Meunier S - Search Results

1

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

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

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

5

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.

6

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.

7

Efanesoctocog Alfa Prophylaxis for Patients with Severe Hemophilia A.

von Drygalski A, Chowdary P, Kulkarni R, Susen S, Konkle BA, Oldenburg J, Matino D, Klamroth R, Weyand AC, Jimenez-Yuste V, Nogami K, Poloskey S, Winding B, Willemze A, Knobe K; XTEND-1 Trial Group. von Drygalski A, et al. N Engl J Med. 2023 Jan 26;388(4):310-318. doi: 10.1056/NEJMoa2209226. N Engl J Med. 2023. PMID: 36720133 Clinical Trial.

8

Management of a child with von Willebrand disease (type 2A) and extensive burns: a case report.

Fayolle-Pivot L, Meunier S, Tissot S, Magnin C, Bertin-Maghit M, Allaouchiche B. Fayolle-Pivot L, et al. Among authors: meunier s. Burns. 2012 Feb;38(1):e1-4. doi: 10.1016/j.burns.2011.09.023. Epub 2011 Nov 25. Burns. 2012. PMID: 22119447 No abstract available.

9

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.

10

[French guidelines. Long-term prophylaxis for severe haemophilia A and B children to prevent haemophiliac arthropathy].

Meunier S, Trossaërt M, Berger C, Borel-Derlon A, Dirat G, Donadel-Claeyssens S, Assolant AD, Guérois C, Lutz P, Rafowicz A, Rothschild C, Chambost H; Groupe Prophylaxie CoMETH. Meunier S, et al. Arch Pediatr. 2009 Dec;16(12):1571-8. doi: 10.1016/j.arcped.2009.08.010. Arch Pediatr. 2009. PMID: 19960603 French.

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