Olayiwola Bolaji,Yasemin Bahar,Sameer Lohana et al.
Olayiwola Bolaji et al.
Heart failure (HF) and neurocognitive frailty (NCF) represent an increasingly recognized clinical intersection with profound implications for patient outcomes. Recent epidemiological data reveal that 40-60% of HF patients experience cogniti...
Efgartigimod for the treatment of Lambert-Eaton syndrome: a case report [0.03%]
伊非格拉司汀治疗兰伯特-伊顿综合征的疗效观察：病例报告
Lili Zhang,Yun Chen,Ming Hu et al.
Lili Zhang et al.
Rituximab in pathologically confirmed sarcoidosis affecting the central nervous system: a multi-center retrospective study [0.03%]
利妥昔单抗治疗病理确诊的中枢神经系统血管周围淋巴细胞浸润综合征疗效的多中心回顾性研究
Spencer K Hutto,Denis Balaban,Zachery Rohm et al.
Spencer K Hutto et al.
Background: Rituximab, a monoclonal antibody that depletes B cells by targeting CD20, has been suggested as a treatment option for neurosarcoidosis, but evidence to support its use is limited. ...
Multicenter Study
Journal of neurology. 2025 Jul 18;272(8):519. DOI:10.1007/s00415-025-13209-7 2025
Sex differences in antiseizure medications response in people with epilepsy: a systematic review [0.03%]
癫痫患者的抗惊厥药物治疗反应的性别差异：系统性综述
Loretta Giuliano,Elena Zambrelli,Vania Durante et al.
Loretta Giuliano et al.
Purpose: As a part of a wider project aimed to assess sex-related differences in adverse effects and efficacy of antiseizure medications (ASMs), we performed a systematic review focusing on differences in response to ASMs...
Małgorzata Górecka-Politańska,Krystyna Makowska,Sławomir Gonkowski
Małgorzata Górecka-Politańska
New genotype-phenotype correlations and transcriptomic findings in limb-girdle muscular dystrophy R9 [0.03%]
肌营养不良症R9的新的基因型表型相关性及转录组发现
Qingyue Yuan,Zhihao Xie,Yunlong Lu et al.
Qingyue Yuan et al.
Objective: We aimed to comprehensively investigate the clinical, genetic, muscle imaging, and pathological characteristics of limb-girdle muscular dystrophy R9 (LGMDR9) in a large cohort of Chinese patients. In addition, ...
Prevalence of hereditary transthyretin amyloidosis in CIDP patients with red flags: a multicenter genetic screening and misdiagnosis analysis [0.03%]
CIDP红旗下遗传性转甲状腺素蛋白淀粉样变性的患病率：多中心基因筛查和误诊分析
Pietro Emiliano Doneddu,Giulia Moretti,Vincenzo Di Stefano et al.
Pietro Emiliano Doneddu et al.
Background: Hereditary transthyretin amyloidosis (ATTRv) is a rare, multisystemic disorder often presenting with peripheral neuropathy and can be misdiagnosed with chronic inflammatory demyelinating polyradiculoneuropathy...
Multicenter Study
Journal of neurology. 2025 Jul 16;272(8):515. DOI:10.1007/s00415-025-13218-6 2025
Charcot-Marie-Tooth-like presentation in giant axonal neuropathy: clinical variability and prevalence in a large Japanese case series [0.03%]
日本大样本病例系列中巨轴索神经病的Charcot-Marie-Tooth样表现：临床异质性和患病率
Takahiro Hobara,Masahiro Ando,Yujiro Higuchi et al.
Takahiro Hobara et al.
Background: Giant axonal neuropathy 1 (GAN) is a rare neurodegenerative disorder with autosomal recessive inheritance and significant phenotypic heterogeneity, ranging from milder presentations resembling Charcot-Marie-To...
Longitudinal evaluation of serum neurofilament light levels in normal healthy volunteers: defining a threshold of concern [0.03%]
正常健康志愿者血清神经丝轻链水平纵向评估：确定值得关注的阈值
Thomas A Lanz,Klemens Ruprecht,Christopher J Somps et al.
Thomas A Lanz et al.
Neurofilament light (NfL) is a neuron-specific protein integral to neuronal cytoskeletons. Upon damage to the central or peripheral nervous system (NS), NfL is released into cerebrospinal fluid and blood. Elevated serum or plasma NfL levels...
Vestibular event monitoring in acute posterior circulation stroke: from emergency room to stroke unit and beyond [0.03%]
急性后循环卒中的前庭事件监测：从急诊室到卒中单元及其他阶段的监测
Gülden Akdal,Benjamin Nham,Belinda Kwok et al.
Gülden Akdal et al.