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The Lancet. Neurology
|
December 4, 2018
LRP10 in α-synucleinopathies
Chang-He Shi, Hai-Yang Luo, Yu Fan, et al.
Cell Death & Disease
|
June 30, 2017
Necroptosis in neurodegenerative diseases: a potential therapeutic target
Shuo Zhang, Mi-Bo Tang, Hai-Yang Luo, et al.
Frontiers in Aging Neuroscience
|
February 27, 2025
Study insights in the role of PGC-1α in neurological diseases: mechanisms and therapeutic potential
Mi-Bo Tang, Yi-Xuan Liu, Zheng-Wei Hu, et al.
Neuropeptides
|
June 17, 2017
Arginine vasopressin relates with spatial learning and memory in a mouse model of spinocerebellar ataxia type 3
Hong-Bo Jiang, Ai-Lin Du, Hai-Yang Luo, et al.
Parkinsonism & Related Disorders
|
September 21, 2017
TGM6 gene mutations in undiagnosed cerebellar ataxia patients
Zhi-Hua Yang, Meng-Meng Shi, Yu-Tao Liu, et al.
Neurology
|
July 3, 2015
Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation
Chang-He Shi, Bo Song, Hai-Yang Luo, et al.
Neuromuscular Disorders : NMD
|
July 1, 2019
Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates
Hai-Yang Luo, Lu Zhao, Cheng-Yuan Mao, et al.
Neurobiology of Aging
|
April 17, 2016
MC1R variants in Chinese Han patients with sporadic Parkinson's disease
Chang-He Shi, Hui Wang, Cheng-Yuan Mao, et al.
Frontiers in Molecular Neuroscience
|
July 19, 2019
Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3
Zhi-Hua Yang, Chang-He Shi, Li-Na Zhou, et al.
Scientific Reports
|
May 20, 2024
Novel inflammatory and insulin resistance indices provide a clue in cerebral amyloid angiopathy
Hang-Hang Zhu, Yun-Chao Wang, Liu-Chang He, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
The Lancet. Neurology
|
December 4, 2018
LRP10 in α-synucleinopathies
Chang-He Shi, Hai-Yang Luo, Yu Fan, et al.
Cell Death & Disease
|
June 30, 2017
Necroptosis in neurodegenerative diseases: a potential therapeutic target
Shuo Zhang, Mi-Bo Tang, Hai-Yang Luo, et al.
Frontiers in Aging Neuroscience
|
February 27, 2025
Study insights in the role of PGC-1α in neurological diseases: mechanisms and therapeutic potential
Mi-Bo Tang, Yi-Xuan Liu, Zheng-Wei Hu, et al.
Neuropeptides
|
June 17, 2017
Arginine vasopressin relates with spatial learning and memory in a mouse model of spinocerebellar ataxia type 3
Hong-Bo Jiang, Ai-Lin Du, Hai-Yang Luo, et al.
Parkinsonism & Related Disorders
|
September 21, 2017
TGM6 gene mutations in undiagnosed cerebellar ataxia patients
Zhi-Hua Yang, Meng-Meng Shi, Yu-Tao Liu, et al.
Neurology
|
July 3, 2015
Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation
Chang-He Shi, Bo Song, Hai-Yang Luo, et al.
Neuromuscular Disorders : NMD
|
July 1, 2019
Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates
Hai-Yang Luo, Lu Zhao, Cheng-Yuan Mao, et al.
Neurobiology of Aging
|
April 17, 2016
MC1R variants in Chinese Han patients with sporadic Parkinson's disease
Chang-He Shi, Hui Wang, Cheng-Yuan Mao, et al.
Frontiers in Molecular Neuroscience
|
July 19, 2019
Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3
Zhi-Hua Yang, Chang-He Shi, Li-Na Zhou, et al.
Scientific Reports
|
May 20, 2024
Novel inflammatory and insulin resistance indices provide a clue in cerebral amyloid angiopathy
Hang-Hang Zhu, Yun-Chao Wang, Liu-Chang He, et al.
Page
of 2