-
1
-
-
0001487688
-
The pathology of complete atrio-ventricular block
-
Lenegre J. The pathology of complete atrio-ventricular block. Prog Cardiovas Dis 1964;6:317-23.
-
(1964)
Prog Cardiovas Dis
, vol.6
, pp. 317-323
-
-
Lenegre, J.1
-
2
-
-
0000901789
-
Anatomic basis for atrioventricular block
-
Lev M. Anatomic basis for atrioventricular block. Am J Cardiol 1964;37:742-8.
-
(1964)
Am J Cardiol
, vol.37
, pp. 742-748
-
-
Lev, M.1
-
3
-
-
0017054549
-
Pathology of chronic AV block
-
Davies MJ. Pathology of chronic AV block. Acta Cardiol 1976;21:19-30. (Pubitemid 8000849)
-
(1976)
Acta Cardiologica
, vol.31
, Issue.SUPPL. 21
, pp. 19-30
-
-
Davies, M.J.1
-
5
-
-
0028962264
-
Gene for progressive familial heart block type i maps to chromosome 19q13
-
Brink PA, Ferreira A, Moolman JC, et al. Gene for progressive familial heart block type I maps to chromosome 19q13. Circulation 1995;91:1633-40.
-
(1995)
Circulation
, vol.91
, pp. 1633-1640
-
-
Brink, P.A.1
Ferreira, A.2
Moolman, J.C.3
-
6
-
-
0013379304
-
Congenital arrhythmias and conduction abnormalities in a father and four children
-
Segall HN. Congenital arrhythmias and conduction abnormalities in a father and four children. Can Med Assoc J 1961;84:1283-96.
-
(1961)
Can Med Assoc J
, vol.84
, pp. 1283-1296
-
-
Segall, H.N.1
-
7
-
-
0013325922
-
Four cases of 'benign' left bundle branch block in the same family
-
DeForest RE. Four cases of 'benign' left bundle branch block in the same family. Am Heart J 1956;51:398-404.
-
(1956)
Am Heart J
, vol.51
, pp. 398-404
-
-
DeForest, R.E.1
-
9
-
-
2142749053
-
The genetic origin of atrioventricular conduction disturbance in humans
-
discussion 52-9, 76-9
-
Benson DW. The genetic origin of atrioventricular conduction disturbance in humans. Novartis Found Symp 2003;250:242-52; discussion 52-9, 76-9.
-
(2003)
Novartis Found Symp
, vol.250
, pp. 242-252
-
-
Benson, D.W.1
-
10
-
-
0029112853
-
An isolated cardiac conduction disease maps to chromosome 19q
-
de Meeus A, Stephan E, Debrus S, et al . An isolated cardiac conduction disease maps to chromosome 19q. Circ Res 1995;77:735-40.
-
(1995)
Circ Res
, vol.77
, pp. 735-740
-
-
De Meeus, A.1
Stephan, E.2
Debrus, S.3
-
11
-
-
0031022732
-
Hereditary bundle branch defect: Right bundle branch blocks of different causes have different morphologic characteristics
-
Stephan E, de Meeus A, Bouvagnet P. Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristics. Am Heart J 1997;133:249-56.
-
(1997)
Am Heart J
, vol.133
, pp. 249-256
-
-
Stephan, E.1
De Meeus, A.2
Bouvagnet, P.3
-
12
-
-
0003096674
-
Cardiac conduction defects associate with mutations in SCN5A
-
Schott JJ, Alshinawi C, Kyndt F, et al . Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 1999;23:20-1.
-
(1999)
Nat Genet
, vol.23
, pp. 20-21
-
-
Schott, J.J.1
Alshinawi, C.2
Kyndt, F.3
-
13
-
-
45749090058
-
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
-
DOI 10.1172/JCI33891
-
Watanabe H, Koopmann TT, Le Scouarnec S, et al. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin Invest 2008;118:2260-8. (Pubitemid 351872343)
-
(2008)
Journal of Clinical Investigation
, vol.118
, Issue.6
, pp. 2260-2268
-
-
Watanabe, H.1
Koopmann, T.T.2
Le, S.S.3
Yang, T.4
Ingram, C.R.5
Schott, J.-J.6
Demolombe, S.7
Probst, V.8
Anselme, F.9
Escande, D.10
Wiesfeld, A.C.P.11
Pfeufer, A.12
Kaab, S.13
Wichmann, H.-E.14
Hasdemir, C.15
Aizawa, Y.16
Wilde, A.A.M.17
Roden, D.M.18
Bezzina, C.R.19
-
14
-
-
70349215874
-
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type i
-
Kruse M, Schulze-Bahr E, Corfield V, et al. Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I. J Clin Invest 2009;119:2737-44.
-
(2009)
J Clin Invest
, vol.119
, pp. 2737-2744
-
-
Kruse, M.1
Schulze-Bahr, E.2
Corfield, V.3
-
15
-
-
78649264172
-
Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease
-
Liu H, El Zein L, Kruse M, et al. Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease. Circ Cardiovasc Genet 2010;3:374-85.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 374-385
-
-
Liu, H.1
El Zein, L.2
Kruse, M.3
-
16
-
-
33644853792
-
Familial aggregation of calcific aortic valve stenosis in the western part of France
-
Probst V, Le Scouarnec S, Legendre A, et al. Familial aggregation of calcific aortic valve stenosis in the western part of France. Circulation 2006;113:856-60.
-
(2006)
Circulation
, vol.113
, pp. 856-860
-
-
Probst, V.1
Le Scouarnec, S.2
Legendre, A.3
-
17
-
-
64549158495
-
AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram: Part III: Intraventricular conduction disturbances: A scientific statement from the American heart association Electrocardiography and arrhythmias committee, Council on clinical Cardiology; the American College of Cardiology Foundation; and the heart Rhythm Society
-
American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; American College of Cardiology Foundation; Heart Rhythm Society.
-
Surawicz B, Childers R, Deal BJ, et al American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; American College of Cardiology Foundation; Heart Rhythm Society. AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram: part III: intraventricular conduction disturbances: a scientific statement from the American heart association Electrocardiography and arrhythmias committee, Council on clinical Cardiology; the American College of Cardiology Foundation; and the heart Rhythm Society: endorsed by the International Society for Computerized Electrocardiology. Circulation 2009;119:e235-40.
-
(2009)
Circulation
, vol.119
-
-
Surawicz, B.1
Childers, R.2
Deal, B.J.3
-
18
-
-
33947595667
-
Hemiblocks revisited
-
DOI 10.1161/CIRCULATIONAHA.106.637389, PII 0000301720070306000013
-
Elizari MV, Acunzo RS, Ferreiro M. Hemiblocks revisited. Circulation 2007;115:1154-63. (Pubitemid 46673176)
-
(2007)
Circulation
, vol.115
, Issue.9
, pp. 1154-1163
-
-
Elizari, M.V.1
Acunzo, R.S.2
Ferreiro, M.3
-
19
-
-
0037454049
-
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary lenegre disease
-
DOI 10.1016/S0735-1097(02)02864-4
-
Probst V, Kyndt F, Potet F, et al. Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenegre disease. J Am Coll Cardiol 2003;41:643-52. (Pubitemid 36223331)
-
(2003)
Journal of the American College of Cardiology
, vol.41
, Issue.4
, pp. 643-652
-
-
Probst, V.1
Kyndt, F.2
Potet, F.3
Trochu, J.-N.4
Mialet, G.5
Demolombe, S.6
Schott, J.-J.7
Baro, I.8
Escande, D.9
Le, M.H.10
-
20
-
-
0017134190
-
Chronic bifascicular block: Evaluation of familial factors
-
Greenspahn BR, Denes P, Daniel W, et al. Chronic bifascicular block: evaluation of familial factors. Ann Intern Med 1976;84:521-5.
-
(1976)
Ann Intern Med
, vol.84
, pp. 521-525
-
-
Greenspahn, B.R.1
Denes, P.2
Daniel, W.3
-
21
-
-
0022319624
-
Familial fascicular block: Histologic features of Lev's disease
-
DOI 10.1016/0002-8703(85)90377-1
-
Stephan E, Aftimos G, Allam C. Familial fascicular block: histologic features of Lev's disease. Am Heart J 1985; 109:1399-401. (Pubitemid 16119668)
-
(1985)
American Heart Journal
, vol.109
, Issue.6
, pp. 1399-1401
-
-
Stephan, E.1
Aftimos, G.2
Allam, C.3
-
22
-
-
84947899543
-
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
-
Sotoodehnia N, Isaacs A, de Bakker PI, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet 2010;42:1068-76.
-
(2010)
Nat Genet
, vol.42
, pp. 1068-1076
-
-
Sotoodehnia, N.1
Isaacs, A.2
De Bakker, P.I.3
-
23
-
-
79952055695
-
Genetic determinants of cardiac (electric) conduction
-
Priori SG. Genetic determinants of cardiac (electric) conduction. Circ Res 2011;108:402-3.
-
(2011)
Circ Res
, vol.108
, pp. 402-403
-
-
Priori, S.G.1
-
24
-
-
75749102498
-
Genetic variation in SCN10A influences cardiac conduction
-
Chambers JC, Zhao J, Terracciano CM, et al. Genetic variation in SCN10A influences cardiac conduction. Nat Genet 2010;42:149-52.
-
(2010)
Nat Genet
, vol.42
, pp. 149-152
-
-
Chambers, J.C.1
Zhao, J.2
Terracciano, C.M.3
-
25
-
-
75749122164
-
Several common variants modulate heart rate, PR interval and QRS duration
-
Holm H, Gudbjartsson DF, Arnar DO, et al. Several common variants modulate heart rate, PR interval and QRS duration. Nat Genet 2010;42:117-22.
-
(2010)
Nat Genet
, vol.42
, pp. 117-122
-
-
Holm, H.1
Gudbjartsson, D.F.2
Arnar, D.O.3
-
26
-
-
79952257689
-
Genome-wide association studies of the PR interval in African Americans
-
Smith JG, Magnani JW, Palmer C, et al. Genome-wide association studies of the PR interval in African Americans. PLoS Genet 2010;7:e1001304.
-
(2010)
PLoS Genet
, vol.7
-
-
Smith, J.G.1
Magnani, J.W.2
Palmer, C.3
-
27
-
-
75749097235
-
Genome-wide association study of PR interval
-
Pfeufer A, van Noord C, Marciante KD, et al. Genome-wide association study of PR interval. Nat Genet 2010;42:153-9.
-
(2010)
Nat Genet
, vol.42
, pp. 153-159
-
-
Pfeufer, A.1
Van Noord, C.2
Marciante, K.D.3
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