Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Xingao Wang"'
Autor:
YuZhi Shi, Kang Zhang, GeHong Dong, Hua Pan, Bin Chen, An Wang, SongTao Niu, XinGao Wang, ZaiQiang Zhang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 3, Pp 800-805 (2024)
Abstract Movement disorders manifest in various hereditary neurodegenerative diseases. We reported a young man who presented with progressive upper limb dystonia, spastic tetraplegia, and ataxia. Whole‐exome sequencing (WES) revealed a novel varian
Externí odkaz:
https://doaj.org/article/b1d55e3ee0a243c29a4c4f04d12ab863
Autor:
Chen Zhang, Honghua Zheng, Xin Li, Shaowu Li, Wei Li, Ziwei Wang, Songtao Niu, Xingao Wang, Zaiqiang Zhang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 10, Pp 1586-1595 (2022)
Abstract Objective There is evidence showing both heterozygous HTRA1 and homozygous HTRA1 mutations as causal for familial cerebral small vessel disease (CSVD). The clinical and neuroimaging signs of heterozygous HTRA1‐related CSVD can mimic cerebr
Externí odkaz:
https://doaj.org/article/7784732b4cbe40d48934ea868fd3712b
Autor:
Chen Zhang, Honghua Zheng, Xin Li, Shaowu Li, Wei Li, Ziwei Wang, Songtao Niu, Xingao Wang, Zaiqiang Zhang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 7, Pp 1263-1263 (2023)
Externí odkaz:
https://doaj.org/article/6362d05e84d44d71be24107ba103d47a
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Background and PurposeA variety of hereditary diseases overlap with neurological phenotypes or even share genes with hereditary spastic paraplegia (HSP). The aim of this study was to determine the clinical features and genetic spectrum of patients wi
Externí odkaz:
https://doaj.org/article/efe05468c013471aab453dc4c35ebd33
Autor:
Bin Chen, Zaiqiang Zhang, Na Chen, Wei Li, Hua Pan, Xingao Wang, Yuting Ren, Yuzhi Shi, Hongfei Tai, Songtao Niu
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Mutations in the myelin protein zero gene are responsible for the autosomal dominant Charcot-Marie-Tooth disease (CMT). We summarized the genetic and clinical features of six unrelated Chinese families and the genetic spectrum of Chinese patients wit
Externí odkaz:
https://doaj.org/article/f6d8e57eec7144c499ff9d4b927a1e4f
Autor:
Hefei Tang, Jiayao Sun, Yu Wang, Xu Jie, Yan Ma, Anxin Wang, Yijun Zhang, Xingao Wang, Yongjun Wang
Publikováno v:
Frontiers in Neurology, Vol 11 (2021)
Background and Purpose: QT dispersion (QTd) abnormalities are widely documented in stroke patients. This study aims to investigate the association between QTd and clinical outcomes in IS patients.Methods: IS patients registered in the Blood Pressure
Externí odkaz:
https://doaj.org/article/29d4f2efa21f48108db9784f64068ccb
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background and objective: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited systemic arteriopathy, the classic feature of which is small vessel lesions. Studies on intracranial large
Externí odkaz:
https://doaj.org/article/ae351e90fd2048c983971a346eb78dd8
Autor:
Xingao Wang, Qun Wang, Hefei Tang, Bin Chen, Xiang Dong, Songtao Niu, Shaowu Li, Yuzhi Shi, Wei Shan, Zaiqiang Zhang
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
The white matter disease spectrum is associated with many genetic diseases, including AARS2, CADASIL, ALD, and others. In this study, to determine the novel alanyl-tRNA synthetase 2 mutation implicated in white matter disease, several families with a
Externí odkaz:
https://doaj.org/article/59c33664712c4510834cc282c436ceea
Autor:
YuZhi Shi, ShaoWu Li, Wei Li, Chen Zhang, LiYing Guo, YunZhu Pan, XueMei Zhou, XinGao Wang, Songtao Niu, XueYing Yu, HeFei Tang, Bin Chen, ZaiQiang Zhang
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Background and objective: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the best known and the most common monogenic small vessel disease (SVD). Cognitive impairment is an inevitable feature o
Externí odkaz:
https://doaj.org/article/3f2c86ef0e0f4fdc9cb47c174ac8e923
Autor:
Bin Chen, Jing Jing, Gehong Dong, Yuzhi Shi, Cuiping Zhang, Yumei Zhang, An Wang, Hongfei Tai, Songtao Niu, Xingao Wang, Hua Pan, Zaiqiang Zhang
Publikováno v:
Neurological Sciences. 44:1769-1772
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a86be55682f27a7cb807499c7cd63453
https://doi.org/10.1007/s10072-023-06688-x
https://doi.org/10.1007/s10072-023-06688-x