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New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study.
Le Tourneau T, Le Scouarnec S, Cueff C, Bernstein D, Aalberts JJJ, Lecointe S, Mérot J, Bernstein JA, Oomen T, Dina C, Karakachoff M, Desal H, Al Habash O, Delling FN, Capoulade R, Suurmeijer AJH, Milan D, Norris RA, Markwald R, Aikawa E, Slaugenhaupt SA, Jeunemaitre X, Hagège A, Roussel JC, Trochu JN, Levine RA, Kyndt F, Probst V, Le Marec H, Schott JJ. Le Tourneau T, et al. Among authors: trochu jn. Eur Heart J. 2018 Apr 14;39(15):1269-1277. doi: 10.1093/eurheartj/ehx505. Eur Heart J. 2018. PMID: 29020406 Free PMC article.
Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.
Kyndt F, Schott JJ, Trochu JN, Baranger F, Herbert O, Scott V, Fressinaud E, David A, Moisan JP, Bouhour JB, Le Marec H, Bénichou B. Kyndt F, et al. Among authors: trochu jn. Am J Hum Genet. 1998 Mar;62(3):627-32. doi: 10.1086/301747. Am J Hum Genet. 1998. PMID: 9497244 Free PMC article.
Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy.
Kyndt F, Gueffet JP, Probst V, Jaafar P, Legendre A, Le Bouffant F, Toquet C, Roy E, McGregor L, Lynch SA, Newbury-Ecob R, Tran V, Young I, Trochu JN, Le Marec H, Schott JJ. Kyndt F, et al. Among authors: trochu jn. Circulation. 2007 Jan 2;115(1):40-9. doi: 10.1161/CIRCULATIONAHA.106.622621. Epub 2006 Dec 26. Circulation. 2007. PMID: 17190868
Molecular risk stratification in advanced heart failure patients.
Lamirault G, Meur NL, Roussel JC, Cunff MF, Baron D, Bihouée A, Guisle I, Raharijaona M, Ramstein G, Teusan R, Chevalier C, Gueffet JP, Trochu JN, Léger JJ, Houlgatte R, Steenman M. Lamirault G, et al. Among authors: trochu jn. J Cell Mol Med. 2010 Jun;14(6B):1443-52. doi: 10.1111/j.1582-4934.2009.00913.x. Epub 2009 Sep 30. J Cell Mol Med. 2010. PMID: 19793385 Free PMC article.
189 results