Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Zhang‐Yu Zou"'
Autor:
Chun-Zuan Xu, Xiao Huan, Su-Shan Luo, Hua-Hua Zhong, Chong-Bo Zhao, Yan Chen, Zhang-Yu Zou, Sheng Chen
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28553- (2024)
Background: Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder, characterized by progressive limb weakness, dysphagia, dysphonia, and respiratory failure due to degeneration of upper and lower motor neurons. The pathogene
Externí odkaz:
https://doaj.org/article/554dc187b5194c52ad04dca8b2997bcf
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Externí odkaz:
https://doaj.org/article/c7027780aa234ee68a962d971d62505f
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Background and AimsCurrent knowledge on the temporal dynamics of the brain functional organization in amyotrophic lateral sclerosis (ALS) is limited. This is the first study on alterations in the patterns of dynamic functional connection density (dFC
Externí odkaz:
https://doaj.org/article/9e29c0aaedc04f659dd4969211fc4773
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Mutations in the valosin-containing protein (VCP) gene have been linked to amyotrophic lateral sclerosis (ALS) in the Caucasian populations. However, the phenotype of VCP mutations in Chinese patients with (ALS) remains unclear. Targeted next-generat
Externí odkaz:
https://doaj.org/article/b9443d60e5f84199a1324602f37081fc
Autor:
Ying-Qian Lu, Jian-Min Chen, Han Lin, Shu-Yan Feng, Chun-Hui Che, Chang-Yun Liu, Hua-Pin Huang, Zhang-Yu Zou
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
TANK-binding kinase 1 (TBK1) has been identified as a causative gene of amyotrophic lateral sclerosis (ALS) in the Caucasian population in 2015. Here, we sequenced for TBK1 variants in a cohort of 15 familial ALS (fALS) and 275 sporadic ALS (sALS) of
Externí odkaz:
https://doaj.org/article/84fe27d9a7f048a6aaeeb571bfa6e91d
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Purpose: Static and dynamic analyses for identifying functional connectivity (FC) have demonstrated brain dysfunctions in amyotrophic lateral sclerosis (ALS). However, few studies on the stability of dynamic FC have been conducted among ALS patients.
Externí odkaz:
https://doaj.org/article/f9ab8568b2704b01b6b53d94c35212d9
Autor:
Shu‐Man Feng, Chun‐Hui Che, Shu‐Yan Feng, Chang‐Yun Liu, Liu‐Yi Li, Yuan‐Xiao Li, Hua‐Pin Huang, Zhang‐Yu Zou
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 12, Pp 2377-2383 (2019)
Abstract Objective Mutations in optineurin (OPTN) have been identified in familial and sporadic amyotrophic lateral sclerosis (ALS). We screened a cohort of Chinese patients for mutations in optineurin. We also performed an extensive literatures revi
Externí odkaz:
https://doaj.org/article/6a46c934631e4159b210d9f09ff77220
Autor:
Hua-Jun Chen, Chuanyin Zhan, Li-Min Cai, Jia-Hui Lin, Min-Xiong Zhou, Zhang-Yu Zou, Xu-Feng Yao, Yan-Juan Lin
Publikováno v:
NeuroImage: Clinical, Vol 32, Iss , Pp 102863- (2021)
Background: White matter (WM) impairment is a hallmark of amyotrophic lateral sclerosis (ALS). This study evaluated the capacity of mean apparent propagator magnetic resonance imaging (MAP-MRI) for detecting ALS-related WM alterations. Methods: Diffu
Externí odkaz:
https://doaj.org/article/958151db1b4a494ea993d190727fad14
Autor:
Jia-Hui Lin, Nao-Xin Huang, Chuanyin Zhan, Hua-Jun Chen, Li-Min Cai, Zhang-Yu Zou, Min-Xiong Zhou, Yuan-Fen Liu
Publikováno v:
Academic Radiology. 29:S141-S146
Rationale and Objectives To investigate the microperfusion and water molecule diffusion alterations in sensorimotor-related areas in amyotrophic lateral sclerosis (ALS) using intravoxel incoherent motion (IVIM) magnetic resonance imaging. Materials a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45cefd828bfc3170ccb1fe1454068583
https://doi.org/10.1016/j.acra.2021.07.006
https://doi.org/10.1016/j.acra.2021.07.006
Spinocerebellar ataxia type 11 (SCA11) is a rare disease and tau tubulin kinase 2 (TTBK2) gene was the causative gene. To date, only seven SCA11 families have been reported. Here, we reported a Chinese SCA11 pedigree with cerebellar ataxia. Both pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::008d79fe6cace8df5ecf61fbb2e50479
https://doi.org/10.21203/rs.3.rs-2618458/v1
https://doi.org/10.21203/rs.3.rs-2618458/v1
