Zobrazeno 1 - 10
of 46
pro vyhledávání: '"SongTao Niu"'
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:
Jingjing Wu, Fenghua Gao, Wenhua Wang, Xudong Zhang, Meng Dong, Lei Zhang, Xin Li, Ling Li, Zhenchang Sun, Xinhua Wang, Xiaorui Fu, Linan Zhu, Mengjie Ding, Songtao Niu, Zhaoming Li, Yu Chang, Feifei Nan, Jiaqian Yan, Hui Yu, Xiaolong Wu, Zhiyuan Zhou, Jieming Zhang, Mingzhi Zhang
Publikováno v:
Cancer Biology & Medicine, Vol 19, Iss 7, Pp 1089-1099 (2022)
Objective: This study aimed to evaluate the safety, efficacy, and feasibility of the rituximab, fotemustine, pemetrexed, and dexamethasone (R-FPD) regimen followed by whole-brain radiotherapy (WBRT) for patients with primary central nervous system ly
Externí odkaz:
https://doaj.org/article/1f816c3f94d7498b8c9c79223794a35a
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
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:
Linan Zhu, Xudong Zhang, Xiaorui Fu, Zhaoming Li, Zhenchang Sun, Jingjing Wu, Xinhua Wang, Feng Wang, Xiangke Li, Songtao Niu, Mengjie Ding, Zhenzhen Yang, Wanqiu Yang, Meifeng Yin, Lei Zhang, Mingzhi Zhang
Publikováno v:
Journal of Translational Medicine, Vol 16, Iss 1, Pp 1-10 (2018)
Abstract Background Esophageal carcinoma is the eighth prevalent malignancy and ranks the sixth in carcinoma-related death worldwide. Tumor necrosis factor-α-induced protein-8 like-2 (TIPE2) has been identified as a tumor suppressor in multiple carc
Externí odkaz:
https://doaj.org/article/6f926a2511fd4522b0ee6a5eec6ecbde
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