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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 3
1975 2
1976 1
1977 2
1978 1
1979 5
1980 3
1981 2
1982 4
1983 10
1984 6
1985 6
1986 10
1987 4
1988 10
1989 7
1990 14
1991 9
1992 15
1993 6
1994 15
1995 15
1996 12
1997 11
1998 11
1999 12
2000 16
2001 20
2002 17
2003 23
2004 17
2005 22
2006 25
2007 28
2008 32
2009 37
2010 39
2011 39
2012 41
2013 38
2014 56
2015 46
2016 34
2017 58
2018 65
2019 46
2020 50
2021 47
2022 44
2023 35
2024 21

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980 results

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Page 1
Acute glomerulonephritis.
Sethi S, De Vriese AS, Fervenza FC. Sethi S, et al. Lancet. 2022 Apr 23;399(10335):1646-1663. doi: 10.1016/S0140-6736(22)00461-5. Lancet. 2022. PMID: 35461559 Review.
All glomerulonephritis disorders can show periods of exacerbation, but disease flairs characteristically occur in patients with IgA nephropathy or C3 glomerulopathy. The gold standard for the diagnosis of a glomerulonephritis is a kidney biopsy, with a hallmark glomerular …
All glomerulonephritis disorders can show periods of exacerbation, but disease flairs characteristically occur in patients with IgA nephropa …
C3 Glomerulopathy: Pathogenesis and Treatment.
Ahmad SB, Bomback AS. Ahmad SB, et al. Adv Chronic Kidney Dis. 2020 Mar;27(2):104-110. doi: 10.1053/j.ackd.2019.12.003. Adv Chronic Kidney Dis. 2020. PMID: 32553242 Review.
C3 glomerulopathy (C3G) is a rare set of kidney diseases with 2 patterns: C3 glomerulonephritis (C3GN) and dense deposit disease. ...Although no direct treatment is available, complement blockers are either available or in the clinical trial phase. This revie …
C3 glomerulopathy (C3G) is a rare set of kidney diseases with 2 patterns: C3 glomerulonephritis (C3GN) and dense deposit disease. ... …
Type I interferon-related kidney disorders.
Lodi L, Mastrolia MV, Bello F, Rossi GM, Angelotti ML, Crow YJ, Romagnani P, Vaglio A. Lodi L, et al. Kidney Int. 2022 Jun;101(6):1142-1159. doi: 10.1016/j.kint.2022.02.031. Epub 2022 Mar 24. Kidney Int. 2022. PMID: 35339535 Review.
All these IFN-I-related disorders can cause renal dysfunction and share pathogenic and histopathological features. Collapsing glomerulopathy, a histopathological lesion characterized by podocyte loss, collapse of the vascular tuft, and parietal epithelial cell proliferatio …
All these IFN-I-related disorders can cause renal dysfunction and share pathogenic and histopathological features. Collapsing glomerulopa …
Donor-Specific Antibodies in Kidney Transplant Recipients.
Zhang R. Zhang R. Clin J Am Soc Nephrol. 2018 Jan 6;13(1):182-192. doi: 10.2215/CJN.00700117. Epub 2017 Apr 26. Clin J Am Soc Nephrol. 2018. PMID: 28446536 Free PMC article. Review.
De novo donor-specific antibodies are associated with late acute antibody-mediated rejection, chronic antibody-mediated rejection, and transplant glomerulopathy. The pathogeneses of antibody-mediated rejection include not only complement-dependent cytotoxicity, but also co …
De novo donor-specific antibodies are associated with late acute antibody-mediated rejection, chronic antibody-mediated rejection, and trans …
Complement inhibitors for kidney disease.
Wooden B, Tarragon B, Navarro-Torres M, Bomback AS. Wooden B, et al. Nephrol Dial Transplant. 2023 Nov 8;38(Supplement_2):ii29-ii39. doi: 10.1093/ndt/gfad079. Nephrol Dial Transplant. 2023. PMID: 37218685 Review.
As we increasingly recognize the important role that complement activation across all three pathways-classical, lectin and alternative-plays in glomerular lesions both rare (e.g. C3 glomerulopathy) and common (e.g. immunoglobulin A nephropathy), we can identify avenues for …
As we increasingly recognize the important role that complement activation across all three pathways-classical, lectin and alternative-plays …
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference.
Goodship TH, Cook HT, Fakhouri F, Fervenza FC, Frémeaux-Bacchi V, Kavanagh D, Nester CM, Noris M, Pickering MC, Rodríguez de Córdoba S, Roumenina LT, Sethi S, Smith RJ; Conference Participants. Goodship TH, et al. Kidney Int. 2017 Mar;91(3):539-551. doi: 10.1016/j.kint.2016.10.005. Epub 2016 Dec 16. Kidney Int. 2017. PMID: 27989322 Free article.
In both atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G) complement plays a primary role in disease pathogenesis. Herein we report the outcome of a 2015 Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference where key issues in the …
In both atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G) complement plays a primary role in disease pathogenesis …
A Narrative Review on C3 Glomerulopathy: A Rare Renal Disease.
Schena FP, Esposito P, Rossini M. Schena FP, et al. Int J Mol Sci. 2020 Jan 14;21(2):525. doi: 10.3390/ijms21020525. Int J Mol Sci. 2020. PMID: 31947692 Free PMC article. Review.
In April 2012, a group of nephrologists organized a consensus conference in Cambridge (UK) on type II membranoproliferative glomerulonephritis and decided to use a new terminology, "C3 glomerulopathy" (C3 GP). Further knowledge on the complement system and on kidney biopsy …
In April 2012, a group of nephrologists organized a consensus conference in Cambridge (UK) on type II membranoproliferative glomerulonephrit …
Transplant glomerulopathy.
Filippone EJ, McCue PA, Farber JL. Filippone EJ, et al. Mod Pathol. 2018 Feb;31(2):235-252. doi: 10.1038/modpathol.2017.123. Epub 2017 Oct 13. Mod Pathol. 2018. PMID: 29027535 Free article. Review.
In the renal allograft, transplant glomerulopathy represents a morphologic lesion and not a specific diagnosis. ...In either case, transplant glomerulopathy is associated with reduced graft survival. This review details the morphologic features of transplant glom …
In the renal allograft, transplant glomerulopathy represents a morphologic lesion and not a specific diagnosis. ...In either case, tr …
C3 glomerulopathy.
Mehdi A, Taliercio JJ. Mehdi A, et al. Cleve Clin J Med. 2023 May 24;90(6 suppl 1):e1-e4. doi: 10.3949/ccjm.90.e-s1.01. Cleve Clin J Med. 2023. PMID: 37225259 Free article.
C3 glomerulopathy (C3G) is a rare kidney disease that causes kidney dysfunction as a result of dysregulation of the complement system alternate pathway (AP). ...
C3 glomerulopathy (C3G) is a rare kidney disease that causes kidney dysfunction as a result of dysregulation of the complement system …
Lupus Nephritis.
Wenderfer SE, Eldin KW. Wenderfer SE, et al. Pediatr Clin North Am. 2019 Feb;66(1):87-99. doi: 10.1016/j.pcl.2018.08.007. Pediatr Clin North Am. 2019. PMID: 30454753 Review.
980 results