Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Fu-de Zhou"'
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 Chine
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
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
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-7 (2021)
Abstract Background Multiple myeloma (MM) is a plasma-cell derived hematologic malignant disease. The malignant proliferating plasma cells secrete massive monoclonal immunoglobulins which lead to various pathologic types of renal injury. Myeloma cast
Externí odkaz:
https://doaj.org/article/1801b4e9a8ec4b6e8397552b0e01dc4c
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 1437-1445 (2021)
Objective To investigate the demographic and clinicopathological features and renal outcomes of Chinese patients with C3 glomerulonephritis in the setting of monoclonal gammopathy. Methods Patients with renal biopsy-proven C3 glomerulonephritis and d
Externí odkaz:
https://doaj.org/article/5d58aff810054a9786f798e0d2757ad5
Autor:
Zhen-Yu Li, Shuang Wang, Dan-Yang Li, Dan Liu, Su-Xia Wang, Xiao-Juan Yu, Gang Liu, Fu-De Zhou, Ming-Hui Zhao
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
ObjectivesFibrinogen A alpha-chain amyloidosis (AFib amyloidosis) is the most common form of hereditary renal amyloidosis in the United Kingdom and Europe, but has rarely been reported in Asia. In this study, we reported two AFib amyloidosis patients
Externí odkaz:
https://doaj.org/article/8ec4904f52f445a695f40fdab580c53a
Publikováno v:
Kidney Diseases, Pp 1-10 (2020)
Introduction: Long-term exposure to mercury can cause minimal change disease. However, the current understanding of mercury-associated minimal change disease (M-MCD) is inadequate. To improve the understanding of M-MCD, this study retrospectively ana
Externí odkaz:
https://doaj.org/article/f1932a3f397b4bb5b089b9d1ed50857f
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-8 (2019)
Abstract Background The commonly used methods for amyloid typing include immunofluorescence or immunohistochemistry (IHC), which sometimes may come with diagnostic pitfalls. Mass spectrometry (MS)-based proteomics has been recognized as a reliable te
Externí odkaz:
https://doaj.org/article/1770c9de680a461599d9eaf933b20a94
Autor:
Jia Zheng, Zhao Cui, Ji-cheng Lv, Hong-zhou Duan, Su-xia Wang, Jun-qing Zhang, Fu-de Zhou, Xiao-hui Guo, Ming-hui Zhao
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-5 (2019)
Abstract Background Experimental studies have demonstrated that hypersecretion of growth hormone (GH) is associated with development of glomerular sclerosis. However, clinical case of such condition is very rare. Here we presented a case of focal seg
Externí odkaz:
https://doaj.org/article/d5f6fc43072447779a8dba3f6729580e
Publikováno v:
Nefrología (English Edition), Vol 39, Iss 6, Pp 664-671 (2019)
Background: C3 glomerulonephritis is a rare, chronic disease characterized by C3c-dominant staining on renal biopsy and is caused by inherited or acquired alternative complement pathway dysregulation. Case presentation: Here, we reported a 36-year-ol
Externí odkaz:
https://doaj.org/article/635df9a6d6aa4748a42cdced53d05b2d