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The International Journal of Neuroscience
|
May 9, 2012
Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds
Dandan Jia, Beisha Tang, Zhao Chen, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
March 11, 2017
Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China
Chuzheng Pan, Bin Jiao, Tingting Xiao, et al.
Neurology India
|
November 26, 2009
The correlation between magnetic resonance imaging features of the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease
Xiaochun Liang, Hong Jiang, Changqing Chen, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
October 27, 2018
Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene
Zhenhua Yuan, Lina Guo, Xixi Liu, et al.
Brain : a Journal of Neurology
|
January 1, 2016
High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China
Bin Jiao, Tingting Xiao, Lihua Hou, et al.
Journal of Human Genetics
|
January 9, 2015
Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case report
Sheng Zeng, Junsheng Zeng, Miao He, et al.
Frontiers in Neurology
|
May 23, 2022
The Clinical and Polynucleotide Repeat Expansion Analysis of <i>ATXN2, NOP56, AR</i> and <i>C9orf72</i> in Patients With ALS From Mainland China
Xiaorong Hou, Wanzhen Li, Pan Liu, et al.
Molecular Neurobiology
|
July 28, 2025
Deficiency of PLA2G6 Induces Ferroptosis in Dopaminergic Neurons and Contributes to Parkinson's Disease Pathogenesis via Disruption of PRDX6/FTH1/GPX4 Axis
Taole Li, Jiabin Liu, Xiurong Huang, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids
|
June 22, 2023
SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS
Museer A Lone, Sen Zeng, Florence Bourquin, et al.
Ebiomedicine
|
March 15, 2026
Shared genetic architecture between sleep traits and cardiometabolic diseases
Yuan Zhang, Shijie Jian, Haiyan Ouyang, et al.
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Search research articles
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Showing results (141-150 of 514) with videos related to
Sort By:
Page
of 52
The International Journal of Neuroscience
|
May 9, 2012
Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds
Dandan Jia, Beisha Tang, Zhao Chen, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
March 11, 2017
Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China
Chuzheng Pan, Bin Jiao, Tingting Xiao, et al.
Neurology India
|
November 26, 2009
The correlation between magnetic resonance imaging features of the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease
Xiaochun Liang, Hong Jiang, Changqing Chen, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
October 27, 2018
Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene
Zhenhua Yuan, Lina Guo, Xixi Liu, et al.
Brain : a Journal of Neurology
|
January 1, 2016
High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China
Bin Jiao, Tingting Xiao, Lihua Hou, et al.
Journal of Human Genetics
|
January 9, 2015
Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case report
Sheng Zeng, Junsheng Zeng, Miao He, et al.
Frontiers in Neurology
|
May 23, 2022
The Clinical and Polynucleotide Repeat Expansion Analysis of <i>ATXN2, NOP56, AR</i> and <i>C9orf72</i> in Patients With ALS From Mainland China
Xiaorong Hou, Wanzhen Li, Pan Liu, et al.
Molecular Neurobiology
|
July 28, 2025
Deficiency of PLA2G6 Induces Ferroptosis in Dopaminergic Neurons and Contributes to Parkinson's Disease Pathogenesis via Disruption of PRDX6/FTH1/GPX4 Axis
Taole Li, Jiabin Liu, Xiurong Huang, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids
|
June 22, 2023
SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS
Museer A Lone, Sen Zeng, Florence Bourquin, et al.
Ebiomedicine
|
March 15, 2026
Shared genetic architecture between sleep traits and cardiometabolic diseases
Yuan Zhang, Shijie Jian, Haiyan Ouyang, et al.
Page
of 52