Lupoglazoff JM - Search Results

1

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P. Lupoglazoff JM, et al. J Am Coll Cardiol. 2004 Mar 3;43(5):826-30. doi: 10.1016/j.jacc.2003.09.049. J Am Coll Cardiol. 2004. PMID: 14998624 Free article.

2

Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.

Lupoglazoff JM, Denjoy I, Berthet M, Neyroud N, Demay L, Richard P, Hainque B, Vaksmann G, Klug D, Leenhardt A, Maillard G, Coumel P, Guicheney P. Lupoglazoff JM, et al. Circulation. 2001 Feb 27;103(8):1095-101. doi: 10.1161/01.cir.103.8.1095. Circulation. 2001. PMID: 11222472

3

[Congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Arch Pediatr. 2001 May;8(5):525-34. doi: 10.1016/s0929-693x(00)00261-x. Arch Pediatr. 2001. PMID: 11396115 Review. French.

4

[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block].

Lupoglazoff JM, Denjoy I, Cheav T, Berthet M, Extramiana F, Cauchemez B, Villain E, Leenhardt A, Guicheney P. Lupoglazoff JM, et al. Arch Mal Coeur Vaiss. 2002 May;95(5):440-6. Arch Mal Coeur Vaiss. 2002. PMID: 12085742 French.

5

[Value of genetic testing in the management of the congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Guicheney P. Lupoglazoff JM, et al. Arch Mal Coeur Vaiss. 2003 May;96(5):539-47. Arch Mal Coeur Vaiss. 2003. PMID: 12838849 Review. French.

6

[Neonatal forms of congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Legall-Petit I, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P. Lupoglazoff JM, et al. Arch Mal Coeur Vaiss. 2004 May;97(5):479-83. Arch Mal Coeur Vaiss. 2004. PMID: 15214551 French.

7

Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome.

Villain E, Denjoy I, Lupoglazoff JM, Guicheney P, Hainque B, Lucet V, Bonnet D. Villain E, et al. Among authors: lupoglazoff jm. Eur Heart J. 2004 Aug;25(16):1405-11. doi: 10.1016/j.ehj.2004.06.016. Eur Heart J. 2004. PMID: 15321698 Clinical Trial.

8

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Bartos DC, Duchatelet S, Burgess DE, Klug D, Denjoy I, Peat R, Lupoglazoff JM, Fressart V, Berthet M, Ackerman MJ, January CT, Guicheney P, Delisle BP. Bartos DC, et al. Among authors: lupoglazoff jm. Heart Rhythm. 2011 Jan;8(1):48-55. doi: 10.1016/j.hrthm.2010.09.010. Epub 2010 Sep 17. Heart Rhythm. 2011. PMID: 20850564 Free PMC article.

9

[Congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Presse Med. 1998 Jun 13;27(21):1029-34. Presse Med. 1998. PMID: 9767826 Review. French.

10

[Congenital long QT syndrome. The value of genetics in prognostic evaluation].

Denjoy I, Lupoglazoff JM, Donger C, Berthet M, Richard P, Neyroud N, Villain E, Lucet V, Coumel P, Guicheney P. Denjoy I, et al. Among authors: lupoglazoff jm. Arch Mal Coeur Vaiss. 1999 May;92(5):557-63. Arch Mal Coeur Vaiss. 1999. PMID: 10367071 French.

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