Quélin F - Search Results

1

A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.

de Mazancourt P, Quélin F, Flaujac C, de Raucourt E, Guillet B, Bauduer F, Ernest V, Beurrier P, Avril A, d'Oiron R, Biron-Andréani C, Meunier S, Dargaud Y. de Mazancourt P, et al. Among authors: quelin f. Haemophilia. 2023 Jul;29(4):1113-1120. doi: 10.1111/hae.14802. Epub 2023 May 30. Haemophilia. 2023. PMID: 37252892

2

Thrombin generation in patients with factor XI deficiency and clinical bleeding risk.

Rugeri L, Quélin F, Chatard B, De Mazancourt P, Negrier C, Dargaud Y. Rugeri L, et al. Among authors: quelin f. Haemophilia. 2010 Sep 1;16(5):771-7. doi: 10.1111/j.1365-2516.2010.02246.x. Epub 2010 Apr 8. Haemophilia. 2010. PMID: 20398070

3

Four novel FXI gene mutations in three factor XI- deficient patients.

de Raucourt E, de Mazancourt P, Quélin F. de Raucourt E, et al. Among authors: quelin f. Blood Coagul Fibrinolysis. 2008 Apr;19(3):240-2. doi: 10.1097/MBC.0b013e3282f6d256. Blood Coagul Fibrinolysis. 2008. PMID: 18388506

4

Characterization of combined factor VII and factor XI deficiencies.

Quélin F, De Raucourt E, Mathonnet F, Tétégan M, Peltier JY, De Mazancourt P. Quélin F, et al. Haemophilia. 2008 May;14(3):639-42. doi: 10.1111/j.1365-2516.2007.01646.x. Epub 2008 Jan 28. Haemophilia. 2008. PMID: 18248411 No abstract available.

5

Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K).

Quélin F, François D, d'Oiron R, Guillet B, de Raucourt E, de Mazancourt P. Quélin F, et al. Haematologica. 2005 Aug;90(8):1149-50. Haematologica. 2005. PMID: 16079124

6

The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal A{alpha} disulfide bonds in protein assembly and secretion.

Hanss M, Pouymayou C, Blouch MT, Lellouche F, Ffrench P, Rousson R, Abgrall JF, Morange PE, Quélin F, de Mazancourt P. Hanss M, et al. Among authors: quelin f. Haematologica. 2011 Aug;96(8):1226-30. doi: 10.3324/haematol.2010.029801. Epub 2011 Apr 1. Haematologica. 2011. PMID: 21459789 Free PMC article.

7

Prospective analysis of factor XI deficiencies in the Marseilles area identified four novel mutations among 12 consecutive unrelated families.

Quélin F, Frère C, Pouymayou C, Morange P, de Mazancourt P, Juhan-Vague I. Quélin F, et al. Blood Coagul Fibrinolysis. 2009 Jan;20(1):84-8. doi: 10.1097/MBC.0b013e32831bc51c. Blood Coagul Fibrinolysis. 2009. PMID: 20523169

8

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.

Quélin F, Mathonnet F, Potentini-Esnault C, Trigui N, Peynet J, Bastenaire B, Guillon L, Bigel ML, Sauger A, Mazurier C, de Mazancourt P. Quélin F, et al. Blood Coagul Fibrinolysis. 2006 Jan;17(1):69-73. doi: 10.1097/01.mbc.0000198054.50257.96. Blood Coagul Fibrinolysis. 2006. PMID: 16607084

9

Fibrinogen angers with a new deletion (gamma GVYYQ 346-350) causes hypofibrinogenemia with hepatic storage.

Dib N, Quelin F, Ternisien C, Hanss M, Michalak S, De Mazancourt P, Rousselet MC, Calès P. Dib N, et al. Among authors: quelin f. J Thromb Haemost. 2007 Oct;5(10):1999-2005. doi: 10.1111/j.1538-7836.2007.02713.x. J Thromb Haemost. 2007. PMID: 17883696 Free article.

10

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. 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.

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