Le Marec H - Search Results

1

Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study.

Baruteau AE, Fouchard S, Behaghel A, Mabo P, Villain E, Thambo JB, Marçon F, Gournay V, Rouault F, Chantepie A, Guillaumont S, Godart F, Bonnet C, Fraisse A, Schleich JM, Lusson JR, Dulac Y, Leclercq C, Daubert JC, Schott JJ, Le Marec H, Probst V. Baruteau AE, et al. Among authors: le marec h. Eur Heart J. 2012 Mar;33(5):622-9. doi: 10.1093/eurheartj/ehr347. Epub 2011 Sep 14. Eur Heart J. 2012. PMID: 21920962

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

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.

5

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.

6

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype.

Lande G, Kyndt F, Baró I, Chabannes D, Boisseau P, Pony JC, Escande D, Le Marec H. Lande G, et al. Among authors: le marec h. Eur Heart J. 2001 Mar;22(5):410-22. doi: 10.1053/euhj.2000.2292. Eur Heart J. 2001. PMID: 11207083 Clinical Trial.

7

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

8

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.

9

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.

10

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Potet F, Mabo P, Le Coq G, Probst V, Schott JJ, Airaud F, Guihard G, Daubert JC, Escande D, Le Marec H. Potet F, et al. Among authors: le coq g, le marec h. J Cardiovasc Electrophysiol. 2003 Feb;14(2):200-3. doi: 10.1046/j.1540-8167.2003.02382.x. J Cardiovasc Electrophysiol. 2003. PMID: 12693506

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