Meyer D - Search Results

1

Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity.

Ferrari S, Scheiflinger F, Rieger M, Mudde G, Wolf M, Coppo P, Girma JP, Azoulay E, Brun-Buisson C, Fakhouri F, Mira JP, Oksenhendler E, Poullin P, Rondeau E, Schleinitz N, Schlemmer B, Teboul JL, Vanhille P, Vernant JP, Meyer D, Veyradier A; French Clinical and Biological Network on Adult Thrombotic Microangiopathies. Ferrari S, et al. Among authors: meyer d. Blood. 2007 Apr 1;109(7):2815-22. doi: 10.1182/blood-2006-02-006064. Blood. 2007. PMID: 17164349 Free article.

2

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: meyer d. Blood. 2001 Sep 15;98(6):1765-72. doi: 10.1182/blood.v98.6.1765. Blood. 2001. PMID: 11535510 Free article.

3

Thrombotic thrombocytopenic purpura and its diagnosis.

Veyradier A, Meyer D. Veyradier A, et al. Among authors: meyer d. J Thromb Haemost. 2005 Nov;3(11):2420-7. doi: 10.1111/j.1538-7836.2005.01350.x. Epub 2005 May 9. J Thromb Haemost. 2005. PMID: 15892859 Free article. Review. No abstract available.

4

Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children.

Loirat C, Veyradier A, Girma JP, Ribba AS, Meyer D. Loirat C, et al. Among authors: meyer d. Semin Thromb Hemost. 2006 Mar;32(2):90-7. doi: 10.1055/s-2006-939764. Semin Thromb Hemost. 2006. PMID: 16575683 Review.

5

Complete defect in vWF-cleaving protease activity associated with increased shear-induced platelet aggregation in thrombotic microangiopathy.

Ajzenberg N, Denis CV, Veyradier A, Girma JP, Meyer D, Baruch D. Ajzenberg N, et al. Among authors: meyer d. Thromb Haemost. 2002 May;87(5):808-11. Thromb Haemost. 2002. PMID: 12038781

6

Localization of a collagen-interactive domain of human von Willebrand factor between amino acid residues Gly 911 and Glu 1,365.

Kalafatis M, Takahashi Y, Girma JP, Meyer D. Kalafatis M, et al. Among authors: meyer d. Blood. 1987 Nov;70(5):1577-83. Blood. 1987. PMID: 2889486 Free article.

7

Structure-function relationship of human von Willebrand factor.

Girma JP, Meyer D, Verweij CL, Pannekoek H, Sixma JJ. Girma JP, et al. Among authors: meyer d. Blood. 1987 Sep;70(3):605-11. Blood. 1987. PMID: 3304456 Free article. Review. No abstract available.

8

The binding domain of von Willebrand factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu 512 and Lys 673.

Christophe O, Obert B, Meyer D, Girma JP. Christophe O, et al. Among authors: meyer d. Blood. 1991 Nov 1;78(9):2310-7. Blood. 1991. PMID: 1834252 Free article.

9

New variant of von Willebrand disease with defective binding to factor VIII.

Nishino M, Girma JP, Rothschild C, Fressinaud E, Meyer D. Nishino M, et al. Among authors: meyer d. Blood. 1989 Oct;74(5):1591-9. Blood. 1989. PMID: 2506947 Free article.

10

Localization of a factor VIII binding domain on a 34 kilodalton fragment of the N-terminal portion of von Willebrand factor.

Takahashi Y, Kalafatis M, Girma JP, Sewerin K, Andersson LO, Meyer D. Takahashi Y, et al. Among authors: meyer d. Blood. 1987 Nov;70(5):1679-82. Blood. 1987. PMID: 3117138 Free article.

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