-
1
-
-
33645655544
-
Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: Septal morphological features predict the presence of myofilament mutations
-
Binder J, Ommen SR, Gersh BJ, Van Driest SL, Tajik AJ, Nishimura RA, Ackerman MJ. Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: Septal morphological features predict the presence of myofilament mutations. Mayo Clin Proc 2006 81 : 459 467.
-
(2006)
Mayo Clin Proc
, vol.81
, pp. 459-467
-
-
Binder, J.1
Ommen, S.R.2
Gersh, B.J.3
Van Driest, S.L.4
Tajik, A.J.5
Nishimura, R.A.6
Ackerman, M.J.7
-
2
-
-
0142104868
-
The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
-
Alders M, Jongbloed R, Deelen W, Van den Wijngaard A, Doevendans P, Ten Cate F, Regitz-Zagrosek V, et al. The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands. Eur Heart J 2003 24 : 1848 1853.
-
(2003)
Eur Heart J
, vol.24
, pp. 1848-1853
-
-
Alders, M.1
Jongbloed, R.2
Deelen, W.3
Van Den Wijngaard, A.4
Doevendans, P.5
Ten Cate, F.6
Regitz-Zagrosek, V.7
-
3
-
-
33750852724
-
Can electrocardiographic changes help to identify the causative mutation in hereditary hypertrophic cardiomyopathy?
-
Arens YH, Hermans JF, Kuusisto J, Jaaskelainen P, Chai W, Wilde AA, Pinto YM. Can electrocardiographic changes help to identify the causative mutation in hereditary hypertrophic cardiomyopathy? Suppl Circul 2005 112 : II 604.
-
(2005)
Suppl Circul
, vol.112
-
-
Arens, Y.H.1
Hermans, J.F.2
Kuusisto, J.3
Jaaskelainen, P.4
Chai, W.5
Wilde, A.A.6
Pinto, Y.M.7
-
5
-
-
0037058868
-
Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy
-
Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, et al. Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy. Circulation 2002 106 : 3085 3090.
-
(2002)
Circulation
, vol.106
, pp. 3085-3090
-
-
Van Driest, S.L.1
Ackerman, M.J.2
Ommen, S.R.3
Shakur, R.4
Will, M.L.5
Nishimura, R.A.6
Tajik, A.J.7
-
6
-
-
21344441228
-
Genetics and cardiomyopathy: Where are we now?
-
Murphy RT, Starling RC. Genetics and cardiomyopathy: Where are we now? Cleve Clin J Med 2005 72 : 465 483.
-
(2005)
Cleve Clin J Med
, vol.72
, pp. 465-483
-
-
Murphy, R.T.1
Starling, R.C.2
-
7
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharm P, McDonough B, Smoot L, et al. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med 2000 7 343 : 1688 1696.
-
(2000)
N Engl J Med
, vol.7
, Issue.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
Depalma, S.R.3
Solomon, S.4
Sharm, P.5
McDonough, B.6
Smoot, L.7
-
8
-
-
19944431159
-
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: Do lamin A/C mutations portend a high risk of sudden death?
-
Van Berlo JH, de Voogt WG, Van Der Kooi AJ, Van Tintelen JP, Bonne G, Ben Yaou R, Duboc D, et al. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: Do lamin A/C mutations portend a high risk of sudden death? J Mol Med 2005 83 : 79 83.
-
(2005)
J Mol Med
, vol.83
, pp. 79-83
-
-
Van Berlo, J.H.1
De Voogt, W.G.2
Van Der Kooi, A.J.3
Van Tintelen, J.P.4
Bonne, G.5
Ben Yaou, R.6
Duboc, D.7
-
9
-
-
5644229494
-
SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia
-
McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, Mestroni L et al. SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. Circulation 2004 110 : 2163 2167.
-
(2004)
Circulation
, vol.110
, pp. 2163-2167
-
-
McNair, W.P.1
Ku, L.2
Taylor, M.R.3
Fain, P.R.4
Dao, D.5
Wolfel, E.6
Mestroni, L.7
-
10
-
-
30444446953
-
Primary prevention of sudden death in patients with lamin A/C gene mutations
-
Meune C, Van Berlo JH, Anselme F, Bonne G, Pinto YP, Duboc D. Primary prevention of sudden death in patients with lamin A/C gene mutations. N Engl J Med 2006 12 354 : 209 210.
-
(2006)
N Engl J Med
, vol.12
, Issue.354
, pp. 209-210
-
-
Meune, C.1
Van Berlo, J.H.2
Anselme, F.3
Bonne, G.4
Pinto, Y.P.5
Duboc, D.6
-
11
-
-
34147206221
-
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: Emerging horizon?
-
van Tintelen JP, Hofstra RM, Wiesfeld AC, Van den Berg MP, Hauer RNW, Jongbloed JDH. Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: Emerging horizon? Curr Opin Cardiol 2007 22 : 185 192.
-
(2007)
Curr Opin Cardiol
, vol.22
, pp. 185-192
-
-
Van Tintelen, J.P.1
Hofstra, R.M.2
Wiesfeld, A.C.3
Van Den Berg, M.P.4
Hauer, R.N.W.5
Jongbloed, J.D.H.6
-
12
-
-
33748934196
-
Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
Dalal D, James C, Devanagondi R, Tichnell C, Tucker A, Prakasa K, Spevak PJ, et al. Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Am Coll Cardiol 2006 48 : 1416 1424.
-
(2006)
J Am Coll Cardiol
, vol.48
, pp. 1416-1424
-
-
Dalal, D.1
James, C.2
Devanagondi, R.3
Tichnell, C.4
Tucker, A.5
Prakasa, K.6
Spevak, P.J.7
-
13
-
-
33645772930
-
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld ACP, Wilde AAM, Van der Smagt J, et al. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation 2006 113 : 1650 1658.
-
(2006)
Circulation
, vol.113
, pp. 1650-1658
-
-
Van Tintelen, J.P.1
Entius, M.M.2
Bhuiyan, Z.A.3
Jongbloed, R.4
Wiesfeld, A.C.P.5
Wilde, A.A.M.6
Van Der Smagt, J.7
-
14
-
-
19944433030
-
The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
-
Hodgkinson KA, Parfrey PS, Bassett AS, Kupprion C, Drenkhahn J, Norman MW, Thierfelder L, et al. The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5). J Am Coll Cardiol 2005 45 : 4000 4008.
-
(2005)
J Am Coll Cardiol
, vol.45
, pp. 4000-4008
-
-
Hodgkinson, K.A.1
Parfrey, P.S.2
Bassett, A.S.3
Kupprion, C.4
Drenkhahn, J.5
Norman, M.W.6
Thierfelder, L.7
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