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S

Sali M.K. Farhan

McGill University
H指数:22
被引数:1,626

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Transcriptome-based screening in TARDBP/TDP-43 knock-in motor neurons identifies the NEDD8-activating enzyme inhibitor MLN4924

基于TARDBP/TDP-43基因敲入运动神经元的转录组筛选鉴定了NEDD8激活酶抑制剂MLN4924

2025-08-050
OA
Regional free-water diffusion is more strongly related to neuroinflammation than neurodegeneration

区域性自由水扩散与神经炎症的相关性比与神经退行性的更强。

2025-06-250
PRE
The Neurodegenerative Disease Knowledge Portal
2025-04-010
PRE
An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2

与ATXN2的CAG重复扩增相关的肌萎缩侧索硬化的多效性和渗透性的观察研究

2025-02-160
OAAI
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications

肌萎缩性侧索硬化症的寡基因结构具有基因检测,咨询和治疗意义

2025-02-130
OAAI
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature
2024-01-173
PRE
Association of plasma biomarkers with cognition, cognitive decline, and daily function across and within neurodegenerative diseases: Results from the Ontario Neurodegenerative Disease Research Initiative

血浆生物标志物与神经退行性疾病的认知,认知能力下降和日常功能的关联: 安大略省神经退行性疾病研究计划的结果

2023-12-175
OA
Rare neurovascular genetic and imaging markers across neurodegenerative diseases

跨神经退行性疾病的罕见神经血管遗传和成像标记

2023-06-053
OA
Association of Dual-Task Gait Cost and White Matter Hyperintensity Burden Poststroke: Results From the ONDRI

双任务步态成本与中风后白质高强度负担的关联: 来自ONDRI的结果

2023-06-025
OAAI
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
NEURON
IF15
2022-03-0162
OA
Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes
2022-01-192
OA