-
1
-
-
0032513948
-
Syndrome du QT long congenital
-
Lupoglazoff JM, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P. Syndrome du QT long congenital. Presse Med 1998; 27: 1029-34.
-
(1998)
Presse Med
, vol.27
, pp. 1029-1034
-
-
Lupoglazoff, J.M.1
Denjoy, I.2
Neyroud, N.3
Guicheney, P.4
Casasoprana, A.5
Coumel, P.6
-
2
-
-
0025935591
-
The long QT syndrome: Prospective longitudinal study of 328 families
-
Moss AJ, Schwartz PJ, Crampton RS et al. The long QT syndrome: prospective longitudinal study of 328 families. Circulation 1991; 84: 1136-44.
-
(1991)
Circulation
, vol.84
, pp. 1136-1144
-
-
Moss, A.J.1
Schwartz, P.J.2
Crampton, R.S.3
-
3
-
-
0025847714
-
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
-
Keating M, Atkinson D, Dunn C, Timothy K, Leppert M, Vincent GM. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science 1991; 252: 704-6.
-
(1991)
Science
, vol.252
, pp. 704-706
-
-
Keating, M.1
Atkinson, D.2
Dunn, C.3
Timothy, K.4
Leppert, M.5
Vincent, G.M.6
-
4
-
-
0028101967
-
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
-
Jian C, Atkinson D, Towbin JA et al. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity. Nature Genet 1994; 8: 141-7.
-
(1994)
Nature Genet
, vol.8
, pp. 141-147
-
-
Jian, C.1
Atkinson, D.2
Towbin, J.A.3
-
5
-
-
0028819671
-
Mapping of a gene for long QT syndrome to chromosome 4q25-27
-
Schott JJ, Charpentier F, Peltier S et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. Am J Hum Genet 1995; 57: 1114-22.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1114-1122
-
-
Schott, J.J.1
Charpentier, F.2
Peltier, S.3
-
6
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang Q, Curran ME, Splawski I et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet 1996; 12: 17-23.
-
(1996)
Nature Genet
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
-
7
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 1995; 80: 795-803.
-
(1995)
Cell
, vol.80
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
8
-
-
0030723260
-
Mutations in the hminK gene cause long QT syndrome and supress Iks function
-
Splawski I, Tristani-Ferouzi M, Lehmann MH, Sanguinetti MC, Keating MT. Mutations in the hminK gene cause long QT syndrome and supress Iks function. Nature Genet 1997; 17: 338-40.
-
(1997)
Nature Genet
, vol.17
, pp. 338-340
-
-
Splawski, I.1
Tristani-Ferouzi, M.2
Lehmann, M.H.3
Sanguinetti, M.C.4
Keating, M.T.5
-
9
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
Wang Q, She J, Splawski I et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995; 80: 805-11.
-
(1995)
Cell
, vol.80
, pp. 805-811
-
-
Wang, Q.1
She, J.2
Splawski, I.3
-
10
-
-
16944362512
-
Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome
-
Tanaka T, Nagai R, Tomoike H, et al. Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation. 1997; 95: 565-7.
-
(1997)
Circulation
, vol.95
, pp. 565-567
-
-
Tanaka, T.1
Nagai, R.2
Tomoike, H.3
-
11
-
-
19244371485
-
KvLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome
-
Donger C, Denjoy I, Berthet M et al. KvLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. Circulation 1997; 96: 2778-81.
-
(1997)
Circulation
, vol.96
, pp. 2778-2781
-
-
Donger, C.1
Denjoy, I.2
Berthet, M.3
-
12
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
-
Neyroud N, Tesson F, Denjoy I et al. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genet 1997; 15: 186-9.
-
(1997)
Nature Genet
, vol.15
, pp. 186-189
-
-
Neyroud, N.1
Tesson, F.2
Denjoy, I.3
-
13
-
-
6844260553
-
Intervalle QT et médicaments: Recommandations pour la prescription des médicaments chez les patients atteints du syndrome du QT long congénital
-
Le Heuzey JY, Davy JM, Weissenburger J et al. Intervalle QT et médicaments: recommandations pour la prescription des médicaments chez les patients atteints du syndrome du QT long congénital. Arch Mal Cœur 1998; 91: 59-66.
-
(1998)
Arch Mal Cœur
, vol.91
, pp. 59-66
-
-
Le Heuzey, J.Y.1
Davy, J.M.2
Weissenburger, J.3
-
14
-
-
0028786001
-
Risk of cardiac events in family members of patients with long QT syndromes
-
Zareba W, Moss AJ, Le Cessie S et al. Risk of cardiac events in family members of patients with long QT syndromes. J Am Coll Cardiol 1995; 26: 1685-91.
-
(1995)
J Am Coll Cardiol
, vol.26
, pp. 1685-1691
-
-
Zareba, W.1
Moss, A.J.2
Le Cessie, S.3
-
15
-
-
0029847602
-
Multiple mechanisms in the long QT syndrome. Current knowledge, gaps, and future directions
-
Roden DM, Lazzara R, Rosen M, Schwartz P, Towbin J, Vincent GM. Multiple mechanisms in the long QT syndrome. Current knowledge, gaps, and future directions. Circulation 1996; 94: 1996-2012.
-
(1996)
Circulation
, vol.94
, pp. 1996-2012
-
-
Roden, D.M.1
Lazzara, R.2
Rosen, M.3
Schwartz, P.4
Towbin, J.5
Vincent, G.M.6
-
16
-
-
0030981050
-
Molecular genetics of long QT syndrome from genes to patients
-
Wang Q, Chen Q, Li H, Towbin JA. Molecular genetics of long QT syndrome from genes to patients. Curr Opin Cardiol 1997; 12:310-20.
-
(1997)
Curr Opin Cardiol
, vol.12
, pp. 310-320
-
-
Wang, Q.1
Chen, Q.2
Li, H.3
Towbin, J.A.4
-
17
-
-
0031589944
-
Ion channels. Basic science and clinical disease
-
Aekerman MJ, Claphan DE. Ion channels. Basic science and clinical disease. N Engl J Med 1997; 22: 1575-86.
-
(1997)
N Engl J Med
, vol.22
, pp. 1575-1586
-
-
Aekerman, M.J.1
Claphan, D.E.2
-
18
-
-
0028618290
-
Evidence of genetic heterogeneity in Romano-Ward Long QT syndrome: Analysis of 23 families
-
Towbin JA, Li H, Taggart RT et al. Evidence of genetic heterogeneity in Romano-Ward Long QT syndrome: analysis of 23 families. Circulation 1994; 90: 2635-44.
-
(1994)
Circulation
, vol.90
, pp. 2635-2644
-
-
Towbin, J.A.1
Li, H.2
Taggart, R.T.3
-
19
-
-
0029143899
-
Readjusting the localization of long QT syndrome gene on chromosome 11p15
-
Dausse E, Denjoy I, Kahlem P et al. Readjusting the localization of long QT syndrome gene on chromosome 11p15. CR Acad Sci (III) 1995; 318: 879-85.
-
(1995)
CR Acad Sci (III)
, vol.318
, pp. 879-885
-
-
Dausse, E.1
Denjoy, I.2
Kahlem, P.3
-
21
-
-
0029002969
-
Mechanistic link between an herited and acquired cardiac arrhythmia: HERG encodes the Ikr potassium channel
-
Sanguinetti MC, Jiang C, Curran ME, Keating MT. Mechanistic link between an herited and acquired cardiac arrhythmia: HERG encodes the Ikr potassium channel. Cell 1995; 81: 299-307.
-
(1995)
Cell
, vol.81
, pp. 299-307
-
-
Sanguinetti, M.C.1
Jiang, C.2
Curran, M.E.3
Keating, M.T.4
-
22
-
-
0030022457
-
Extracellular potassium modulation of drug block of Ikr: Implications for torsade de pointes and reverse use-dependence
-
Yang T, Roden DM. Extracellular potassium modulation of drug block of Ikr: implications for torsade de pointes and reverse use-dependence. Circulation 1996; 93: 407-11.
-
(1996)
Circulation
, vol.93
, pp. 407-411
-
-
Yang, T.1
Roden, D.M.2
|