Guicheney P - Search Results

1

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

2

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. Among authors: guicheney p. 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.

3

[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome].

Le Heuzey JY, Davy JM, Weissenburger J, Guicheney P, Le Marec H, Chevalier P, Denjoy I, Leenhardt A, Charpentier F, Coumel P. Le Heuzey JY, et al. Among authors: guicheney p. Arch Mal Coeur Vaiss. 1998 Jan;91(1):59-66. Arch Mal Coeur Vaiss. 1998. PMID: 9749265 Review. French.

4

[Congenital long QT syndrome].

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

5

[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: guicheney p. Arch Mal Coeur Vaiss. 1999 May;92(5):557-63. Arch Mal Coeur Vaiss. 1999. PMID: 10367071 French.

6

[Present concepts of congenital long QT syndrome].

Leenhardt A, Denjoy I, Maison-Blanche P, Guicheney P, Coumel P. Leenhardt A, et al. Among authors: guicheney p. Arch Mal Coeur Vaiss. 2000 Apr;93(3 Spec No):17-21. Arch Mal Coeur Vaiss. 2000. PMID: 10816797 Review. French.

7

[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].

Lupoglazoff JM, Denjoy I, Berthet M, Hainque B, Vaksmann G, Klug D, Villain E, Lucet V, Guicheney P, Coumel P. Lupoglazoff JM, et al. Among authors: guicheney p. Arch Mal Coeur Vaiss. 2001 May;94(5):470-8. Arch Mal Coeur Vaiss. 2001. PMID: 11434015 French.

8

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P. Lupoglazoff JM, et al. Among authors: guicheney p. Circ Res. 2001 Jul 20;89(2):E16-21. doi: 10.1161/hh1401.095087. Circ Res. 2001. PMID: 11463728

9

[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. Among authors: guicheney p. Arch Mal Coeur Vaiss. 2002 May;95(5):440-6. Arch Mal Coeur Vaiss. 2002. PMID: 12085742 French.

10

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

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

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