Le Marec H - Search Results

1

Familial aggregation of calcific aortic valve stenosis in the western part of France.

Probst V, Le Scouarnec S, Legendre A, Jousseaume V, Jaafar P, Nguyen JM, Chaventré A, Le Marec H, Schott JJ. Probst V, et al. Among authors: le scouarnec s, le marec h. Circulation. 2006 Feb 14;113(6):856-60. doi: 10.1161/CIRCULATIONAHA.105.569467. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461814

2

[Hereditary cardiac arrhythmia].

Le Marec H, Schott JJ. Le Marec H, et al. Arch Mal Coeur Vaiss. 1997 Apr;90 Spec No 1:57-66. Arch Mal Coeur Vaiss. 1997. PMID: 9238458 Review. French.

3

[Congenital long QT syndromes].

Le Marec H, Schott JJ. Le Marec H, et al. Arch Mal Coeur Vaiss. 1997 Jun;90 Spec No 3:25-35. Arch Mal Coeur Vaiss. 1997. PMID: 9295920 French.

4

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: le marec h. Am J Hum Genet. 1998 Mar;62(3):627-32. doi: 10.1086/301747. Am J Hum Genet. 1998. PMID: 9497244 Free PMC article.

5

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Among authors: le marec h. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

6

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H. Trochu JN, et al. Among authors: le marec h. J Am Coll Cardiol. 2000 Jun;35(7):1890-7. doi: 10.1016/s0735-1097(00)00617-3. J Am Coll Cardiol. 2000. PMID: 10841240 Free article.

7

Electropharmacological characterization of cardiac repolarization in German shepherd dogs with an inherited syndrome of sudden death: abnormal response to potassium channel blockers.

Mérot J, Probst V, Debailleul M, Gerlach U, Moise NS, Le Marec H, Charpentier F. Mérot J, et al. Among authors: le marec h. J Am Coll Cardiol. 2000 Sep;36(3):939-47. doi: 10.1016/s0735-1097(00)00811-1. J Am Coll Cardiol. 2000. PMID: 10987623 Free article.

8

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Kyndt F, et al. Among authors: le marec h. Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834. Circulation. 2001. PMID: 11748104

9

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baró I, Escande D, Le Marec H. Probst V, et al. Among authors: le marec h. J Am Coll Cardiol. 2003 Feb 19;41(4):643-52. doi: 10.1016/s0735-1097(02)02864-4. J Am Coll Cardiol. 2003. PMID: 12598077 Free article.

10

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.

Probst V, Allouis M, Kyndt F, Lande G, Trochu JN, Schott JJ, Le Marec H. Probst V, et al. Among authors: le marec h. Am J Cardiol. 2003 Mar 1;91(5):635-7. doi: 10.1016/s0002-9149(02)03329-5. Am J Cardiol. 2003. PMID: 12615283 No abstract available.

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