Déficits en protéines du complément en pathologie humaine : Déficits immunitaires primitifs de l'adulte. Un diagnostic à ne pas méconnaître = Complément component deficiencies in human diseaseDRAGON-DUREY, Marie-Agnès; FREMEAUX-BACCHI, Véronique.La Presse médicale (1983). 2006, Vol 35, Num 5, pp 861-870, issn 0755-4982, 10 p., CAH2Article

Atypical haemolytic uraemic syndrome and mutations in complement regulator genesDRAGON-DUREY, Marie-Agnès; FREMEAUX-BACCHI, Véronique.Springer seminars in immunopathology. 2005, Vol 27, Num 3, pp 359-374, issn 0344-4325, 16 p.Article

Diagnostic biologique de la maladie cœliaque : Maladie coeliaque = Serological diagnosis of celiac diseaseDE CHAISEMARTIN, Luc; FERNANI-OUKIL, Fahima; DRAGON-DUREY, Marie-Agnès et al.La Lettre de l'hépato-gastroentérologue. 2012, Vol 15, Num 6, pp 252-254, issn 1286-580X, 3 p.Article

Le complément en Médecine Interne = Investigation of the complement system in clinical practiceFREMEAUX-BACCHI, Véronique; DRAGON-DUREY, Marie-Agnès; BLOUIN, Jacques et al.Annales de médecine interne (Paris). 2003, Vol 154, Num 8, pp 529-540, issn 0003-410X, 12 p.Article

Autoantibodies in haemolytic uraemic syndrome (HUS)SKERKA, Christine; JOZSI, Mihaly; ZIPFEL, Peter F et al.Thrombosis and haemostasis. 2009, Vol 101, Num 2, pp 227-232, issn 0340-6245, 6 p.Conference Paper

Pulse Cyclophosphamide Therapy and Clinical Remission in Atypical Hemolytic Uremic Syndrome With Anti-Complement Factor H AutoantibodiesBOYER, Olivia; BALZAMO, Eve; CHARBIT, Marina et al.American journal of kidney diseases. 2010, Vol 55, Num 5, pp 923-927, issn 0272-6386, 5 p.Article

Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two casesKWON, Theresa; BELOT, Alexandre; RANCHIN, Bruno et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 9, pp 2752-2754, issn 0931-0509, 3 p.Article

Déficits en protéines du complément et pathologies humaines = Complement deficiencies and human diseasesROSAIN, Jérémiei; NGO, Stéphanie; BORDEREAU, Pauline et al.Annales de biologie clinique (Paris). 2014, Vol 72, Num 3, pp 271-280, issn 0003-3898, 10 p.Article

Unusual clinical severity of complement membrane cofactor protein-associated hemolytic-uremic syndrome and uniparental isodisomyFREMEAUX-BACCHI, Veronique; SANLAVILLE, Damien; MENOUER, Soraya et al.American journal of kidney diseases. 2007, Vol 49, Num 2, pp 323-329, issn 0272-6386, 7 p.Article

Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndromeKWON, Theresa; DRAGON-DUREY, Marie-Agnes; MACHER, Marie-Alice et al.Nephrology, dialysis, transplantation (Print). 2008, Vol 23, Num 6, pp 2088-2090, issn 0931-0509, 3 p.Article

Alternative complement pathway assessment in patients with atypical HUSROUMENINA, Lubka T; LOIRAT, Chantal; DRAGON-DUREY, Marie-Agnes et al.Journal of immunological methods. 2011, Vol 365, Num 1-2, pp 8-26, issn 0022-1759, 19 p.Article

Anti-factor H autoantibodies associated with atypical hemolytic uremic syndromeDRAGON-DUREY, Marie-Agnès; LOIRAT, Chantal; CLOAREC, Sylvie et al.Journal of the American Society of Nephrology. 2005, Vol 16, Num 2, pp 555-563, issn 1046-6673, 9 p.Article

Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 casesDRAGON-DUREY, Marie-Agnès; FREMEAUX-BACCHI, Véronique; LOIRAT, Chantal et al.Journal of the American Society of Nephrology. 2004, Vol 15, Num 3, pp 787-795, issn 1046-6673, 9 p.Article

Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene MutationsFAKHOURI, Fadi; ROUMENINA, Lubka; RONDEAU, Eric et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 5, pp 859-867, issn 1046-6673, 9 p.Article

Inhibition of the mTORC Pathway in the Antiphospholipid SyndromeCANAUD, Guillaume; BIENAIME, Frank; LEGENDRE, Christophe et al.The New England journal of medicine. 2014, Vol 371, Num 4, pp 303-312, issn 0028-4793, 10 p.Article

Anti-Factor H Autoantibody―Associated Hemolytic Uremic Syndrome: Review of Literature of the Autoimmune Form of HUSDRAGON-DUREY, Marie-Agnès; BLANC, Caroline; GARNIER, Arnaud et al.Seminars in thrombosis and hemostasis. 2010, Vol 36, Num 6, pp 633-640, issn 0094-6176, 8 p.Article

Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2FREMEAUX-BACCHI, Véronique; GUINNEPAIN, Marie-Thérèse; WEISS, Laurence et al.The American journal of medicine. 2002, Vol 113, Num 3, pp 194-199, issn 0002-9343Article

Lupus Nephritis Associated With Complete C1s Deficiency Efficiently Treated With Rituximab: A Case ReportBIENAIME, Frank; QUARTIER, Pierre; DRAGON-DUREY, Marie-Agnes et al.Arthritis care and research. 2010, Vol 62, Num 9, pp 1346-1350, issn 0893-7524, 5 p.Article

Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 DeficiencyBEOM HEE LEE; SOO HEON KWAK; HAE IL CHEONG et al.Pediatric research. 2009, Vol 66, Num 3, pp 336-340, issn 0031-3998, 5 p.Article

Heterogeneous pattern of renal disease associated with homozygous Factor H deficiencySERVAIS, Aude; NOË, Laure-Hélène; LESAVRE, Philippe et al.Human pathology. 2011, Vol 42, Num 9, pp 1305-1311, issn 0046-8177, 7 p.Article

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeFREMEAUX-BACCHI, Veronique; MILLER, Elizabeth C; KAPUR, Gaurav et al.Blood. 2008, Vol 112, Num 13, pp 4948-4952, issn 0006-4971, 5 p.Article

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndromeFREMEAUX-BACCHI, Véronique; MOULTON, Elizabeth A; POURRAT, Jacques et al.Journal of the American Society of Nephrology. 2006, Vol 17, Num 7, pp 2017-2025, issn 1046-6673, 9 p.Article

Clinical Features of Anti-Factor H Autoantibody-Associated Hemolytic Uremic SyndromeDRAGON-DUREY, Marie-Agnès; SIDHARTH KUMAR SETHI; LE QUINTREC, Moglie et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 12, pp 2180-2187, issn 1046-6673, 8 p.Article

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndromeSELLIER-LEDERC, Anne-Laure; FREMEAUX-BACCHI, Veronique; TSIMARATOS, Michel et al.Journal of the American Society of Nephrology. 2007, Vol 18, Num 8, pp 2392-2400, issn 1046-6673, 9 p.Article

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathiesSERVAIS, Aude; NOËL, Laure-Hélène; MOULIN, Bruno et al.Kidney international. 2012, Vol 82, Num 4, pp 454-464, issn 0085-2538, 11 p.Article