Girma JP - Search Results

1

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Veyradier A, Lavergne JM, Ribba AS, Obert B, Loirat C, Meyer D, Girma JP. Veyradier A, et al. Among authors: girma jp. J Thromb Haemost. 2004 Mar;2(3):424-9. doi: 10.1111/j.1538-7933.2004.00623.x. J Thromb Haemost. 2004. PMID: 15009458 Free article.

2

Functional analysis of the Arg91Gln substitution in the factor VIII binding domain of von Willebrand factor demonstrates variable phenotypic expression.

Lavergne JM, Piao Y, Ribba AS, Girma JP, Siguret V, Piétu G, Boyer-Neumann C, Schandelong A, Bahnak BR, Meyer D. Lavergne JM, et al. Among authors: girma jp. Thromb Haemost. 1993 Oct 18;70(4):691-6. Thromb Haemost. 1993. PMID: 8115998

3

Structure-function relationship of the A1 domain of von Willebrand factor.

Girma JP, Ribba AS, Meyer D. Girma JP, et al. Thromb Haemost. 1995 Jul;74(1):156-60. Thromb Haemost. 1995. PMID: 8578449

4

Abnormal proteolytic processing of von Willebrand factor Arg611 Cys and Arg611His.

Nishikubo T, Christophe O, Lavergne JM, Obert B, Nonami K, Takahashi Y, Yoshioka A, Meyer D, Girma JP. Nishikubo T, et al. Among authors: girma jp. Thromb Haemost. 1997 Jan;77(1):174-82. Thromb Haemost. 1997. PMID: 9031470

5

New assay for measuring binding of platelet glycoprotein IIb/IIIa to unpurified von Willebrand factor.

Veyradier A, Jumilly AL, Ribba AS, Obert B, Houllier A, Meyer D, Girma JP. Veyradier A, et al. Among authors: girma jp. Thromb Haemost. 1999 Jul;82(1):134-9. Thromb Haemost. 1999. PMID: 10456467

6

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF.

Obert B, Tout H, Veyradier A, Fressinaud E, Meyer D, Girma JP. Obert B, et al. Among authors: girma jp. Thromb Haemost. 1999 Nov;82(5):1382-5. Thromb Haemost. 1999. PMID: 10595622

7

Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases.

Veyradier A, Obert B, Houllier A, Meyer D, Girma JP. Veyradier A, et al. Among authors: girma jp. Blood. 2001 Sep 15;98(6):1765-72. doi: 10.1182/blood.v98.6.1765. Blood. 2001. PMID: 11535510 Free article.

8

Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen.

Ribba AS, Loisel I, Lavergne JM, Juhan-Vague I, Obert B, Cherel G, Meyer D, Girma JP. Ribba AS, et al. Among authors: girma jp. Thromb Haemost. 2001 Sep;86(3):848-54. Thromb Haemost. 2001. PMID: 11583318

9

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion.

Hommais A, Stépanian A, Fressinaud E, Mazurier C, Meyer D, Girma JP, Ribba AS. Hommais A, et al. Among authors: girma jp. J Thromb Haemost. 2006 Jan;4(1):148-57. doi: 10.1111/j.1538-7836.2005.01652.x. J Thromb Haemost. 2006. PMID: 16409464 Free article.

10

Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13.

Rayes J, Hommais A, Legendre P, Tout H, Veyradier A, Obert B, Ribba AS, Girma JP. Rayes J, et al. Among authors: girma jp. J Thromb Haemost. 2007 Feb;5(2):321-8. doi: 10.1111/j.1538-7836.2007.02296.x. Epub 2006 Nov 1. J Thromb Haemost. 2007. PMID: 17087728 Free article.

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