Trossaërt M - Search Results

1

Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one-stage and chromogenic factor VIII activity.

Trossaërt M, Boisseau P, Quemener A, Sigaud M, Fouassier M, Ternisien C, Lefrançois-Bettembourg A, Tesson C, Thomas C, Bezieau S. Trossaërt M, et al. J Thromb Haemost. 2011 Mar;9(3):524-30. doi: 10.1111/j.1538-7836.2010.04174.x. J Thromb Haemost. 2011. PMID: 21166991 Free article.

2

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation.

Quélin F, Trossaërt M, Sigaud M, Mazancourt PD, Fressinaud E. Quélin F, et al. Among authors: trossaert m. J Thromb Haemost. 2004 Jan;2(1):71-6. doi: 10.1111/j.1538-7836.2004.00554.x. J Thromb Haemost. 2004. PMID: 14717969 Free article.

3

Evaluation of denaturing high-performance liquid chromatography (DHPLC) in the screening of mutations in hemophilia B patients.

Herbert O, Trossaërt M, Boisseau P, Fressinaud E, Gerson F. Herbert O, et al. Among authors: trossaert m. J Thromb Haemost. 2004 Dec;2(12):2267-9. doi: 10.1111/j.1538-7836.2004.01019.x. J Thromb Haemost. 2004. PMID: 15613048 Free article. No abstract available.

4

Molecular misdiagnosis in type 2B von Willebrand disease.

Schmitt S, Trossaert M, Airaud F, Landeau-Trottier G, Talarmain P, Boisseau P, Fressinaud E, Bezieau S. Schmitt S, et al. Among authors: trossaert m. Am J Hematol. 2006 Oct;81(10):805-6. doi: 10.1002/ajh.20661. Am J Hematol. 2006. PMID: 16783788 Free article. No abstract available.

5

Iliopsoas hematoma in patients with hemophilia: a single-center study.

Dauty M, Sigaud M, Trossaërt M, Fressinaud E, Letenneur J, Dubois C. Dauty M, et al. Among authors: trossaert m. Joint Bone Spine. 2007 Mar;74(2):179-83. doi: 10.1016/j.jbspin.2006.05.014. Epub 2007 Feb 2. Joint Bone Spine. 2007. PMID: 17336570

6

Prospective evaluation of the '4Ts' score and particle gel immunoassay specific to heparin/PF4 for the diagnosis of heparin-induced thrombocytopenia.

Pouplard C, Gueret P, Fouassier M, Ternisien C, Trossaert M, Régina S, Gruel Y. Pouplard C, et al. Among authors: trossaert m. J Thromb Haemost. 2007 Jul;5(7):1373-9. doi: 10.1111/j.1538-7836.2007.02524.x. Epub 2007 Mar 14. J Thromb Haemost. 2007. PMID: 17362241 Free article.

7

Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype.

Trossaërt M, Regnault V, Sigaud M, Boisseau P, Fressinaud E, Lecompte T. Trossaërt M, et al. J Thromb Haemost. 2008 Mar;6(3):486-93. doi: 10.1111/j.1538-7836.2007.02861.x. Epub 2007 Nov 28. J Thromb Haemost. 2008. PMID: 18047548 Free article.

8

Evaluation of an automated von Willebrand factor activity assay in von Willebrand disease.

Trossaërt M, Ternisien C, Lefrancois A, Llopis L, Goudemand J, Sigaud M, Fouassier M, Caron C. Trossaërt M, et al. Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):E25-9. doi: 10.1177/1076029610379848. Epub 2010 Aug 19. Clin Appl Thromb Hemost. 2011. PMID: 20724302 Free article.

9

Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis.

Veyradier A, Caron C, Ternisien C, Wolf M, Trossaert M, Fressinaud E, Goudemand J. Veyradier A, et al. Among authors: trossaert m. Haemophilia. 2011 Nov;17(6):944-51. doi: 10.1111/j.1365-2516.2011.02499.x. Epub 2011 Mar 3. Haemophilia. 2011. PMID: 21371195

10

Acquired von Willebrand syndrome associated with monoclonal gammopathy: a single-center study of 36 patients.

Voisin S, Hamidou M, Lefrançois A, Sigaud M, Mahé B, Trossaërt M. Voisin S, et al. Among authors: trossaert m. Medicine (Baltimore). 2011 Nov;90(6):404-411. doi: 10.1097/MD.0b013e3182397166. Medicine (Baltimore). 2011. PMID: 22033454 Free article.

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