Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Asif Sadiq Wani"'
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 79-89 (2021)
Introduction Anti-glomerular basement membrane (anti-GBM) disease is a small vessel vasculitis affecting the renal and lung capillary beds. We aim to study the clinicopathological characteristics and predictors of poor outcome of this disease in our
Externí odkaz:
https://doaj.org/article/27f2ad36bc8a4086b76949dc02dd3b22
Simultaneous tubular and glomerular involvement with cryoglobulinemia vasculitis in multiple myeloma
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 6, Pp 1470-1474 (2019)
Renal manifestations in myeloma are varied. Tubulopathic light chains cause cast nephropathy or proximal tubulopathy, usually associated with tubulointerstitial nephritis. Glomerular involvement includes amyloidosis and monoclonal immunoglobulin depo
Externí odkaz:
https://doaj.org/article/2745d21071004d2ab45d619957abbda0
Publikováno v:
Journal of Drug Delivery and Therapeutics. 12:129-132
Background: The tubulointerstitial diseases can be due to a wide variety of etologies and mechanisms which vary with age, race and geographical area. In this study we aim to study the clinicopathological spectrum of biopsy proven primary tubulointers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::167904a4e9b42d1c963fc9a6ef15d6d5
https://doi.org/10.22270/jddt.v12i1.5290
https://doi.org/10.22270/jddt.v12i1.5290
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 79-89 (2021)
Renal Failure
article-version (VoR) Version of Record
Renal Failure
article-version (VoR) Version of Record
Introduction Anti-glomerular basement membrane (anti-GBM) disease is a small vessel vasculitis affecting the renal and lung capillary beds. We aim to study the clinicopathological characteristics and predictors of poor outcome of this disease in our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea0c8e7759dbb8fa0a0a15c588324174
https://doi.org/10.1080/0886022x.2020.1854301
https://doi.org/10.1080/0886022x.2020.1854301
Publikováno v:
Pediatric Nephrology. 36:601-610
Complement component 3 glomerulopathy (C3G) is a disease with limited data in children. We aimed to compare childhood C3G cases with adults. We also studied subgroups of pediatric C3G and predictors of poor outcome. This is a 12-year retrospective, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5ea179a4bbd5b07eef6b3162e7e2deb
https://doi.org/10.1007/s00467-020-04768-0
https://doi.org/10.1007/s00467-020-04768-0
Publikováno v:
Nephron. 144:228-235
Background: Complement component 3 glomerulopathy (C3G) is a disease diagnosed based on the predominance of C3 immunostaining in glomeruli. The popular electron microscopic subtyping of C3G into dense deposit disease and C3 glomerulonephritis (GN) is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec8184f798e5342db8157958d775356
https://doi.org/10.1159/000506290
https://doi.org/10.1159/000506290
Autor:
Amit Gupta, Asif Sadiq Wani, Dharmendra Bhaduaria, Raj Kumar Sharma, Anupma Kaul, Zafirah Zahir, Narayan Prasad
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 1, Pp 289-293 (2020)
Crossmatching of prospective renal transplant donors against recipients is a mandatory component of the transplant workup, being performed for over 40 years now. Allografting patients with human leukocyte antigens which are recognized by preformed an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db7c9e52119f3c43d98b13c623290ea3
http://www.sjkdt.org/article.asp?issn=1319-2442
http://www.sjkdt.org/article.asp?issn=1319-2442
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(3)
Complement component 3 glomerulopathy (C3G) is a disease with limited data in children. We aimed to compare childhood C3G cases with adults. We also studied subgroups of pediatric C3G and predictors of poor outcome.This is a 12-year retrospective, si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af811b5c9cc72cd9c91e7258f9226fdc
https://pubmed.ncbi.nlm.nih.gov/33000324
https://pubmed.ncbi.nlm.nih.gov/33000324
Simultaneous tubular and glomerular involvement with cryoglobulinemia vasculitis in multiple myeloma
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 6, Pp 1470-1474 (2019)
Renal manifestations in myeloma are varied. Tubulopathic light chains cause cast nephropathy or proximal tubulopathy, usually associated with tubulointerstitial nephritis. Glomerular involvement includes amyloidosis and monoclonal immunoglobulin depo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c456d3c3749d3a06aadeaf6887ba8917
https://pubmed.ncbi.nlm.nih.gov/31929299
https://pubmed.ncbi.nlm.nih.gov/31929299
Publikováno v:
Indian Journal of Nephrology
Indian Journal of Nephrology, Vol 30, Iss 5, Pp 301-306 (2020)
Indian Journal of Nephrology, Vol 30, Iss 5, Pp 301-306 (2020)
Background and Aims: Full-house immunofluorescence in a kidney biopsy is a common observation in lupus nephritis (LN) and was previously used synonymously with the diagnosis of LN. Though a minority of the patients will develop features suggestive of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32edfe27e942b51b1aa5d459469f2268
https://doi.org/10.4103/ijn.ijn_91_18
https://doi.org/10.4103/ijn.ijn_91_18