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442 results

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Page 1
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
Dragon-Durey MA, Frémeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G, Coppo P, Herman Fridman W, Weiss L. Dragon-Durey MA, et al. Among authors: blouin j. J Am Soc Nephrol. 2004 Mar;15(3):787-95. doi: 10.1097/01.asn.0000115702.28859.a7. J Am Soc Nephrol. 2004. PMID: 14978182
Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome.
Fakhouri F, Jablonski M, Lepercq J, Blouin J, Benachi A, Hourmant M, Pirson Y, Dürrbach A, Grünfeld JP, Knebelmann B, Frémeaux-Bacchi V. Fakhouri F, et al. Among authors: blouin j. Blood. 2008 Dec 1;112(12):4542-5. doi: 10.1182/blood-2008-03-144691. Epub 2008 Jul 24. Blood. 2008. PMID: 18658028 Free article.
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.
Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J, Vigneau C, Kuypers D, Boudailliez B, Loirat C, Rondeau E, Fridman WH. Fremeaux-Bacchi V, et al. Among authors: blouin j. J Med Genet. 2004 Jun;41(6):e84. doi: 10.1136/jmg.2004.019083. J Med Genet. 2004. PMID: 15173250 Free PMC article. No abstract available.
[Investigation of the complement system in clinical practice].
Frémeaux-Bacchi V, Dragon-Durey MA, Blouin J, Mouthon L, Fridman WH. Frémeaux-Bacchi V, et al. Among authors: blouin j. Ann Med Interne (Paris). 2003 Dec;154(8):529-40. Ann Med Interne (Paris). 2003. PMID: 15037829 Review. French.
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.
Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, Arzouk N, Cleper R, Francois M, Guest G, Pourrat J, Seligman R, Fridman WH, Loirat C, Atkinson JP. Fremeaux-Bacchi V, et al. Among authors: blouin j. J Am Soc Nephrol. 2006 Jul;17(7):2017-25. doi: 10.1681/ASN.2005101051. Epub 2006 Jun 8. J Am Soc Nephrol. 2006. PMID: 16762990
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome.
Frémeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, Moghal N, Kaplan BS, Weiss RA, Lhotta K, Kapur G, Mattoo T, Nivet H, Wong W, Gie S, Hurault de Ligny B, Fischbach M, Gupta R, Hauhart R, Meunier V, Loirat C, Dragon-Durey MA, Fridman WH, Janssen BJ, Goodship TH, Atkinson JP. Frémeaux-Bacchi V, et al. Among authors: blouin j. Blood. 2008 Dec 15;112(13):4948-52. doi: 10.1182/blood-2008-01-133702. Epub 2008 Sep 16. Blood. 2008. PMID: 18796626 Free PMC article.
442 results