Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Chuanqiang Pu"'
Autor:
Peng Zhang, Jian He, Fei Wang, Jing Gong, Lu Wang, Qian Wu, Wenjiong Li, Hongju Liu, Jing Wang, Kunshan Zhang, Mao Li, Xusheng Huang, Chuanqiang Pu, Ying Li, Fengjie Jiang, Fudi Wang, Junxia Min, Xiaoping Chen
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 10, Iss 3, Pp 557-573 (2019)
Abstract Background Muscle wasting occurs in response to various physiological and pathological conditions, including ageing and Duchenne muscular dystrophy (DMD). Transforming growth factor‐β1 (TGF‐β1) contributes to muscle pathogenesis in eld
Externí odkaz:
https://doaj.org/article/eb74dc2601d9463aac8b59fafc111de6
Publikováno v:
Clinical Neuropathology. 40:319-327
Objective To analyze muscle histopathology of myasthenia gravis (MG) patients and further explore the underlying mechanism comparing with previous literature. Materials and methods We analyzed the clinicopathological features of 8 MG patients who had
Publikováno v:
Neurology India. 70(5)
Autor:
Xueli Chang, Zhaoxu Yin, Wei Zhang, Jiaying Shi, Chuanqiang Pu, Qiang Shi, Juan Wang, Jing Zhang, Li Yan, Wenqu Yang, Junhong Guo
Publikováno v:
Medicine. 101(41)
The pathogenesis of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS) syndrome has not been fully elucidated. The m.3243A G mutation which is responsible for 80% MELAS patients affects proteins with undetermined
Publikováno v:
Zhonghua nei ke za zhi. 61(10)
Publikováno v:
Clinical Neuropathology. 40:93-97
Aims Lambert-Eaton myasthenic syndrome (LEMS) is a kind of autoimmune disease of the neuromuscular junction that is often misdiagnosed as a peripheral nerve disease or myopathy. For some difficult cases, muscle biopsy examination is useful for differ
Publikováno v:
Clinical Neuropathology. 40:292-294
Autor:
Rui Ban, Robert Kopajtich, Junlan Lv, Sarah L Stenton, Masaru Shimura, Zhaoxia Wang, Yun Yuan, Junling Wang, Xiaodi Han, Zhimei Liu, Qiang Shi, Chuanqiang Pu, Holger Prokisch, Fang Fang, Matthias Elstner
Publikováno v:
Brain 145, e125-e127 (2022)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5319d070c4b0b5f12f7040b0853af8
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=66387
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=66387
Publikováno v:
Parkinsonism & Related Disorders. 86:58-60
SPG78 is a subtype of hereditary spastic paraplegia(HSP) caused by ATP13A2 gene mutations. SPG78 was reported as complicated HSP in several cases, but was never associated with pure HSP. Here we report the first Chinese patient carrying a novel homoz
Autor:
Simiao Wu, Bo Wu, Ming Liu, Zhengming Chen, Wenzhi Wang, Craig S Anderson, Peter Sandercock, Yongjun Wang, Yining Huang, Liying Cui, Chuanqiang Pu, Jianping Jia, Tong Zhang, Xinfeng Liu, Suming Zhang, Peng Xie, Dongsheng Fan, Xunming Ji, Ka-Sing Lawrence Wong, Longde Wang, Chenchen Wei, Yanan Wang, Yajun Cheng, Yunhai Liu, Xin Li, Qiang Dong, Jinsheng Zeng, Bin Peng, Yun Xu, Yi Yang, Yilong Wang, Gang Zhao, Wei Wang, Yuming Xu, Qingwu Yang, Zhiyi He, Shaoshi Wang, Chao You, Ying Gao, Dong Zhou, Li He, Zixiao Li, Jie Yang, Chunyan Lei, Yuhua Zhao, Junfeng Liu, Shuting Zhang, Wendan Tao, Zilong Hao, Deren Wang, Shihong Zhang
Publikováno v:
2019, ' Stroke in China: advances and challenges in epidemiology, prevention, and management ', Lancet Neurology, vol. 18, no. 4, pp. 394-405 . https://doi.org/10.1016/S1474-4422(18)30500-3
With over 2 million new cases annually, stroke is associated with the highest disability-adjusted life-years lost of any disease in China. The burden is expected to increase further as a result of population ageing, an ongoing high prevalence of risk