Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Bingwei Peng"'
Autor:
Xiaojing Li, Wenlin Wu, Yiru Zeng, Wenxiao Wu, Chi Hou, Haixia Zhu, Yinting Liao, Yang Tian, Zongzong Chen, Bingwei Peng, Wen-Xiong Chen
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease of the central nervous system. Relapse and incomplete recovery from relapse are common in NMOSD. Most patients with NMOSD have IgG to aquaporin-4 (AQP4-IgG). New biological a
Externí odkaz:
https://doaj.org/article/83033c8d0436439984a7758a7b163793
Autor:
Xiaojing Li, Wenlin Wu, Chi Hou, Yiru Zeng, Wenxiao Wu, Lianfeng Chen, Yinting Liao, Haixia Zhu, Yang Tian, Bingwei Peng, Kelu Zheng, Kaili Shi, Ying Li, Yuanyuan Gao, Yani Zhang, Haisheng Lin, Wen-Xiong Chen
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
ObjectiveTo study the clinical features of children diagnosed with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in southern China.MethodsClinical data of children diagnosed with MOGAD from April 2014 to September 2021 were
Externí odkaz:
https://doaj.org/article/e98581bf93f24add97c71cea428d87ba
Autor:
Xiaojing Li, Bingwei Peng, Chi Hou, Jinliang Li, Yiru Zeng, Wenxiao Wu, Yinting Liao, Yang Tian, Wen-Xiong Chen
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Mitochondrial encephalomyopathy caused by bi-allelic deleterious variants in TARS2 is rare. To date, only two pedigrees were reported in the literature and the connection between the gene and disease needs further study. Case pres
Externí odkaz:
https://doaj.org/article/18408702358b489ab1cac951ac4218a1
Autor:
Haixia Zhu, Wenlin Wu, Lianfeng Chen, Chi Hou, Yiru Zeng, Yang Tian, Huiling Shen, Yuanyuan Gao, Yani Zhang, Bingwei Peng, Wen-Xiong Chen, Xiaojing Li
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objective: To study the clinical characteristics and treatment of pediatric opsoclonus-myoclonus syndrome (OMS).Methods: We analyzed the clinical data of nine children OMS between June 2017 and Nov 2020.Results: Nine children (M/F = 3:6, median onset
Externí odkaz:
https://doaj.org/article/d62ddfcd3e3d48fd9a6fd353ed545bea
Autor:
Binbin Cao, Bingwei Peng, Yang Tian, Xiuying Wang, Xiaojing Li, Haixia Zhu, Huiling Shen, Wenxiong Chen
Publikováno v:
Turkish Journal of Pediatrics; Mar/Apr2024, Vol. 66 Issue 2, p191-204, 14p
Autor:
Chi Hou, Yiru Zeng, Yang Tian, Hai-xia Zhu, Yinting Liao, Hui-ling Shen, Wenlin Wu, Lianfeng Chen, Yuan-yuan Gao, Bingwei Peng, Wen-Xiong Chen, Xiaojing Li
Publikováno v:
SSRN Electronic Journal.
Autor:
Huici Liang, Wei Liang, Wen-Xiong Chen, Jia-Ling Li, Xiaojing Li, Xiuying Wang, Bingwei Peng, Haixia Zhu
Publikováno v:
Brain Topography. 33:375-383
To evaluate the effects of electrical status epilepticus during sleep (ESES) on cerebral blood flow (CBF) and explore the associated neuro-vascular coupling and neuropsychological deficits. 19 ESES patients were recruited to undergo real-time transcr
Autor:
Lianfeng Chen, Bingwei Peng, Xiaojing Li, Yang Tian, Chi Hou, Huiling Shen, Yiru Zeng, Yuanyuan Gao, Yani Zhang, Wen-Xiong Chen, Wenlin Wu, Haixia Zhu
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology, Vol 12 (2021)
Objective: To study the clinical characteristics and treatment of pediatric opsoclonus-myoclonus syndrome (OMS).Methods: We analyzed the clinical data of nine children OMS between June 2017 and Nov 2020.Results: Nine children (M/F = 3:6, median onset
Autor:
Chi Hou, Xiuying Wang, Yuanyuan Gao, Lianfeng Chen, Kelu Zheng, Haisheng Lin, Shuyao Ning, Yani Zhang, Sida Yang, Bingwei Peng, Wen-Xiong Chen, Yinting Liao, Yang Tian, Wenlin Wu, Kaili Shi, Xiaojing Li, Haixia Zhu, Yiru Zeng
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Frontiers in Neurology
Objective: Recent studies found that changes of thyroid antibodies (ATAbs), thyroid hormone, and non-thyroidal illness syndrome (NTIS) characterized by thyroid hormone inactivation with low triiodothyronine and high reverse triiodothyronine followed
Autor:
Yang Tian, Jinliang Li, Xiaojing Li, Yiru Zeng, Bingwei Peng, Wen-Xiao Wu, Wenxiong Chen, Chi Hou, Yinting Liao
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Mitochondrial encephalomyopathy caused by bi-allelic deleterious variants in TARS2 is rare. To date, only two pedigrees were reported in the literature and the connection between the gene and disease needs further study. Case presentation