Indexed keywords
ARTICLE;
AUTOSOMAL DOMINANT INHERITANCE;
CHROMOSOME 19Q;
CLINICAL ARTICLE;
FAMILY HISTORY;
FEMALE;
GENE MUTATION;
GENETIC LINKAGE;
GENETIC SUSCEPTIBILITY;
HEART BUNDLE BRANCH BLOCK;
HUMAN;
MALE;
PATHOGENESIS;
PEDIGREE ANALYSIS;
CHROMOSOME 19;
CHROMOSOME MAP;
DISEASE COURSE;
DOMINANT GENE;
ELECTROCARDIOGRAPHY;
GENETICS;
HETEROZYGOTE DETECTION;
PEDIGREE;
POLYMERASE CHAIN REACTION;
PROGNOSIS;
BUNDLE-BRANCH BLOCK;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 19;
DISEASE PROGRESSION;
ELECTROCARDIOGRAPHY;
FEMALE;
GENES, DOMINANT;
HETEROZYGOTE DETECTION;
HUMANS;
MALE;
PEDIGREE;
POLYMERASE CHAIN REACTION;
PROGNOSIS;
1
0000645482
Sur une maladie infantile familiale caractérisée par des modifications permanentes du pouls, des attaques syncopales et épileptiformes et la mort subite
Morquio L. Sur une maladie infantile familiale caractérisée par des modifications permanentes du pouls, des attaques syncopales et épileptiformes et la mort subite. Arch Med Enf 1901 ; 4 : 467-75.
(1901)
Arch Med Enf
, vol.4
, pp. 467-475
Morquio, L.1
2
85046309502
On the so-called Stockes-Adams disease
Osier W. On the so-called Stockes-Adams disease. Lancet 1903 ; 2 : 516-24.
(1903)
Lancet
, vol.2
, pp. 516-524
Osier, W.1
3
26444431689
Bloc auriculoventriculaire chez trois membres d'une même famille
Stéphan E. Bloc auriculoventriculaire chez trois membres d'une même famille. Rev Med Moyen-Orient 1954 ; 11 : 246-9.
(1954)
Rev Med Moyen-Orient
, vol.11
, pp. 246-249
Stéphan, E.1
4
84866231559
Bloc auriculaire familial
Stéphan E. Bloc auriculaire familial. Arch Mal Coeur ; 1961 : 335-41.
(1961)
Arch Mal Coeur
, pp. 335-341
Stéphan, E.1
5
0018570980
Hereditary bundle-branch system defect. A new genetic entity
Stéphan E. Hereditary bundle-branch system defect. A new genetic entity. Am Heart J 1979 ; 97 : 708-18.
(1979)
Am Heart J
, vol.97
, pp. 708-718
Stéphan, E.1
6
0017915484
Hereditary bundle-branch system defect. Survey of a family with four affected generations
Stéphan E. Hereditary bundle-branch system defect. Survey of a family with four affected generations. Am Heart J 1978 ; 95 : 89-95.
(1978)
Am Heart J
, vol.95
, pp. 89-95
Stéphan, E.1
7
0022319624
Familial fascicular bloc. Histologic feature of Lev's disease
Stéphan E, Aftimos G, Allam C. Familial fascicular bloc. Histologic feature of Lev's disease. Am Heart J 1985 ; 109 : 1399-401.
(1985)
Am Heart J
, vol.109
, pp. 1399-1401
Stéphan, E.1
Aftimos, G.2
Allam, C.3
8
0029112853
An isolated cardiac conduction disease maps to chromosome 19q
de Meeus A, Stéphan 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
Stéphan, E.2
Debrus, S.3
10
0014902725
The hemiblocks: Diagnostic criteria and clinical significance
Rosenbaum MB. The hemiblocks: Diagnostic criteria and clinical significance. Mod Concepts Cardiovasc Dis 1970 ; 39 : 141-6.
(1970)
Mod Concepts Cardiovasc Dis
, vol.39
, pp. 141-146
Rosenbaum, M.B.1
11
0009665612
The conduction system
: Could SE (ed). Springfield : Charles C Thomas Publisher
Lev M. The conduction system. In : Could SE (ed). Pathology of the heart and blood vessels. Springfield : Charles C Thomas Publisher, 1968 : 203.
(1968)
Pathology of the Heart and Blood Vessels
, pp. 203
Lev, M.1
12
0031022732
Hereditary bundle branch defect : Right bundle brunch blocks of different causes have different morphologic characteristics
Stéphan E, de Meeus A, Bouvagnet P. Hereditary bundle branch defect : Right bundle brunch blocks of different causes have different morphologic characteristics. Am Heart J 1997 ; 133 : 249-56.
(1997)
Am Heart J
, vol.133
, pp. 249-256
Stéphan, E.1
De Meeus, A.2
Bouvagnet, P.3
13
0017685220
Progressive familial heart block : Two types
Brink AJ, Torrington M. Progressive familial heart block : two types. S Afr Med J 1977 ; 53 : 53-9.
(1977)
S Afr Med J
, vol.53
, pp. 53-59
Brink, A.J.1
Torrington, M.2
14
0028962264
Gene for progressive familial heart block type 1 maps to chromosome 19q13
Brink PA, Ferreira A, Moolman JC, Hettie WW, van der Merwe PL, Corfield VA. Gene for progressive familial heart block type 1 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
Hettie, W.W.4
Van Der Merwe, P.L.5
Corfield, V.A.6