Literature DB >> 25532781

C3 glomerulonephritis associated with complement factor B mutation.

Sanjeev Sethi1, Richard J H Smith2, John J Dillon3, Fernando C Fervenza3.   

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Year:  2014        PMID： 25532781     DOI： 10.1053/j.ajkd.2014.10.023

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN： 0272-6386            Impact factor:   8.860


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  5 in total

1.  Rare genetic variant in the CFB gene presenting as atypical hemolytic uremic syndrome and immune complex diffuse membranoproliferative glomerulonephritis, with crescents, successfully treated with eculizumab.

Authors:  Khalid Alfakeeh; Mohammed Azar; Majid Alfadhel; Alsuayri Mansour Abdullah; Nourah Aloudah; Khaled O Alsaad
Journal:  Pediatr Nephrol       Date:  2017-02-16       Impact factor: 3.714

Review 2.  Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.

Authors:  Maurizio Salvadori; Giuseppina Rosso
Journal:  World J Nephrol       Date:  2016-07-06

3.  Renal and Pulmonary Dense Deposit Disease Presenting as Pulmonary-Renal Syndrome.

Authors:  Ritambhra Nada; Ashwani Kumar; Parimal Agrawal; Raja Ramachandran; Sanjeev Sethi
Journal:  Kidney Int Rep       Date:  2018-01-31

Review 4.  C3 glomerulopathy and atypical hemolytic uremic syndrome: an updated review of the literature on alternative complement pathway disorders.

Authors:  Kultigin Turkmen; Ismail Baloglu; Hakan Ozer
Journal:  Int Urol Nephrol       Date:  2021-01-03       Impact factor: 2.370

5.  Combination of a Novel Genetic Variant in CFB Gene and a Pathogenic Variant in COL4A5 Gene in a Sibling Renal Disease: A Case Report.

Authors:  Feng-Mei Wang; Yan Yang; Xiao-Liang Zhang; Yan-Li Wang; Yan Tu; Bi-Cheng Liu; Bin Wang
Journal:  Front Genet       Date:  2021-07-19       Impact factor: 4.599
  5 in total

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