Meunier S - Search Results

1

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. Among authors: meunier s. 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.

2

Haemophilia and thrombophilia: an unexpected association!

Dargaud Y, Meunier S, Negrier C. Dargaud Y, et al. Among authors: meunier s. Haemophilia. 2004 Jul;10(4):319-26. doi: 10.1111/j.1365-2516.2004.00906.x. Haemophilia. 2004. PMID: 15230944 Review.

3

Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision.

Dargaud Y, Lienhart A, Meunier S, Hequet O, Chavanne H, Chamouard V, Marin S, Negrier C. Dargaud Y, et al. Among authors: meunier s. Haemophilia. 2005 Sep;11(5):552-8. doi: 10.1111/j.1365-2516.2005.01141.x. Haemophilia. 2005. PMID: 16128902

4

Adaptability of protein A-immunoadsorption allows temporary reduction of anti-VIII antibodies and realisation of high-risk haemorrhagic surgery.

Hequet O, Lienhart A, Jaeger S, Meunier S, Sobas F, Rigal D, Negrier C. Hequet O, et al. Among authors: meunier s. Transfus Apher Sci. 2007 Jun;36(3):255-8. doi: 10.1016/j.transci.2007.04.003. Epub 2007 Jun 13. Transfus Apher Sci. 2007. PMID: 17569589

5

Contribution of genetical analysis for diagnosis of von Willebrand's disease type 2B.

Victor M, Rugeri L, Nougier C, Meunier S, Fretigny M, Negrier C, Vinciguerra C. Victor M, et al. Among authors: meunier s. Haemophilia. 2009 Mar;15(2):610-2. doi: 10.1111/j.1365-2516.2008.01966.x. Epub 2009 Feb 1. Haemophilia. 2009. PMID: 19187192 No abstract available.

6

Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements.

Trossaert M, Lienhart A, Nougier C, Fretigny M, Sigaud M, Meunier S, Fouassier M, Ternisien C, Negrier C, Dargaud Y. Trossaert M, et al. Among authors: meunier s. Haemophilia. 2014 Jul;20(4):550-8. doi: 10.1111/hae.12381. Epub 2014 Feb 12. Haemophilia. 2014. PMID: 24517184

7

Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A.

Saultier P, Guillaume Y, Demiguel V, Berger C, Borel-Derlon A, Claeyssens S, Harroche A, Oudot C, Rafowicz A, Trossaert M, Wibaut B, Vinciguerra C, Boucekine M, Baumstarck K, Meunier S, Calvez T, Chambost H; FranceCoag PUPs / CoMETH Prophylaxis Study Group; Hemophilia Treatment Centers of Paris-Necker. Saultier P, et al. Among authors: meunier s. J Pediatr. 2021 Jul;234:212-219.e3. doi: 10.1016/j.jpeds.2021.02.071. Epub 2021 Mar 4. J Pediatr. 2021. PMID: 33676933 Clinical Trial.

8

Choice of factor VIII/IX regimen in adolescents and young adults with severe or moderately severe haemophilia. A French national observational study (ORTHem 15-25).

Meunier S, d'oiron R, Chambost H, Dolimier E, Guillet B; ORTHem 15-25 Study Group. Meunier S, et al. Thromb Res. 2017 Mar;151:17-22. doi: 10.1016/j.thromres.2016.12.023. Epub 2016 Dec 28. Thromb Res. 2017. PMID: 28088606 Free article.

9

Individualized PK-based prophylaxis in severe haemophilia.

Dargaud Y, Delavenne X, Hart DP, Meunier S, Mismetti P. Dargaud Y, et al. Among authors: meunier s. Haemophilia. 2018 Mar;24 Suppl 2:3-17. doi: 10.1111/hae.13397. Haemophilia. 2018. PMID: 29543364 Review.

10

Use of clinical practice guidelines on long-term prophylaxis in severe hemophilia in France: a retrospective audit.

Meunier S, Chambost H, Demiguel V, Doncarli A, Suzan F, Trossaërt M. Meunier S, et al. J Pediatr. 2013 Jun;162(6):1241-4, 1244.e1. doi: 10.1016/j.jpeds.2012.11.080. Epub 2013 Jan 17. J Pediatr. 2013. PMID: 23333129

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