Sigaud M - Search Results

1

Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience.

Ardillon L, Ternisien C, Fouassier M, Sigaud M, Lefrançois A, Pacault M, Ribeyrol O, Fressinaud E, Boisseau P, Trossaërt M. Ardillon L, et al. Among authors: sigaud m. Haemophilia. 2015 Sep;21(5):646-52. doi: 10.1111/hae.12653. Epub 2015 Mar 10. Haemophilia. 2015. PMID: 25753785

2

A new automated method for von Willebrand factor antigen measurement using latex particles.

Veyradier A, Fressinaud E, Sigaud M, Wolf M, Meyer D. Veyradier A, et al. Among authors: sigaud m. Thromb Haemost. 1999 Feb;81(2):320-1. Thromb Haemost. 1999. PMID: 10064018 No abstract available.

3

[Evaluation of a new automated method for von Willebrand factor antigen measurement: the STA-Liatest vWF].

Veyradier A, Fressinaud E, Sigaud M, Wolf M, Meyer D. Veyradier A, et al. Among authors: sigaud m. Ann Biol Clin (Paris). 1999 May;57(3):364-8. Ann Biol Clin (Paris). 1999. PMID: 10377492 Free article. French. No abstract available.

4

Therapeutic monitoring of von Willebrand disease: interest and limits of a platelet function analyser at high shear rates.

Fressinaud E, Veyradier A, Sigaud M, Boyer-Neumann C, Le Boterff C, Meyer D. Fressinaud E, et al. Among authors: sigaud m. Br J Haematol. 1999 Sep;106(3):777-83. doi: 10.1046/j.1365-2141.1999.01604.x. Br J Haematol. 1999. PMID: 10468873 Free article.

5

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: sigaud 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.

6

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: sigaud 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

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. Among authors: sigaud m. 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. Among authors: sigaud m. 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

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. Among authors: sigaud m. 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.

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: sigaud 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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