Jourdy Y - Search Results

1

Prospective evaluation of automatized PF4/heparin immunoassays HemosIL HIT-ab (PF4-H) for the diagnosis of heparin-induced thrombocytopenia.

Jourdy Y, Nougier C, Rugeri L, Bordet JC, Sobas F, Negrier C. Jourdy Y, et al. Int J Lab Hematol. 2015 Apr;37(2):244-52. doi: 10.1111/ijlh.12275. Epub 2014 Jul 15. Int J Lab Hematol. 2015. PMID: 25041633

2

Comparison of an automated chemiluminescent assay to a manual ELISA assay for determination of von Willebrand Factor collagen binding activity on VWD plasma patients previously diagnosed through molecular analysis of VWF.

Jousselme E, Jourdy Y, Rugeri L, Négrier C, Nougier C. Jousselme E, et al. Among authors: jourdy y. Int J Lab Hematol. 2018 Feb;40(1):77-83. doi: 10.1111/ijlh.12743. Epub 2017 Oct 5. Int J Lab Hematol. 2018. PMID: 28980759

3

The potential value of thrombin generation assay in the diagnosis of FV inhibitors.

Désage S, Jousselme E, Le Quellec S, Lienhart A, Nougier C, Dargaud Y, Jourdy Y. Désage S, et al. Among authors: jourdy y. Int J Lab Hematol. 2019 Oct;41(5):e117-e120. doi: 10.1111/ijlh.13027. Epub 2019 Apr 6. Int J Lab Hematol. 2019. PMID: 30953579 No abstract available.

4

Single-center determination of reference factor II and factor X activity level values for the monitoring of vitamin K antagonist therapy.

Désage S, Jousselme E, Négrier C, Nougier C, Le Quellec S, Jourdy Y. Désage S, et al. Among authors: jourdy y. Int J Lab Hematol. 2019 Oct;41(5):e121-e123. doi: 10.1111/ijlh.13033. Epub 2019 Apr 23. Int J Lab Hematol. 2019. PMID: 31012536 No abstract available.

5

Characterization of five associations of F8 missense mutations containing FVIII B domain mutations.

Jourdy Y, Nougier C, Roualdes O, Fretigny M, Durand B, Negrier C, Vinciguerra C. Jourdy Y, et al. Haemophilia. 2016 Jul;22(4):583-9. doi: 10.1111/hae.12906. Epub 2016 Feb 25. Haemophilia. 2016. PMID: 26915717

6

Why patients with THBD c.1611C>A (p.Cys537X) nonsense mutation have high levels of soluble thrombomodulin?

Jourdy Y, Enjolras N, Le Quellec S, Bordet JC, Négrier C, Vinciguerra C, Dargaud Y. Jourdy Y, et al. PLoS One. 2017 Nov 16;12(11):e0188213. doi: 10.1371/journal.pone.0188213. eCollection 2017. PLoS One. 2017. PMID: 29145514 Free PMC article.

7

Splicing analysis of 26 F8 nucleotide variations using a minigene assay.

Jourdy Y, Fretigny M, Nougier C, Négrier C, Bozon D, Vinciguerra C. Jourdy Y, et al. Haemophilia. 2019 Mar;25(2):306-315. doi: 10.1111/hae.13687. Epub 2019 Jan 28. Haemophilia. 2019. PMID: 30690819

8

Molecular cytogenetic characterization of five F8 complex rearrangements: utility for haemophilia A genetic counselling.

Jourdy Y, Chatron N, Fretigny M, Carage ML, Chambost H, Claeyssens-Donadel S, Roussel-Robert V, Negrier C, Sanlaville D, Vinciguerra C. Jourdy Y, et al. Haemophilia. 2017 Jul;23(4):e316-e323. doi: 10.1111/hae.13218. Epub 2017 May 5. Haemophilia. 2017. PMID: 28475226

9

Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.

Jourdy Y, Chatron N, Carage ML, Fretigny M, Meunier S, Zawadzki C, Gay V, Negrier C, Sanlaville D, Vinciguerra C. Jourdy Y, et al. J Thromb Haemost. 2016 Oct;14(10):1988-1993. doi: 10.1111/jth.13430. Epub 2016 Sep 17. J Thromb Haemost. 2016. PMID: 27477789 Free article.

10

Effect of five therapeutic strategies on the coagulation defect induced by the thrombomodulin c.1611C>A mutation.

Dargaud Y, Jourdy Y, Le Quellec S, Hemker CH, Lindhout T, Castoldi E, Negrier C. Dargaud Y, et al. Among authors: jourdy y. Br J Haematol. 2016 Sep;174(6):993-6. doi: 10.1111/bjh.13833. Epub 2015 Oct 30. Br J Haematol. 2016. PMID: 26517807 Free article. No abstract available.

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