Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Chong, Yan"'
Publikováno v:
BMJ case reports. 14(11)
Primary amyloidosis is a rare systemic disorder often associated with multiple organ dysfunction. The most common form, light chain amyloidosis, has an estimated age-adjusted incidence of 5.1–12.8 cases per million person-years. Spine involvement i
Autor:
Lei Zhou, Sushan Luo, Jie Lin, Wenhua Zhu, Jiahong Lu, Yufan Zhou, Jun Lu, Jianying Xi, Chong Yan, Xinyu Gu, Chongbo Zhao, Xiao Huan, Huahua Zhong
Publikováno v:
Muscle & Nerve. 63:824-830
Introduction/aims The study aims to investigate the short-term efficacy of low-dose rituximab and its effect on immunological biomarker levels in myasthenia gravis (MG) patients with antibodies against muscle-specific tyrosine kinase (MuSK-MG). Metho
Autor:
Chong Yan, Xiao Huan, Jianying Xi, Yiqi Liu, Chongbo Zhao, Sushan Luo, Jie Song, Kai Qiao, Jiahong Lu
Publikováno v:
Journal of Clinical Neuroscience. 76:161-165
Congenital myasthenic syndrome (CMS) caused by mutations in MUSK is very rare and the genotype-phenotype relationship in MUSK related CMS is still unclear. Here we identified two patients carrying a homozygous hotspot mutation, c.308A > G in MUSK fro
Autor:
Jie Song, Chong Yan, Xuelin Feng, Lei Zhou, Jun Lu, Kai Qiao, Xiao Huan, Hui Wu, Jianying Xi, Chongbo Zhao, Jiahong Lu, Sushan Luo
Publikováno v:
European Neurology. 83:182-188
Introduction: The conversion rate from ocular myasthenia gravis (OMG) to generalized myasthenia gravis (GMG) was reported to be much lower in Asian population since most OMG patients are juvenile onset. However, the exact conversion rate for adult-on
Autor:
Chong Yan, Shuizhen Zhou, Wenhui Li, Yuehua Gu, Xiaoni Liu, Hui Wu, Xuelin Feng, Jianying Xi, Chongbo Zhao, Jie Song
Publikováno v:
Journal of Clinical Neuroscience. 59:179-184
To compare HLA typing between juvenile- and adult-onset myasthenia gravis (MG), we enrolled 101 children (age ≤12 years) and 168 adults (age ≥20 years) with MG. We excluded patients with histories of thymoma, thyroid disease, or other autoimmune
Autor:
Jue Liu, Yan Wang, Chong Yan, Zhangyang Wang, Hui Wu, Sisi Jing, Jianying Xi, Chongbo Zhao, Jie Song, Liang Wang
Publikováno v:
European neurology. 83(5)
Objectives: The aim of this study wasto investigate the efficacy of tacrolimus treatment in patients with refractory generalized myasthenia gravis (MG) and explore its impact on lymphocytic phenotypes and related cytokines mRNA expression. Methods: A
Autor:
Jun Lu, Wenhua Zhu, Chongbo Zhao, Huahua Zhong, Jie Song, Jie Lin, Yafang Xu, Jianying Xi, Chong Yan, Xiao Huan, L. Zhou, Jiahong Lu, Zhiguo Lv, Sushan Luo, Kai Qiao
Publikováno v:
European neurology. 81(5-6)
Introduction: Myasthenic crisis (MC) is a life-threatening condition usually occurred in patients with myasthenia gravis (MG). Objective: On the basis of a retrospective case series review, we try to develop a scoring system to evaluate the probabili
Autor:
Zhiming Chen, Chongbo Zhao, Liang Wang, Jianyong Ding, Yang Song, Ji Chen, Jianying Xi, Chun Jin, Yongjun Zhu, Chong Yan, Jie Song
Background Myasthenia gravis (MG) is a group of autoimmune disease which could be accompanied by thymoma. Many differences have been observed between thymoma-associated MG (TAMG) and non-MG thymoma (NMG). However, the molecular difference between the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73385ffce4c23e7474251cc117716faf
https://europepmc.org/articles/PMC6626793/
https://europepmc.org/articles/PMC6626793/
Autor:
Chongbo Zhao, Xuelin Feng, Shuizhen Zhou, Wenhui Li, Jianying Xi, Jie Song, Jiahong Lu, Chong Yan
Publikováno v:
Pediatric neurology. 98
Background Patients in China with juvenile-onset myasthenia gravis present early, with a high prevalence of purely ocular symptoms, spontaneous remission rates, and low antibody seropositivity. Antibody detection using a cell-based assay has been rep
Autor:
Chong Yan, Jianying Xi, Jie Song, Chongbo Zhao, Sushan Luo, Wenhui Li, Xuelin Feng, Huahua Zhong, Rui Zhao, Shuizhen Zhou
Publikováno v:
Journal of Neuroimmunology. 349:577403
Juvenile-onset myasthenia gravis (JOMG) is a unique clinical subtype in China, featured by a higher prevalence of ocular myasthenia gravis (OMG), higher seronegativity of acetylcholine receptor (AChR) antibodies, and better prognosis than that in adu