Berthet M - Search Results

1

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: berthet m. Circ Res. 2001 Jul 20;89(2):E16-21. doi: 10.1161/hh1401.095087. Circ Res. 2001. PMID: 11463728

2

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: berthet m. Circulation. 1997 Nov 4;96(9):2778-81. doi: 10.1161/01.cir.96.9.2778. Circulation. 1997. PMID: 9386136

3

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. Circulation. 1999 Mar 23;99(11):1464-70. doi: 10.1161/01.cir.99.11.1464. Circulation. 1999. PMID: 10086971

4

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

5

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: berthet m. Circulation. 2001 Feb 27;103(8):1095-101. doi: 10.1161/01.cir.103.8.1095. Circulation. 2001. PMID: 11222472

6

[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: berthet m. Arch Mal Coeur Vaiss. 2001 May;94(5):470-8. Arch Mal Coeur Vaiss. 2001. PMID: 11434015 French.

7

[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: berthet m. Arch Mal Coeur Vaiss. 2002 May;95(5):440-6. Arch Mal Coeur Vaiss. 2002. PMID: 12085742 French.

8

[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. Among authors: berthet m. Arch Mal Coeur Vaiss. 2004 May;97(5):479-83. Arch Mal Coeur Vaiss. 2004. PMID: 15214551 French.

9

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: berthet m. 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.

10

Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers.

Extramiana F, Denjoy I, Badilini F, Chabani I, Neyroud N, Berthet M, Fressard V, Guicheney P, Beaufils P, Leenhardt A, Coumel P, Maison-Blanche P. Extramiana F, et al. Among authors: berthet m. Am J Cardiol. 2005 Feb 1;95(3):406-9. doi: 10.1016/j.amjcard.2004.09.045. Am J Cardiol. 2005. PMID: 15670556

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