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ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families.
Nichols WC, Terry VH, Wheatley MA, Yang A, Zivelin A, Ciavarella N, Stefanile C, Matsushita T, Saito H, de Bosch NB, Ruiz-Saez A, Torres A, Thompson AR, Feinstein DI, White GC, Negrier C, Vinciguerra C, Aktan M, Kaufman RJ, Ginsburg D, Seligsohn U. Nichols WC, et al. Among authors: negrier c. Blood. 1999 Apr 1;93(7):2261-6. Blood. 1999. PMID: 10090935 Free article.
Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development.
d'Oiron R, Lavergne JM, Lavend'homme R, Benhida A, Bordet JC, Negrier C, Peerlinck K, Vermylen J, Saint-Remy JM, Jacquemin M. d'Oiron R, et al. Among authors: negrier c. Blood. 2004 Jan 1;103(1):155-7. doi: 10.1182/blood-2003-04-1321. Epub 2003 Sep 11. Blood. 2004. PMID: 12969981 Free article.
Monitoring the bioavailability of FEIBA with a thrombin generation assay.
Váradi K, Negrier C, Berntorp E, Astermark J, Bordet JC, Morfini M, Linari S, Schwarz HP, Turecek PL. Váradi K, et al. Among authors: negrier c. J Thromb Haemost. 2003 Nov;1(11):2374-80. doi: 10.1046/j.1538-7836.2003.00450.x. J Thromb Haemost. 2003. PMID: 14629472 Free article.
The safety and efficacy of recombinant human blood coagulation factor IX in previously untreated patients with severe or moderately severe hemophilia B.
Shapiro AD, Di Paola J, Cohen A, Pasi KJ, Heisel MA, Blanchette VS, Abshire TC, Hoots WK, Lusher JM, Negrier C, Rothschild C, Roth DA. Shapiro AD, et al. Among authors: negrier c. Blood. 2005 Jan 15;105(2):518-25. doi: 10.1182/blood-2004-06-2283. Epub 2004 Sep 21. Blood. 2005. PMID: 15383463 Free article. Clinical Trial.
287 results