Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Xiao-Juan Yu"'
Publikováno v:
Renal Failure, Vol 46, Iss 1 (2024)
Objective Lipoprotein glomerulopathy (LPG) is a rare disorder characterized by the development of glomerular lipoprotein thrombosis. LPG exhibits familial aggregation, with mutations in the apolipoprotein E (APOE) gene identified as the leading cause
Externí odkaz:
https://doaj.org/article/b011ecc95529495e9e7755e64be6ec24
Publikováno v:
Renal Failure, Vol 46, Iss 1 (2024)
Background Light-chain proximal tubulopathy (LCPT) is a rare disease characterized by the accumulation of monoclonal light chains within proximal tubular cells. This study aimed to investigate the clinical characteristics of LCPT from a single Chines
Externí odkaz:
https://doaj.org/article/66242db2c97049ccb428c4085ef9eee1
Autor:
Yan-jiao Cheng, Xiao-yu Jia, Hong-ru Cao, Xiao-yi Zhao, Xu-jie Zhou, Xiao-juan Yu, Rong Xu, Fu-de Zhou, Su-xia Wang, Zhao Cui, Ming-hui Zhao
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-5 (2023)
Abstract Background The phospholipase A2 receptor (PLA2R) associated with membranous nephropathy (MN) is an organ-specific autoimmune disease associated with PLA2R and human leukocyte antigen (HLA) genes. Familial PLA2R-related MN is rarely reported.
Externí odkaz:
https://doaj.org/article/3d9324bf78c9475988e8509ca9f1b9de
Autor:
Fei-Fei Chen, Xiao-Juan Yu, Hui Wang, Xu Zhang, Ying Tan, Zhen Qu, Su-Xia Wang, Feng Yu, Min Chen, Ming-Hui Zhao
Publikováno v:
Renal Failure, Vol 45, Iss 1 (2023)
AbstractObjectives This study was initiated to establish a renal thrombotic microangiopathy (TMA) scoring system based on clinical needs and investigate its predictive value for patients’ long-term outcomes.Methods Kidney biopsy-proven Complement-m
Externí odkaz:
https://doaj.org/article/64ffef51917c4aac936c79f5e941cab2
Autor:
Rui-Xue Wang, Jin-Wei Wang, Zhi-Ying Li, Su-Fang Chen, Xiao-Juan Yu, Su-Xia Wang, Fan Zhang, Zu-Ying Xiong, Shu-Hong Bi, Yue Wang, Ming-Hui Zhao, Min Chen
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-11 (2023)
Abstract Background The renal risk score (RRS) is a useful tool to predict end-stage renal disease (ESRD) in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). The current study aimed to validate the predictive perf
Externí odkaz:
https://doaj.org/article/d669bc36786a46f08015cc7649424633
Publikováno v:
Renal Failure, Vol 44, Iss 1, Pp 1123-1129 (2022)
Background Anti-glomerular basement membrane (anti-GBM) disease is a rare but severe autoantibody-mediated immune disorder. The typical clinical presentation includes rapidly progressive glomerulonephritis and often concurrent pulmonary hemorrhage. T
Externí odkaz:
https://doaj.org/article/ddaa00b0ff9a46d897819910d610e3f5
Publikováno v:
Journal of Diabetes, Vol 14, Iss 4, Pp 291-297 (2022)
Abstract Background Although extensive efforts have been paid to identify reliable predictors for renal outcomes of diabetic kidney disease (DKD) patients in type 2 diabetes mellitus (T2DM), there are still only a limited number of predictive factors
Externí odkaz:
https://doaj.org/article/e76babc954d647fda9a69f7e81d9e1c8
Publikováno v:
Kidney Diseases, Vol 8, Iss 3, Pp 249-259 (2022)
Background: Cryoglobulinemic glomerulonephritis (Cryo-GN), caused by circulating cryoglobulins, has varied etiology and clinical-pathologic manifestations. This study aimed to investigate the clinicopathological spectrum and outcome of patients with
Externí odkaz:
https://doaj.org/article/392f8d312162434c99a637637eb8fe22
Autor:
Meng-shi Li, Yang Li, Lei Jiang, Zhuo-ran Song, Xiao-juan Yu, Hui Wang, Ya-li Ren, Su-xia Wang, Xu-jie Zhou, Li Yang, Hong Zhang
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Autosomal dominant tubulointerstitial kidney disease due to UMOD mutations (ADTKD-UMOD) is a rare condition associated with high variability in the age of end-stage kidney disease (ESKD). An autosomal dominant inheritance is the general rule, but de
Externí odkaz:
https://doaj.org/article/3e87fb318a344f21a2c00420ba34e0af
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Leukocyte chemotactic factor 2-associated (ALECT2) amyloidosis is one of the recently reported types of amyloidosis, which is caused by the extracellular deposition of leukocyte chemotactic factor 2 (LECT2). There have not been any reports involving
Externí odkaz:
https://doaj.org/article/751499b139ed4862bb3118313f985c05