Girma JP - Search Results

1

Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children.

Loirat C, Girma JP, Desconclois C, Coppo P, Veyradier A. Loirat C, et al. Among authors: girma jp. Pediatr Nephrol. 2009 Jan;24(1):19-29. doi: 10.1007/s00467-008-0863-5. Epub 2008 Jun 24. Pediatr Nephrol. 2009. PMID: 18574602 Review.

2

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome.

Veyradier A, Obert B, Haddad E, Cloarec S, Nivet H, Foulard M, Lesure F, Delattre P, Lakhdari M, Meyer D, Girma JP, Loirat C. Veyradier A, et al. Among authors: girma jp. J Pediatr. 2003 Mar;142(3):310-7. doi: 10.1067/mpd.2003.79. J Pediatr. 2003. PMID: 12640381

3

Assays of ADAMTS-13 activity.

Veyradier A, Girma JP. Veyradier A, et al. Among authors: girma jp. Semin Hematol. 2004 Jan;41(1):41-7. doi: 10.1053/j.seminhematol.2003.10.005. Semin Hematol. 2004. PMID: 14727258 Review.

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: girma jp. Semin Thromb Hemost. 2006 Mar;32(2):90-7. doi: 10.1055/s-2006-939764. Semin Thromb Hemost. 2006. PMID: 16575683 Review.

5

[Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura].

Loirat C, Sellier-Leclerc AL, Frémeaux-Bacchi V, Dragon-Durey A, Girma JP, Veyradier A. Loirat C, et al. Among authors: girma jp. Nephrol Ther. 2006 Jan;2 Suppl 2:S149-61. Nephrol Ther. 2006. PMID: 17373216 Review. French.

6

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: girma jp. Thromb Haemost. 2002 May;87(5):808-11. Thromb Haemost. 2002. PMID: 12038781

7

Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Hommais A, Rayes J, Houllier A, Obert B, Legendre P, Veyradier A, Girma JP, Ribba AS. Hommais A, et al. Among authors: girma jp. Thromb Haemost. 2007 Sep;98(3):593-9. Thromb Haemost. 2007. PMID: 17849048

8

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: girma jp. Blood. 2007 Apr 1;109(7):2815-22. doi: 10.1182/blood-2006-02-006064. Blood. 2007. PMID: 17164349 Free article.

9

Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples.

Mahdian R, Rayes J, Girma JP, Houllier A, Obert B, Meyer D, Veyradier A. Mahdian R, et al. Among authors: girma jp. Thromb Haemost. 2006 Jun;95(6):1049-51. doi: 10.1160/TH06-03-0166. Thromb Haemost. 2006. PMID: 16732393 Clinical Trial. No abstract available.

10

Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.

Hommais A, Stépanian A, Fressinaud E, Mazurier C, Pouymayou K, Meyer D, Girma JP, Ribba AS. Hommais A, et al. Among authors: girma jp. Thromb Haemost. 2006 May;95(5):776-81. Thromb Haemost. 2006. PMID: 16676067

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