-
1
-
-
9144224799
-
Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults
-
Zou Y., Song L., Wang Z., et al. Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults. Am J Med 116 (2004) 14-18
-
(2004)
Am J Med
, vol.116
, pp. 14-18
-
-
Zou, Y.1
Song, L.2
Wang, Z.3
-
2
-
-
27444445342
-
Distinguishing hypertrophic cardiomyopathy from athlete's heart: a clinical problem of increasing magnitude and significance
-
Maron B.J. Distinguishing hypertrophic cardiomyopathy from athlete's heart: a clinical problem of increasing magnitude and significance. Heart 91 (2005) 1380-1382
-
(2005)
Heart
, vol.91
, pp. 1380-1382
-
-
Maron, B.J.1
-
3
-
-
33847103768
-
Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry
-
Colan S.D., Lipshultz S.E., Lowe A.M., et al. Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry. Circulation 115 (2007) 773-781
-
(2007)
Circulation
, vol.115
, pp. 773-781
-
-
Colan, S.D.1
Lipshultz, S.E.2
Lowe, A.M.3
-
4
-
-
33750121615
-
Incidence, causes, and outcomes of dilated cardiomyopathy in children
-
Towbin J.A., Lowe A.M., Colan S.D., et al. Incidence, causes, and outcomes of dilated cardiomyopathy in children. JAMA 296 (2006) 1867-1876
-
(2006)
JAMA
, vol.296
, pp. 1867-1876
-
-
Towbin, J.A.1
Lowe, A.M.2
Colan, S.D.3
-
5
-
-
0345636017
-
The incidence of pediatric cardiomyopathy in two regions of the United States
-
Lipshultz S.E., Sleeper L.A., Towbin J.A., et al. The incidence of pediatric cardiomyopathy in two regions of the United States. N Engl J Med 348 (2003) 1647-1655
-
(2003)
N Engl J Med
, vol.348
, pp. 1647-1655
-
-
Lipshultz, S.E.1
Sleeper, L.A.2
Towbin, J.A.3
-
6
-
-
30944444021
-
Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes
-
Tardiff J.C. Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes. Heart Fail Rev 10 (2005) 237-248
-
(2005)
Heart Fail Rev
, vol.10
, pp. 237-248
-
-
Tardiff, J.C.1
-
7
-
-
33646757738
-
Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling
-
Ingles J., Doolan A., Chiu C., Seidman J., Seidman C., and Semsarian C. Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling. J Med Genet 42 (2005) e59
-
(2005)
J Med Genet
, vol.42
-
-
Ingles, J.1
Doolan, A.2
Chiu, C.3
Seidman, J.4
Seidman, C.5
Semsarian, C.6
-
8
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest S.L., Vasile V.C., Ommen S.R., et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol 44 (2004) 1903-1910
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
-
9
-
-
0037630018
-
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
Richard P., Charron P., Carrier L., et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 107 (2003) 2227-2232
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
-
10
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
-
Watkins H., McKenna W.J., Thierfelder L., et al. Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med 332 (1995) 1058-1064
-
(1995)
N Engl J Med
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
-
11
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins H., Rosenzweig A., Hwang D.S., et al. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med 326 (1992) 1108-1114
-
(1992)
N Engl J Med
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenzweig, A.2
Hwang, D.S.3
-
12
-
-
0035830394
-
Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis
-
Karibe A., Tobacman L.S., Strand J., et al. Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis. Circulation 103 (2001) 65-71
-
(2001)
Circulation
, vol.103
, pp. 65-71
-
-
Karibe, A.1
Tobacman, L.S.2
Strand, J.3
-
13
-
-
0032499634
-
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene
-
Charron P., Dubourg O., Desnos M., et al. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation 97 (1998) 2230-2236
-
(1998)
Circulation
, vol.97
, pp. 2230-2236
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
-
14
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Niimura H., Bachinski L.L., Sangwatanaroj S., et al. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 338 (1998) 1248-1257
-
(1998)
N Engl J Med
, vol.338
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
-
15
-
-
0042734704
-
Sudden death in young athletes.[see comment]
-
Maron B.J. Sudden death in young athletes.[see comment]. N Engl J Med 349 (2003) 1064-1075
-
(2003)
N Engl J Med
, vol.349
, pp. 1064-1075
-
-
Maron, B.J.1
-
16
-
-
0036117921
-
The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model
-
Semsarian C., Ahmad I., Giewat M., et al. The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model. J Clin Invest 109 (2002) 1013-1020
-
(2002)
J Clin Invest
, vol.109
, pp. 1013-1020
-
-
Semsarian, C.1
Ahmad, I.2
Giewat, M.3
-
17
-
-
0035902491
-
Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy
-
Patel R., Nagueh S.F., Tsybouleva N., et al. Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy. Circulation 104 (2001) 317-324
-
(2001)
Circulation
, vol.104
, pp. 317-324
-
-
Patel, R.1
Nagueh, S.F.2
Tsybouleva, N.3
-
18
-
-
0035852766
-
Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy
-
Lim D.S., Lutucuta S., Bachireddy P., et al. Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy. Circulation 103 (2001) 789-791
-
(2001)
Circulation
, vol.103
, pp. 789-791
-
-
Lim, D.S.1
Lutucuta, S.2
Bachireddy, P.3
-
19
-
-
12144288228
-
Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy
-
Tsybouleva N., Zhang L., Chen S., et al. Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy. Circulation 109 (2004) 1284-1291
-
(2004)
Circulation
, vol.109
, pp. 1284-1291
-
-
Tsybouleva, N.1
Zhang, L.2
Chen, S.3
-
20
-
-
0028872836
-
Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors
-
Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors. Am J Hum Genet 57 (1995) 1233-1241
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1233-1241
-
-
-
21
-
-
25144448782
-
Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey
-
van Langen I.M., Birnie E., Schuurman E., et al. Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey. Clin Genet 68 (2005) 360-368
-
(2005)
Clin Genet
, vol.68
, pp. 360-368
-
-
van Langen, I.M.1
Birnie, E.2
Schuurman, E.3
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