Guicheney P - Search Results

1

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. Among authors: guicheney p. Circulation. 2001 Feb 27;103(8):1095-101. doi: 10.1161/01.cir.103.8.1095. Circulation. 2001. PMID: 11222472

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

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.

Donger C, Denjoy I, Berthet M, Neyroud N, Cruaud C, Bennaceur M, Chivoret G, Schwartz K, Coumel P, Guicheney P. Donger C, et al. Among authors: guicheney p. Circulation. 1997 Nov 4;96(9):2778-81. doi: 10.1161/01.cir.96.9.2778. Circulation. 1997. PMID: 9386136

4

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

Neyroud N, Richard P, Vignier N, Donger C, Denjoy I, Demay L, Shkolnikova M, Pesce R, Chevalier P, Hainque B, Coumel P, Schwartz K, Guicheney P. Neyroud N, et al. Among authors: guicheney p. Circ Res. 1999 Feb 19;84(3):290-7. doi: 10.1161/01.res.84.3.290. Circ Res. 1999. PMID: 10024302

5

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

Berthet M, Denjoy I, Donger C, Demay L, Hammoude H, Klug D, Schulze-Bahr E, Richard P, Funke H, Schwartz K, Coumel P, Hainque B, Guicheney P. Berthet M, et al. Among authors: guicheney p. Circulation. 1999 Mar 23;99(11):1464-70. doi: 10.1161/01.cir.99.11.1464. Circulation. 1999. PMID: 10086971

6

[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.

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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