-
1
-
-
61349136209
-
Arrhythmogenic right ventricular cardiomyopathy/ dysplasia: A not so rare "disease of the desmosome" with multiple clinical presentations
-
Herren T, Gerber PA, Duru F. Arrhythmogenic right ventricular cardiomyopathy/ dysplasia: a not so rare "disease of the desmosome" with multiple clinical presentations. Clin Res Cardiol 2009;98:141-158.
-
(2009)
Clin Res Cardiol
, vol.98
, pp. 141-158
-
-
Herren, T.1
Gerber, P.A.2
Duru, F.3
-
2
-
-
11444264507
-
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
-
Gerull B, Heuser A, Wichter T, et al. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet 2004;36:1162-1164.
-
(2004)
Nat Genet
, vol.36
, pp. 1162-1164
-
-
Gerull, B.1
Heuser, A.2
Wichter, T.3
-
3
-
-
4944253790
-
Natural history and risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
Hulot J-S, Jouven X, Empana J-P, et al. Natural history and risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation 2004; 110:1879-1884.
-
(2004)
Circulation
, vol.110
, pp. 1879-1884
-
-
Hulot, J.-S.1
Jouven, X.2
Empana, J.-P.3
-
4
-
-
0028347223
-
Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology
-
McKenna WJ, Thiene G, Nava A, et al. Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. Br Heart J 1994;71:215-218.
-
(1994)
Br Heart J
, vol.71
, pp. 215-218
-
-
McKenna, W.J.1
Thiene, G.2
Nava, A.3
-
5
-
-
0033951027
-
Follow-up of patients with arrhythmogenic right ventricular cardiomyopathy dysplasia
-
Munclinger MJ, Patel JJ, Mitha AS. Follow-up of patients with arrhythmogenic right ventricular cardiomyopathy dysplasia. S Afr Med J 2000;90:61-68.
-
(2000)
S Afr Med J
, vol.90
, pp. 61-68
-
-
Munclinger, M.J.1
Patel, J.J.2
Mitha, A.S.3
-
6
-
-
33646002657
-
Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): Support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes
-
Matolweni L, Bardien S, Rebello G, et al. Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes. BMC Med Genet 2006;7:29.
-
(2006)
BMC Med Genet
, vol.7
, pp. 29
-
-
Matolweni, L.1
Bardien, S.2
Rebello, G.3
-
7
-
-
33644876781
-
Epidemiology and etiology of cardiomyopathy in Africa
-
Sliwa K, Damasceno A, Mayosi BM. Epidemiology and etiology of cardiomyopathy in Africa. Circulation 2005;112:3577-3583.
-
(2005)
Circulation
, vol.112
, pp. 3577-3583
-
-
Sliwa, K.1
Damasceno, A.2
Mayosi, B.M.3
-
8
-
-
17444438135
-
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: Need for an international registry
-
Corrado D, Fontaine G, Marcus FI, et al. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: need for an international registry. Circulation 2000; 101:101e-106e.
-
(2000)
Circulation
, vol.101
-
-
Corrado, D.1
Fontaine, G.2
Marcus, F.I.3
-
9
-
-
33645772930
-
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
van Tintelen JP, Entius MM, Bhuiyan ZA, 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
-
10
-
-
41949088366
-
Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy
-
Lahtinen AM, Lehtonen A, Kaartinen M, et al. Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy. Int J Cardiol 2008;126:92-100.
-
(2008)
Int J Cardiol
, vol.126
, pp. 92-100
-
-
Lahtinen, A.M.1
Lehtonen, A.2
Kaartinen, M.3
-
11
-
-
33644851952
-
Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy
-
Syrris P, Ward D, Asimaki A, et al. Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy. Circulation 2006;113:356-364.
-
(2006)
Circulation
, vol.113
, pp. 356-364
-
-
Syrris, P.1
Ward, D.2
Asimaki, A.3
-
12
-
-
33645787474
-
Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2
-
Dalal D, Molin LH, Piccini J, et al. Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2. Circulation 2006;113:1641-1649.
-
(2006)
Circulation
, vol.113
, pp. 1641-1649
-
-
Dalal, D.1
Molin, L.H.2
Piccini, J.3
-
13
-
-
33646698000
-
Initial report of the Arrhythmogenic Right Ventricular Cardiomyopathy Registry of South Africa: 2004
-
Latib MA, Michaels K, Mayosi BM. Initial report of the Arrhythmogenic Right Ventricular Cardiomyopathy Registry of South Africa: 2004. Cardiovasc J S Afr 2004;15:237-238.
-
(2004)
Cardiovasc J S Afr
, vol.15
, pp. 237-238
-
-
Latib, M.A.1
Michaels, K.2
Mayosi, B.M.3
-
14
-
-
0037120964
-
Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria
-
Hamid MS, Norman M, Quraishi A, et al. Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria. J Am Coll Cardiol 2002;40:1445-1450.
-
(2002)
J Am Coll Cardiol
, vol.40
, pp. 1445-1450
-
-
Hamid, M.S.1
Norman, M.2
Quraishi, A.3
-
15
-
-
0033361790
-
The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: A unique profile of both independent and founder events
-
Moolman-Smook JC, De Lange WJ, Bruwer EC, et al. The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events. Am J Hum Genet 1999;65:1308-1320.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1308-1320
-
-
Moolman-Smook, J.C.1
De Lange, W.J.2
Bruwer, E.C.3
-
16
-
-
33644878722
-
Arrhythmogenic right ventricular dysplasia: A United States experience
-
Dalal D, Nasir K, Bomma C, et al. Arrhythmogenic right ventricular dysplasia: a United States experience. Circulation 2005;112:3823-3832.
-
(2005)
Circulation
, vol.112
, pp. 3823-3832
-
-
Dalal, D.1
Nasir, K.2
Bomma, C.3
-
17
-
-
0020077022
-
Right ventricular dysplasia: A report of 24 adult cases
-
Marcus FI, Fontaine GH, Guiraudon G, et al. Right ventricular dysplasia: a report of 24 adult cases. Circulation 1982;65:384-398.
-
(1982)
Circulation
, vol.65
, pp. 384-398
-
-
Marcus, F.I.1
Fontaine, G.H.2
Guiraudon, G.3
-
18
-
-
0030712343
-
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: A multicenter study
-
Corrado D, Basso C, Thiene G, et al. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J Am Coll Cardiol 1997;30:1512-1520.
-
(1997)
J Am Coll Cardiol
, vol.30
, pp. 1512-1520
-
-
Corrado, D.1
Basso, C.2
Thiene, G.3
-
19
-
-
0033662201
-
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
-
Nava A, Bauce B, Basso C, et al. Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. J Am Coll Cardiol 2000;36:2226-2233.
-
(2000)
J Am Coll Cardiol
, vol.36
, pp. 2226-2233
-
-
Nava, A.1
Bauce, B.2
Basso, C.3
-
20
-
-
27444442331
-
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population
-
Brink PA, Crotti L, Corfield V, et al. Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population. Circulation 2005;112:2602-2610.
-
(2005)
Circulation
, vol.112
, pp. 2602-2610
-
-
Brink, P.A.1
Crotti, L.2
Corfield, V.3
-
21
-
-
0029832024
-
Founder effect and prevalence of myotonic dystrophy in South Africans: Molecular studies
-
Goldman A, Krause A, Ramsay M, et al. Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies. Am J Hum Genet 1996;59:445-452.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 445-452
-
-
Goldman, A.1
Krause, A.2
Ramsay, M.3
-
22
-
-
0031971162
-
Linkage disequilibrium analysis in a recently founded population: Evaluation of the variegate porphyria founder in South African Afrikaners
-
Groenewald JZ, Liebenberg L, Groenewald IM, et al. Linkage disequilibrium analysis in a recently founded population: evaluation of the variegate porphyria founder in South African Afrikaners. Am J Hum Genet 1998;62:1254-1258.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1254-1258
-
-
Groenewald, J.Z.1
Liebenberg, L.2
Groenewald, I.M.3
-
23
-
-
0027429315
-
Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations
-
Kotze MJ, De Villiers WJ, Steyn K, et al. Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations. Arterioscler Thromb Vasc Biol 1993;13:1460-1468.
-
(1993)
Arterioscler Thromb Vasc Biol
, vol.13
, pp. 1460-1468
-
-
Kotze, M.J.1
De Villiers, W.J.2
Steyn, K.3
-
24
-
-
0036820764
-
Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa
-
Le Saux O, Beck K, Sachsinger C, et al. Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa. Hum Genet 2002;111:331-338.
-
(2002)
Hum Genet
, vol.111
, pp. 331-338
-
-
Le Saux, O.1
Beck, K.2
Sachsinger, C.3
-
25
-
-
14344284734
-
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa
-
Tipping AJ, Pearson T, Morgan NV, et al. Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa. Proc Natl Acad Sci U S A 2001;98:5734-5739.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 5734-5739
-
-
Tipping, A.J.1
Pearson, T.2
Morgan, N.V.3
-
26
-
-
0031671266
-
The 1995 survey of cardiac pacing in South Africa
-
Mayosi BM, Millar RS. The 1995 survey of cardiac pacing in South Africa. S Afr Med J 1988;88(Cardiovasc Suppl 4):C207-C11.
-
(1988)
S Afr Med J
, vol.88
, Issue.SUPPL. 4
-
-
Mayosi, B.M.1
Millar, R.S.2
-
27
-
-
0025760935
-
Medicine and healthcare in south Africa
-
Benatar SR. Medicine and healthcare in south Africa. N Engl J Med 1991;325: 30-36.
-
(1991)
N Engl J Med
, vol.325
, pp. 30-36
-
-
Benatar, S.R.1
-
28
-
-
0041629662
-
High prevalence of right ventricular involvement in endurance athletes with ventricular arrhythmias: Role of an electrophysiologic study in risk stratification
-
Heidbuchel H, Hoogsteen J, Fagard R, et al. High prevalence of right ventricular involvement in endurance athletes with ventricular arrhythmias: role of an electrophysiologic study in risk stratification. Eur Heart J 2003; 24:1473-1480.
-
(2003)
Eur Heart J
, vol.24
, pp. 1473-1480
-
-
Heidbuchel, H.1
Hoogsteen, J.2
Fagard, R.3
-
29
-
-
33750539318
-
Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice
-
Kirchhof P, Fabritz L, Zwiener M, et al. Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice. Circulation 2006;114:1799-1806.
-
(2006)
Circulation
, vol.114
, pp. 1799-1806
-
-
Kirchhof, P.1
Fabritz, L.2
Zwiener, M.3
-
30
-
-
42649092901
-
Mechanisms of disease: Molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
Awad MM, Calkins H, Judge DP. Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Nat Clin Pract Cardiovasc Med 2008;5:258-267.
-
(2008)
Nat Clin Pract Cardiovasc Med
, vol.5
, pp. 258-267
-
-
Awad, M.M.1
Calkins, H.2
Judge, D.P.3
-
31
-
-
20044380514
-
Cardiovascular pre-participation screening of young competitive athletes for prevention of sudden death: Proposal for a common European protocol: Consensus Statement of the Study Group of Sport Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology
-
Corrado D, Pelliccia A, Bjornstad HH, et al. Cardiovascular pre-participation screening of young competitive athletes for prevention of sudden death: proposal for a common European protocol: Consensus Statement of the Study Group of Sport Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology. Eur Heart J 2005;26:516-524.
-
(2005)
Eur Heart J
, vol.26
, pp. 516-524
-
-
Corrado, D.1
Pelliccia, A.2
Bjornstad, H.H.3
-
32
-
-
69949096470
-
The burden of noncommunicable diseases in South Africa
-
Mayosi BM, Flisher AJ, Lalloo UG, et al. The burden of noncommunicable diseases in South Africa. The Lancet 2009;374:934-947.
-
(2009)
The Lancet
, vol.374
, pp. 934-947
-
-
Mayosi, B.M.1
Flisher, A.J.2
Lalloo, U.G.3
-
34
-
-
34147208940
-
Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2
-
Awad M, Dalal D, Tichnell C, et al. Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2. Hum Mutat 2006;27: 1157.
-
(2006)
Hum Mutat
, vol.27
, pp. 1157
-
-
Awad, M.1
Dalal, D.2
Tichnell, C.3
|