Different types of glomerulonephritis associated with the dysregulation of the complement alternative pathway in 2 brothers
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference18 articles.
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2. Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies;Servais;Kidney Int,2012
3. Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis;Gale;Lancet,2010
4. A hybrid CFHR3-1 gene causes familial C3 glomerulopathy;Malik;J Am Soc Nephrol,2012
5. Hemolytic uremic syndrome;Noris;J Am Soc Nephrol,2005
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1. Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritis;Frontiers in Immunology;2022-09-23
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3. Nephrotic syndrome in a 7-year-old girl with atypical hemolytic uremic syndrome relapse: Answers;Pediatric Nephrology;2020-07-14
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5. The role of the alternative pathway of complement activation in glomerular diseases;Clinical and Experimental Medicine;2018-02-15
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