Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Wan-Zhong Zou"'
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background IgG4-related disease (IgG4-RD) often affects multiple organs and tissues, especially the kidneys, and is characterized by interstitial nephritis, obstructive nephropathy, and in rare cases glomerulopathy (including membranous neph
Externí odkaz:
https://doaj.org/article/165553b929704d1e9911e6b157db67bc
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 774-778 (2021)
Background Anti-glomerular basement membrane (anti-GBM) disease is a rare autoimmune condition responsible for rapidly progressive glomerulonephritis. This disease is usually mediated by IgG autoantibodies against the noncollagenous domain of the α3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ee8923a941272241fc963a4261b2f7
https://doi.org/10.1080/0886022x.2021.1914658
https://doi.org/10.1080/0886022x.2021.1914658
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Nephrology
BMC Nephrology
Background IgG4-related disease (IgG4-RD) often affects multiple organs and tissues, especially the kidneys, and is characterized by interstitial nephritis, obstructive nephropathy, and in rare cases glomerulopathy (including membranous nephropathy).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90c152956b6e01fca4d11e9210861d08
http://link.springer.com/article/10.1186/s12882-019-1419-6
http://link.springer.com/article/10.1186/s12882-019-1419-6
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 71(6)
Patients with both anti–glomerular basement membrane (anti-GBM) disease and Castleman disease have been rarely reported. In this study, we report 3 patients with this combination. They had immunologic features similar to patients with classic anti-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bb63ce0bc8e8b453a094430925d22b5
https://pubmed.ncbi.nlm.nih.gov/29510921
https://pubmed.ncbi.nlm.nih.gov/29510921
Autor:
Suxia Wang, Min Chen, Wan-zhong Zou, Fu-de Zhou, Ying Yao, Gang Liu, Ming-Hui Zhao, Luxia Zhang
Publikováno v:
The American Journal of the Medical Sciences. 345:18-21
Background Renal light-chain amyloidosis (AL) 1 is one of the common causes of massive proteinuria and nephrotic syndrome, especially in elderly patients. This study aimed to evaluate the sensitivity and specificity of serum and urine using immunofix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a93b2871eb67890b395f92e0216341
https://doi.org/10.1097/maj.0b013e31824e0ec5
https://doi.org/10.1097/maj.0b013e31824e0ec5
Publikováno v:
American Journal of Kidney Diseases. 60:1044-1048
Lymphoblastic lymphoma is an uncommon subtype of lymphoid neoplasm in adults. Acute kidney injury at initial presentation due to lymphoblastic lymphoma infiltration of the kidneys has rarely been described. We report a 19-year-old woman who presented
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a19b07a452a3a5ed30573e61d4b27b7
https://doi.org/10.1053/j.ajkd.2012.05.023
https://doi.org/10.1053/j.ajkd.2012.05.023
Autor:
Haiyan Wang, Xiao-mei Li, Wan-Zhong Zou, Xuan Wang, Li Yang, Liqiang Meng, Shao-Qing Cai, Tao Su
Publikováno v:
Nephrology Dialysis Transplantation. 27:292-298
Background Aristolochic acid nephropathy (AAN) is a worldwide problem and one of the common causes of chronic kidney disease (CKD) in China. Methods Three hundred patients diagnosed as AAN from 1997 to 2006 were enrolled. Medical histories of Chinese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90eb0c46ca575086c118fa62944db73d
https://doi.org/10.1093/ndt/gfr291
https://doi.org/10.1093/ndt/gfr291
Publikováno v:
Nephrology Dialysis Transplantation. 26:3993-3997
Background Nephrotic syndrome is caused by a variety of glomerulopathy. The current study investigated the renal histopathological spectrum of patients with nephrotic syndrome who received a renal biopsy in our department within the last 15 years. Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc661ddd4bd2c2af344afb2c2233e0db
https://doi.org/10.1093/ndt/gfr166
https://doi.org/10.1093/ndt/gfr166
Autor:
Suxia Wang, Gang Liu, Wan-zhong Zou, Sai-nan Zhu, Zhen Qu, Ying Tan, Ming-Hui Zhao, Li-hua Wu, Jie Ao, Xin Zheng, Cai-li Wang, Feng Yu, Jun-jie Gao, Li-hua Li, Meng-Hua Chen, Zeng-yan Li, Wen-ke Wang
Publikováno v:
Kidney International. 77(9):820-829
The 2003 International Society of Nephrology/Renal Pathology Society (ISN/RPS) system for classifying patients with lupus nephritis was based on glomerular lesions exclusively, despite the fact that lupus nephritis affects all compartments of the kid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56054360fcf1afe832d49427fc385f59
Autor:
Jicheng Lv, Wan-zhong Zou, Hong Zhang, Suxia Wang, Bo Chen, Chaoxing Huang, Haiyan Wang, L. Jiang, Gang Liu
Publikováno v:
Nephrology. 14:597-605
SUMMARY: Aim: Immunoglobulin A nephropathy (IgAN) is a common and progressive glomerulonephritis. Histological lesions of IgAN are variable and considered as a risk factor for renal outcome. Establishing a relatively concise histological semiquantita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5162d99ef510ae22a576ca57da6e4a66
https://doi.org/10.1111/j.1440-1797.2008.01083.x
https://doi.org/10.1111/j.1440-1797.2008.01083.x