Bura A - Search Results

1

The incidence of venous thromboembolism in asymptomatic carriers of a deficiency of antithrombin, protein C, or protein S: a prospective cohort study.

Sanson BJ, Simioni P, Tormene D, Moia M, Friederich PW, Huisman MV, Prandoni P, Bura A, Rejto L, Wells P, Mannucci PM, Girolami A, Büller HR, Prins MH. Sanson BJ, et al. Among authors: bura a. Blood. 1999 Dec 1;94(11):3702-6. Blood. 1999. PMID: 10572082 Free article.

2

Subcutaneous heparin compared with continuous intravenous heparin administration in the initial treatment of deep vein thrombosis. A meta-analysis.

Hommes DW, Bura A, Mazzolai L, Büller HR, ten Cate JW. Hommes DW, et al. Among authors: bura a. Ann Intern Med. 1992 Feb 15;116(4):279-84. doi: 10.7326/0003-4819-116-4-279. Ann Intern Med. 1992. PMID: 1531108

3

Incidence and prognosis of cancer associated with bilateral venous thrombosis: a prospective study of 103 patients.

Bura A, Cailleux N, Bienvenu B, Léger P, Bissery A, Boccalon H, Fiessinger JN, Levesque H, Emmerich J. Bura A, et al. J Thromb Haemost. 2004 Mar;2(3):441-4. doi: 10.1111/j.1538-7933.2004.00619.x. J Thromb Haemost. 2004. PMID: 15009461 Free article.

4

A novel nonsense mutation in the antithrombin III gene (Cys-4-->stop) causing recurrent venous thrombosis.

Saleun S, De Moerloose P, Bura A, Aiach M, Emmerich J. Saleun S, et al. Among authors: bura a. Blood Coagul Fibrinolysis. 1996 Jul;7(5):578-9. doi: 10.1097/00001721-199607000-00010. Blood Coagul Fibrinolysis. 1996. PMID: 8874869

5

Homozygous variant of antithrombin with lack of affinity for heparin: management of severe thrombotic complications associated with intrauterine fetal demise.

Bauters A, Zawadzki C, Bura A, Théry C, Watel A, Subtil D, Aiach M, Emmerich J, Jude B. Bauters A, et al. Among authors: bura a. Blood Coagul Fibrinolysis. 1996 Oct;7(7):705-10. doi: 10.1097/00001721-199610000-00008. Blood Coagul Fibrinolysis. 1996. PMID: 8958394

6

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene.

Picard V, Bura A, Emmerich J, Alhenc-Gelas M, Biron C, Houbouyan-Reveillard LL, Molho P, Labatide-Alanore A, Sié P, Toulon P, Verdy E, Aiach M. Picard V, et al. Among authors: bura a. Br J Haematol. 2000 Sep;110(3):731-4. doi: 10.1046/j.1365-2141.2000.02245.x. Br J Haematol. 2000. PMID: 10997988 Free article.

7

Initial treatment of venous thromboembolism.

Becattini C, Agnelli G, Emmerich J, Bura A, Weitz JI. Becattini C, et al. Among authors: bura a. Thromb Haemost. 2006 Sep;96(3):242-50. doi: 10.1160/TH06-05-0260. Thromb Haemost. 2006. PMID: 16953263 Review.

8

[Thrombophilia and pregnancy: which tests for which patients? The clinician's point of view].

Emmerich J, Bura A. Emmerich J, et al. Among authors: bura a. Ann Med Interne (Paris). 2003 Sep-Oct;154(5-6):345-53. Ann Med Interne (Paris). 2003. PMID: 15027589 Review. French.

9

Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects.

Hulot JS, Bura A, Villard E, Azizi M, Remones V, Goyenvalle C, Aiach M, Lechat P, Gaussem P. Hulot JS, et al. Among authors: bura a. Blood. 2006 Oct 1;108(7):2244-7. doi: 10.1182/blood-2006-04-013052. Epub 2006 Jun 13. Blood. 2006. PMID: 16772608 Free article.

10

Role of the P2Y12 gene polymorphism in platelet responsiveness to clopidogrel in healthy subjects.

Bura A, Bachelot-Loza C, Ali FD, Aiach M, Gaussem P. Bura A, et al. J Thromb Haemost. 2006 Sep;4(9):2096-7. doi: 10.1111/j.1538-7836.2006.02113.x. J Thromb Haemost. 2006. PMID: 16961627 Free article. No abstract available.

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