Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Zhe-Long Liu"'
Autor:
Chun-Qiong Ran, Ying Su, Jin Li, Kun Wu, Zhe-Long Liu, Yan Yang, Mu-Xun Zhang, Gang Yuan, Xue-Feng Yu, Wen-Tao He
Publikováno v:
Annals of Medicine, Vol 56, Iss 1 (2024)
Background Cushing’s syndrome (CS) is associated with increased risk for heart failure, which often initially manifests as left ventricular diastolic dysfunction (LVDD). In this study, we aimed to explore the potential risk factors of LVDD in CS by
Externí odkaz:
https://doaj.org/article/74192f6a130147e4ac7299e3f50f0e57
Autor:
Dan-Pei Li, Li Huang, Ran-Ran Kan, Xiao-Yu Meng, Shu-Yun Wang, Hua-Jie Zou, Ya-Ming Guo, Pei-Qiong Luo, Li-Meng Pan, Yu-Xi Xiang, Bei-Bei Mao, Yu-Yu Xie, Zhi-Han Wang, Min Yang, Rui He, Yan Yang, Zhe-Long Liu, Jun-Hui Xie, De-Lin Ma, Ben-Ping Zhang, Shi-Ying Shao, Xi Chen, Si-Miao Xu, Wen-Tao He, Wen-Jun Li, Yong Chen, Xue-Feng Yu
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-17 (2023)
Abstract Inhibition of immunocyte infiltration and activation has been suggested to effectively ameliorate nonalcoholic steatohepatitis (NASH). Paired immunoglobulin-like receptor B (PirB) and its human ortholog receptor, leukocyte immunoglobulin-lik
Externí odkaz:
https://doaj.org/article/99b5851b521946b39aad1f9dba32b05e
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
BackgroundThrombocytopenia and poor prognosis in severe conditions are associated. However, the clinical significance of thrombocytopenia in pyogenic liver abscess (PLA) has not been evaluated.ObjectiveTo evaluate the association between thrombocytop
Externí odkaz:
https://doaj.org/article/095e81daa2c842b7bb0ca59b99294286
Autor:
Ying Su, Chun-Qiong Ran, Zhe-Long Liu, Yan Yang, Gang Yuan, Shu-Hong Hu, Xue-Feng Yu, Wen-Tao He
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Stickler syndrome (SS) is a group of hereditary collagenopathies caused by a variety of collagen and non-collagen genes. Affected patients have characteristic manifestations involving ophthalmic, articular, craniofacial and auditory disor
Externí odkaz:
https://doaj.org/article/0651f81d43d04cea899c7b6b3d73ce42
Autor:
Ying Su, Chun-Qiong Ran, Zhe-Long Liu, Yan Yang, Gang Yuan, Shu-Hong Hu, Xue-Feng Yu, Wen-Tao He
Background Stickler syndrome (SS) is a group of hereditary collagenopathies caused by a variety of collagen and non-collagen genes. Affected patients have characteristic manifestations involving ophthalmic, articular, craniofacial and auditory disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0769c78f138ceb2a4a3f12e9e7acd3e4
https://doi.org/10.21203/rs.3.rs-2298863/v1
https://doi.org/10.21203/rs.3.rs-2298863/v1
Autor:
Qian YIN, Jiang-tao YAN, Xia HAN, Wu DUAN, Jin-wen LIU, Yi-ping WU, Jian-jun LI, Zhe-long LIU
Publikováno v:
Medical Journal of Chinese People's Liberation Army, Vol 43, Iss 7, Pp 616-620 (2018)
Objective To analyze the clinical characteristics, diagnosis and treatment of Madelung's disease, and to improve the understanding of it. Method A case of type 1 Madelung's disease was reported and discussed with literature review. Results A 54-year-
Publikováno v:
Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih. 21(2)
To investigate the influence of vitamin D receptor (VDR) gene polymorphisms on susceptibility to type 1 diabetes mellitus (T1DM) in the Chinese Han population.One hundred and thirty-six Chinese Han people, including 54 T1DM patients and 82 unrelated