-
1
-
-
0020066017
-
Sudden death in hypertrophic cardiomyopathy: A profile in 78 patients
-
Maron BJ, Roberts WC, Epstein SE. Sudden death in hypertrophic cardiomyopathy: a profile in 78 patients. Circulation 1982;67:1388-1394.
-
(1982)
Circulation
, vol.67
, pp. 1388-1394
-
-
Maron, B.J.1
Roberts, W.C.2
Epstein, S.E.3
-
2
-
-
0024522202
-
Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population
-
Spirito P, Chiarella E, Carratio L, Berisso MZ, Bellotti P, Vecchio C. Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population. N Engl J Med 1989;320:749-755.
-
(1989)
N Engl J Med
, vol.320
, pp. 749-755
-
-
Spirito, P.1
Chiarella, E.2
Carratio, L.3
Berisso, M.Z.4
Bellotti, P.5
Vecchio, C.6
-
3
-
-
0023269245
-
Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilation in patients with hypertrophic cardiomyopathy
-
Spirito P, Maron BJ, Bonow RO, Epstein SE. Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilation in patients with hypertrophic cardiomyopathy. Am J Cardiol 1987;60:123-129.
-
(1987)
Am J Cardiol
, vol.60
, pp. 123-129
-
-
Spirito, P.1
Maron, B.J.2
Bonow, R.O.3
Epstein, S.E.4
-
4
-
-
0027247910
-
Coexistence of sudden cardiac death and end-stage heart failure in familial hypertrophic cardiomyopathy
-
Hecht GM, Klues HG, Roberts WC, Maron BJ. Coexistence of sudden cardiac death and end-stage heart failure in familial hypertrophic cardiomyopathy. J Am Coll Cardiol 1993;22:489-497.
-
(1993)
J Am Coll Cardiol
, vol.22
, pp. 489-497
-
-
Hecht, G.M.1
Klues, H.G.2
Roberts, W.C.3
Maron, B.J.4
-
5
-
-
0029922379
-
Apoptosis as a possible cause of gradual development of complete heart block and fatal arrhythmias associated with absence of the AV node, sinus node, and internodal pathways
-
James TN, Martin E, Willis PW III, Lohr TO. Apoptosis as a possible cause of gradual development of complete heart block and fatal arrhythmias associated with absence of the AV node, sinus node, and internodal pathways. Circulation 1996;93:1424-1438.
-
(1996)
Circulation
, vol.93
, pp. 1424-1438
-
-
James, T.N.1
Martin, E.2
Willis P.W. III3
Lohr, T.O.4
-
6
-
-
0021705107
-
Progression from hypertrophic obstructive cardiomyopathy to typical dilated cardiomyopathy-like features in the end stage
-
Fujiwara H, Onodera T, Tanaka M, Shirane H, Kato H, Yoshikawa J, Osakada G, Sasayama S, Kawai C. Progression from hypertrophic obstructive cardiomyopathy to typical dilated cardiomyopathy-like features in the end stage. Jpn Circ J 1984;48:1210-1214.
-
(1984)
Jpn Circ J
, vol.48
, pp. 1210-1214
-
-
Fujiwara, H.1
Onodera, T.2
Tanaka, M.3
Shirane, H.4
Kato, H.5
Yoshikawa, J.6
Osakada, G.7
Sasayama, S.8
Kawai, C.9
-
7
-
-
0021222527
-
Seventeen year follow-up of a patient with hypertrophic cardiomyopathy which progressed to dilated cardiomyopathy
-
Funakoshi M, Imamura M, Sasaki J, Fujino M, Kawano T, Sasaki Y, Nakashima Y, Motooka T, Fukuda K, Imagawa M, Hiroki T, Arakawa K. Seventeen year follow-up of a patient with hypertrophic cardiomyopathy which progressed to dilated cardiomyopathy. Jpn Heart J 1984;25:805-809.
-
(1984)
Jpn Heart J
, vol.25
, pp. 805-809
-
-
Funakoshi, M.1
Imamura, M.2
Sasaki, J.3
Fujino, M.4
Kawano, T.5
Sasaki, Y.6
Nakashima, Y.7
Motooka, T.8
Fukuda, K.9
Imagawa, M.10
Hiroki, T.11
Arakawa, K.12
-
8
-
-
0018761299
-
Hypertrophic cardiomyopathy and transmural myocardial infarction without significant atherosclerosis of the extramural coronary arteries
-
Maron BJ, Epstein SE, Roberts WC. Hypertrophic cardiomyopathy and transmural myocardial infarction without significant atherosclerosis of the extramural coronary arteries. Am J Cardiol 1979;43:1086-1102.
-
(1979)
Am J Cardiol
, vol.43
, pp. 1086-1102
-
-
Maron, B.J.1
Epstein, S.E.2
Roberts, W.C.3
-
9
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familiar hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder L, Watkins H, WacRae C, Lamas R, McKenna WJ, Vosberg H-P, Seidman JG, Seidman CE. α-Tropomyosin and cardiac troponin T mutations cause familiar hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 1994;77:701-702.
-
(1994)
Cell
, vol.77
, pp. 701-702
-
-
Thierfelder, L.1
Watkins, H.2
WacRae, C.3
Lamas, R.4
McKenna, W.J.5
Vosberg, H.-P.6
Seidman, J.G.7
Seidman, C.E.8
-
10
-
-
0025104401
-
Familiar hypertrophic cardiomyopathy is a genetically heterogeneous disease
-
Solomon SD, Jarcho JA, MacKenna WJ, Geisterfer-Lowrance A, Germain R, Malerni R, Seidman JG, Seidman CE. Familiar hypertrophic cardiomyopathy is a genetically heterogeneous disease. J Clin Invest 1990;86:993-999.
-
(1990)
J Clin Invest
, vol.86
, pp. 993-999
-
-
Solomon, S.D.1
Jarcho, J.A.2
MacKenna, W.J.3
Geisterfer-Lowrance, A.4
Germain, R.5
Malerni, R.6
Seidman, J.G.7
Seidman, C.E.8
|