Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Yu-Zhou Guan"'
Autor:
Jun Ni, Miao Huang, Li Zhang, Nan Wu, Chun‐Xue Bai, Liang‐An Chen, Jun Liang, Qian Liu, Jie Wang, Yi‐Long Wu, Feng‐Chun Zhang, Shu‐Yang Zhang, Chun Chen, Jun Chen, Wen‐Tao Fang, Shu‐Geng Gao, Jian Hu, Tao Jiang, Shan‐Qing Li, He‐Cheng Li, Yong‐De Liao, Yang Liu, De‐Ruo Liu, Hong‐Xu Liu, Jian‐Yang Liu, Lun‐Xu Liu, Meng‐Zhao Wang, Chang‐Li Wang, Fan Yang, Yue Yang, Lan‐Jun Zhang, Xiu‐Yi Zhi, Wen‐Zhao Zhong, Yu‐Zhou Guan, Xiao‐Xiao Guo, Chun‐Xia He, Shao‐Lei Li, Yue Li, Nai‐Xin Liang, Fang‐Liang Lu, Chao Lv, Wei Lv, Xiao‐Yan Si, Feng‐Wei Tan, Han‐Ping Wang, Jiang‐Shan Wang, Shi Yan, Hua‐Xia Yang, Hui‐Juan Zhu, Jun‐Ling Zhuang, Ming‐Lei Zhuo
Publikováno v:
Thoracic Cancer, Vol 12, Iss 9, Pp 1469-1488 (2021)
Abstract Perioperative adjuvant treatment has become an increasingly important aspect of the management of patients with non‐small cell lung cancer (NSCLC). In particular, the success of immune checkpoint inhibitors, such as antibodies against PD
Externí odkaz:
https://doaj.org/article/3dab770ad14a4eb394851fdb819f7bec
Autor:
Yuan-Ren Tong, Chang Geng, Yu-Zhou Guan, Yan-Huan Zhao, Hai-Tao Ren, Feng-Xia Yao, Chao Ling, Dan-Chen Wang, Lin Chen, Li-Ying Cui, Shu-Yang Zhang, Yi Dai
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive neuromuscular disorders caused by mutations in DMD. A high-quality database of DMD/BMD is essential not only for clinical practice but also for fundamental r
Externí odkaz:
https://doaj.org/article/b39a3e834c0b4f7e9ef083687870c441
Autor:
Min QIAN, Hong-zhi GUAN, Yu-zhou GUAN, Yan-ping WEI, Man-qing XIE, Hai-tao REN, Yan-huan ZHAO, Lin CHEN
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 9, Pp 683-687 (2018)
Background Anti-CV2/CRMP5 antibodies-associated paraneoplastic peripheral neuropathy (PPN) is a poorly understood disease due to its rarity. This study aimed to summarize the clinical manifestations, electrophysiological and pathological characterist
Externí odkaz:
https://doaj.org/article/758ce13d19304d97852cbe2272d66c27
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 9, Pp 1036-1040 (2016)
Background: Single-fiber electromyography (SFEMG) has been suggested as a quantitative method for supporting chronic partial denervation in amyotrophic lateral sclerosis (ALS) by the revised EI Escorial criteria. Although concentric needle (CN) elect
Externí odkaz:
https://doaj.org/article/12e8beeff74e4a01b8cc7b27d481bf01
Autor:
Jia Fang, Ming-Sheng Liu, Yu-Zhou Guan, Hua Du, Ben-Hong Li, Bo Cui, Qing-Yun Ding, Li-Ying Cui
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 7, Pp 792-798 (2016)
Background: Amyotrophic lateral sclerosis (ALS) and some mimic disorders, such as distal-type cervical spondylotic amyotrophy (CSA), Hirayama disease (HD), and spinobulbar muscular atrophy (SBMA) may present with intrinsic hand muscle atrophy. This s
Externí odkaz:
https://doaj.org/article/a256b35c9dab4e26ae4ca9ce5739356f
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 4, Pp 515-519 (2015)
Background: In amyotrophic lateral sclerosis (ALS), repeater F waves are increased. Accurate assessment of repeater F waves requires an adequate sample size. Methods: We studied the F waves of left ulnar nerves in ALS patients. Based on the presence
Externí odkaz:
https://doaj.org/article/e1d44ca26a8647e28f195d4b399d248d
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 20, Pp 2783-2786 (2015)
Background: Single-fiber electromyography (SFEMG) abnormality in the extensor digitorum communis (EDC) was reported in ocular myasthenia gravis (OMG), which indicated subclinical involvement beyond extraocular muscles in OMG patients. The relationshi
Externí odkaz:
https://doaj.org/article/c6636a59b7d94b26bfaec388e4f89c30
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 21, Pp 2919-2925 (2015)
Background: Motor dysfunction is common in stroke patients. Clinical electrophysiological studies suggest that transsynaptic degeneration occurred in the lower motor neurons, while pathological evidence is lacked. This study aimed to combine the elec
Externí odkaz:
https://doaj.org/article/342e7243ee344250922515bb5462aa23
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 13, Pp 1738-1742 (2015)
Background: Dysfunctional spinal circuit may play a role in the pathophysiology of amyotrophic lateral sclerosis (ALS). The purpose of this study was to use F waves for assessment of segmental motoneuronal excitability following upper motor neuron (U
Externí odkaz:
https://doaj.org/article/28c55c5230ae4378a73d7fcc02ddf1cc
Autor:
Da-Wei Li, Mingsheng Liu, Bo Cui, Jia Fang, Yu-Zhou Guan, Qingyun Ding, Xiaoguang Li, Liying Cui
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0171522 (2017)
OBJECTIVES:The accurate and early diagnosis of amyotrophic lateral sclerosis (ALS) is important for extending the life expectancy of patients. However, previous studies that have assessed the diagnostic sensitivities of the Awaji criteria (AC) and th
Externí odkaz:
https://doaj.org/article/4e517371b6b54b2298cfe24a0c46ff72