Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Chun‑Lin Gao"'
Autor:
Ying-chao Peng, Zhi-qiang Zhang, Mei-qiu Wang, Xiang Fang, Chun-lin Gao, Tao Sun, Zheng-kun Xia
Publikováno v:
Linchuang shenzangbing zazhi, Vol 24, Iss 2, Pp 108-115 (2024)
ObjectiveTo evaluate the efficacy and safety of rituximab (RTX) for steroid-resistant idiopathic focal segmental glomerulosclerosis (FSGS) in children.MethodsFrom 2014 to 2020, the relevant clinical data were retrospectively reviewed for 12 children
Externí odkaz:
https://doaj.org/article/4a82c3cbd90b4c2c9f9eda55a887a4ee
Publikováno v:
Renal Failure, Vol 45, Iss 2 (2023)
Background Acute interstitial nephritis (AIN) is a relatively rare cause of acute kidney injury (AKI) in children. Immune complex (IC) deposition was rare in renal pathology of AIN.Methods Based on the status and position of IC deposition, a total of
Externí odkaz:
https://doaj.org/article/e365a42553aa4d6792b1e9e9b56423f8
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundCrescentic glomerulonephritis (CrGN) is a relatively rare but severe condition in childhood with the clinical feature of rapidly progressive glomerulonephritis (RPGN). The aim of this study is to investigate the clinicopathological features
Externí odkaz:
https://doaj.org/article/51de584a43454f34bfc8f2a765a7da76
Autor:
Chun-lin GAO, Jia-ling WU
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 4, Pp 249-253 (2017)
Post-stroke depression (PSD) is a serious complication affecting the survival and functional recovery of stroke patients. The prevalence rate of PSD is about 30% . PSD happens mostly within one year after stroke, and especially within 3 months after
Externí odkaz:
https://doaj.org/article/c48f87f8b22c4571b63460faaa353803
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 3, Pp 209-213 (2015)
Objective To explore the effects of motor imagery (MI) combined with the third generation functional electrical stimulation (FES) on upper limb motor function in acute ischemic stroke patients with hemiplegia. Methods Forty acute ischemic stroke pati
Externí odkaz:
https://doaj.org/article/047e5caa4db44e3aba65df09fa7c32ad
Autor:
Jian-Hong Liu, Xiu-Xiu Wei, Ang Li, Ying-Xia Cui, Xin-Yi Xia, Wei-Song Qin, Ming-Chao Zhang, Er-Zhi Gao, Jun Sun, Chun-Lin Gao, Feng-Xia Liu, Qiu-Yue Wu, Wei-Wei Li, Asan, Zhi-Hong Liu, Xiao-Jun Li
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177685 (2017)
Alport syndrome (AS) is a clinically and genetically heterogeneous, progressive nephropathy caused by mutations in COL4A3, COL4A4, and COL4A5, which encode type IV collagen. The large sizes of these genes and the absence of mutation hot spots have co
Externí odkaz:
https://doaj.org/article/5d8fd1cbfd01476ca700cca2280e75f4
Autor:
Xi-Rong Guo, Chun-Mei Shi, Guan-Zhong Zhu, Chun-Zhao Kou, Da-Ni Qin, Jin-Gai Zhu, Chun-Lin Gao, Chen-Bo Ji, Chun-Mei Zhang, Chun Zhu
Publikováno v:
International Journal of Molecular Sciences, Vol 11, Iss 12, Pp 4814-4825 (2010)
Previous studies have determined that lin-4, which was the first miRNA to be discovered, controls the timing of cell fate determination and life span in Caenorhabditis elegans. However, the mechanism of lin-4 involvement in these processes remains po
Externí odkaz:
https://doaj.org/article/71eeb7d2ba7b44deadb773229f403e83
Publikováno v:
The Cochrane Library
Cochrane Database Syst Rev
Cochrane Database Syst Rev
Authors have made no progress with this protocol in eight years. We will not be seeking an alternative author group, as the title is not one of our priority reviews
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9671220e1908fdecf76f6b1072232dd
https://doi.org/10.1002/14651858.cd008434.pub2
https://doi.org/10.1002/14651858.cd008434.pub2
Autor:
Ying-Xia Cui, Xin-Yi Xia, Xiao-Jun Li, Er-Zhi Gao, Xiu-Xiu Wei, Ang Li, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu, Chun-Lin Gao, Jian-Hong Liu, Feng-Xia Liu, Asan
Publikováno v:
Cytogenetic and Genome Research. 154:30-36
Thin basement membrane nephropathy (TBMN), autosomal dominant Alport syndrome (ADAS), and focal segmental glomerulosclerosis (FSGS) are kidney diseases that differ in clinical diagnosis, treatment, and prognosis. Nevertheless, they may result from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d06b584dbd46e4f5909deac556e342b1
https://doi.org/10.1159/000486979
https://doi.org/10.1159/000486979
Autor:
Zhi-Hong Liu, Ying-Xia Cui, Jian-Hong Liu, Asan, Xing Lv, Er-Zhi Gao, Ang Li, Feng-Xia Liu, Xiu-Xiu Wei, Chun-Lin Gao, Zheng-Kun Xia, Xin-Yi Xia, Xiao-Jun Li
Publikováno v:
Cytogenetic and Genome Research. 154:132-136
Mutations in the COL4A5 gene result in X-linked Alport syndrome, homozygous or compound heterozygous mutations in COL4A3 or COL4A4 are responsible for autosomal recessive Alport syndrome, and heterozygous mutations in COL4A3 or COL4A4 cause autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cadacf7bbaa797a42424d38e0bb5c779
https://doi.org/10.1159/000488163
https://doi.org/10.1159/000488163