disease pa...
Correction: Refining the clinical and therapeutic spectrum of granulomatous myositis from a large cohort of patients [0.03%]
订正：从大量患者群体中细化肉芽肿性肌炎的临床和治疗谱系
Antonio Lauletta,Laurène de Le Hoye,Sarah Leonard-Louis et al.
Antonio Lauletta et al.
Published Erratum
Journal of neurology. 2025 Jul 12;272(8):505. DOI:10.1007/s00415-025-13020-4 2025
Tiffany Eatz,Sakir Humayun Gultekin,Namrata Sonia Chandhok et al.
Tiffany Eatz et al.
Introduction: Vacuoles, E1 enzyme, X-linked (Xp11.3), autoinflammatory, somatic (VEXAS) syndrome is a novel acquired disorder of adulthood, discovered in 2020. Neurological symptoms and sequelae of this new disease are un...
Key to better outcomes in stroke intervention: early versus complete reperfusion in first pass recanalization [0.03%]
一次再通中的彻底恢复优于早期恢复：改善卒中预后的关键因素
Alexander Heitkamp,Sophie-Maria Hierholzer,Christian Heitkamp et al.
Alexander Heitkamp et al.
Background and purpose: First pass (FP) recanalization, defined as achieving mTICI 2b or higher in a single thrombectomy attempt, has been linked to better functional recovery in acute ischemic stroke patients. This study...
Observational Study
Journal of neurology. 2025 Jul 11;272(8):504. DOI:10.1007/s00415-025-13235-5 2025
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa [0.03%]
α-半乳糖苷酶A替代治疗晚发型庞贝病患者10年和15年的意大利队列分析
T Mongini,G Gadaleta,P Alonge et al.
T Mongini et al.
Background and objectives: Late-onset Pompe disease (LOPD) is the first genetic neuromuscular disease treated with enzyme replacement therapy (ERT) in 2006, with variable results over time. This study aimed to assess ther...
Hemifacial spasm: an update on pathophysiology, investigations and management [0.03%]
半面痉挛：病理生理、检查及治疗进展
Aaron Jesuthasan,Ammar Natalwala,Indran Davagnanam et al.
Aaron Jesuthasan et al.
Hemifacial spasm (HFS) is characterized by involuntary, paroxysmal contractions of muscles innervated by the facial nerve that can lead to a negative impact on daily activities, including reading or driving, as well as psychosocial well-bei...