-
1
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
-
Seidman JG, Seidman C: The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 2001;104:557-567
-
(2001)
Cell
, vol.104
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.2
-
2
-
-
0037070514
-
Hypertrophic cardiomyopathy: A systematic review
-
Maron BJ: Hypertrophic cardiomyopathy: a systematic review. JAMA 2002;287:1308-1320
-
(2002)
JAMA
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
3
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, et al.: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 1992;326:1108-1114
-
(1992)
N Engl J Med
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenzweig, A.2
Hwang, D.S.3
Levi, T.4
McKenna, W.5
-
4
-
-
0032580520
-
Mutation in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Niimura H, Bachinski LL, Sangwatanaroj S, Seidman JG, Seidman CE: Mutation in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 1998;338:1248-1257
-
(1998)
N Engl J Med
, vol.338
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
Seidman, J.G.4
Seidman, C.E.5
-
5
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest SL, Vasile VC, Onimen SR, Will ML, Tajik AJ, et al.: Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol 2004;44:1903-1910
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Onimen, S.R.3
Will, M.L.4
Tajik, A.J.5
-
6
-
-
9444255079
-
Mutations profile in Chinese patients with hypertrophic cardiomyopathy
-
Song L, Zou Y, Wang J, Hui R: Mutations profile in Chinese patients with hypertrophic cardiomyopathy. Clin Chim Acta 2005;351:209-216
-
(2005)
Clin Chim Acta
, vol.351
, pp. 209-216
-
-
Song, L.1
Zou, Y.2
Wang, J.3
Hui, R.4
-
7
-
-
9144224799
-
Prevalence of idiopathic hypertrophic cardiomyopathy in China: A population-based echocardiographic analysis of 8080 adults
-
Zou Y, Song L, Wang Z, Ma A, Liu T, et al.: Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults. Am J Med 2004;116:14-18
-
(2004)
Am J Med
, vol.116
, pp. 14-18
-
-
Zou, Y.1
Song, L.2
Wang, Z.3
Ma, A.4
Liu, T.5
-
8
-
-
0141719865
-
Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: Critical functional sites determine prognosis
-
Woo A, Rakowski H, Liew JC, Zhao MS, Liew CC, et al.: Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis. Heart 2003;89:1179-1185
-
(2003)
Heart
, vol.89
, pp. 1179-1185
-
-
Woo, A.1
Rakowski, H.2
Liew, J.C.3
Zhao, M.S.4
Liew, C.C.5
-
9
-
-
0037461605
-
Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy
-
Maron MS, Olivotto I, Betocchi S, Casey SA, Lesser JR, et al.: Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy. N Engl J Med 2003;348:295-303
-
(2003)
N Engl J Med
, vol.348
, pp. 295-303
-
-
Maron, M.S.1
Olivotto, I.2
Betocchi, S.3
Casey, S.A.4
Lesser, J.R.5
-
10
-
-
0030842476
-
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population
-
Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, et al.: Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population. Circulation 1997;96:214-219
-
(1997)
Circulation
, vol.96
, pp. 214-219
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagege, A.5
-
11
-
-
20544453277
-
Task Force for the Diagnosis and Treatment: Of Chronic Heart Failure of the European Society of Cardiology: Guidelines for the Diagnosis and Treatment of Chronic Heart Failure: Executive Summary (update 2005): The task force for the diagnosis and treatment of chronic heart failure of the European Society of Cardiology
-
Swedberg K, Cleland J, Dargie H, Drexler H, Follath F, et al., Task Force for the Diagnosis and Treatment: of Chronic Heart Failure of the European Society of Cardiology: Guidelines for the Diagnosis and Treatment of Chronic Heart Failure: Executive Summary (update 2005): The task force for the diagnosis and treatment of chronic heart failure of the European Society of Cardiology. Eur Heart J 2005;26:1115-1140
-
(2005)
Eur Heart J
, vol.26
, pp. 1115-1140
-
-
Swedberg, K.1
Cleland, J.2
Dargie, H.3
Drexler, H.4
Follath, F.5
-
12
-
-
0037134832
-
Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: A comprehensive outpatient perspective
-
Ackerman MJ, Van Driest SL, Ommen SR, Will ML, Nishimura RA, et al.: Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective. J Am Coll Cardiol 2002;39:2042-2048
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 2042-2048
-
-
Ackerman, M.J.1
Van Driest, S.L.2
Ommen, S.R.3
Will, M.L.4
Nishimura, R.A.5
-
13
-
-
28744445655
-
Characteristics of the beta myosin heavy chain gene Ala26Val mutation in a Chinese family with hypertrophic cardiomyopathy
-
Liu SX, Hu SJ, Sun J, Wang J, Wang XT, et al.: Characteristics of the beta myosin heavy chain gene Ala26Val mutation in a Chinese family with hypertrophic cardiomyopathy. Eur J Intern Med 2005;16:328-333
-
(2005)
Eur J Intern Med
, vol.16
, pp. 328-333
-
-
Liu, S.X.1
Hu, S.J.2
Sun, J.3
Wang, J.4
Wang, X.T.5
-
14
-
-
0028140230
-
Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical b-myosin heavy chain gene mutations
-
Fananapazir L, Epstein ND: Genotype-phenotype correlations in hypertrophic cardiomyopathy: insights provided by comparisons of kindreds with distinct and identical b-myosin heavy chain gene mutations. Circulation 1994;89:22-32
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananapazir, L.1
Epstein, N.D.2
|