Lupoglazoff JM - Search Results

1

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.

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. 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

[Congenital long QT syndrome: an elective indication for betablocker treatment. Apropos of 5 cases].

Hayoun B, Lupoglazoff JM, Magnier S, Denjoy I, Casasoprana A. Hayoun B, et al. Among authors: lupoglazoff jm. Arch Mal Coeur Vaiss. 1995 May;88(5):737-42. Arch Mal Coeur Vaiss. 1995. PMID: 7646286 Review. French.

4

[Long QT syndrome under cisapride in neonates and infants].

Lupoglazoff JM, Bedu A, Faure C, Denjoy I, Casasoprana A, Cézard JP, Aujard Y. Lupoglazoff JM, et al. Arch Pediatr. 1997 Jun;4(6):509-14. doi: 10.1016/s0929-693x(97)87568-9. Arch Pediatr. 1997. PMID: 9239264 French.

5

[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.

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: lupoglazoff jm. 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. 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. 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. 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. Arch Mal Coeur Vaiss. 2003 May;96(5):539-47. Arch Mal Coeur Vaiss. 2003. PMID: 12838849 Review. French.

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