-
1
-
-
77950482741
-
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed modification of the Task Force Criteria
-
Marcus FI, McKenna WJ, Sherrill D et al: Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria. Eur Heart J 2010; 31: 806-814.
-
(2010)
Eur Heart J
, vol.31
, pp. 806-814
-
-
Marcus, F.I.1
McKenna, W.J.2
Sherrill, D.3
-
2
-
-
0035253502
-
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
-
Tiso N, Stephan DA, Nava A et al: Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet 2001; 10: 189-194.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 189-194
-
-
Tiso, N.1
Stephan, D.A.2
Nava, A.3
-
3
-
-
19944426652
-
Regulatory mutations in transforming growth factorbeta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1
-
Beffagna G, Occhi G, Nava A et al: Regulatory mutations in transforming growth factorbeta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. Cardiovasc Res 2005; 65: 366-373.
-
(2005)
Cardiovasc Res
, vol.65
, pp. 366-373
-
-
Beffagna, G.1
Occhi, G.2
Nava, A.3
-
4
-
-
69549138124
-
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
van der Zwaag PA, Jongbloed JD, van den Berg MP et al: A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy. Hum Mutat 2009; 30: 1278-1283.
-
(2009)
Hum Mutat
, vol.30
, pp. 1278-1283
-
-
Van Der Zwaag, P.A.1
Jongbloed, J.D.2
Van Den Berg, M.P.3
-
5
-
-
79959568500
-
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: Pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study
-
Cox MG, van der Zwaag PA, van der Werf C et al: Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study. Circulation 2011; 123: 2690-2700.
-
(2011)
Circulation
, vol.123
, pp. 2690-2700
-
-
Cox, M.G.1
Van Der Zwaag, P.A.2
Van Der Werf, C.3
-
6
-
-
84875901435
-
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy
-
Roberts J, Herkert J, Rutberg J et al: Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy. Clin Genet 2012; 83: 452-456.
-
(2012)
Clin Genet
, vol.83
, pp. 452-456
-
-
Roberts, J.1
Herkert, J.2
Rutberg, J.3
-
7
-
-
84874524757
-
Inherited cardiomyopathies: Molecular genetics and clinical genetic testing in the postgenomic era
-
Teekakirikul P, Kelly MA, Rehm HL, Lakdawala NK, Funke BH: Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era. J Mol Diagn 2013; 15: 158-170.
-
(2013)
J Mol Diagn
, vol.15
, pp. 158-170
-
-
Teekakirikul, P.1
Kelly, M.A.2
Rehm, H.L.3
Lakdawala, N.K.4
Funke, B.H.5
-
8
-
-
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
-
10
-
-
0023848617
-
Right ventricular cardiomyopathy and sudden death in young people
-
Thiene G, Nava A, Corrado D, Rossi L, Pennelli N: Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med 1988; 318: 129-133.
-
(1988)
N Engl J Med
, vol.318
, pp. 129-133
-
-
Thiene, G.1
Nava, A.2
Corrado, D.3
Rossi, L.4
Pennelli, N.5
-
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
-
-
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
-
13
-
-
75249083039
-
Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy
-
Xu T, Yang Z, Vatta M et al: Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy. J Am Coll Cardiol 2010; 55: 587-597.
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 587-597
-
-
Xu, T.1
Yang, Z.2
Vatta, M.3
-
14
-
-
84867736080
-
Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: Evidence supporting the concept of arrhythmogenic cardiomyopathy
-
van der Zwaag PA, van Rijsingen IA, Asimaki A et al: Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy. Eur J Heart Fail 2012; 14: 1199-1207.
-
(2012)
Eur J Heart Fail
, vol.14
, pp. 1199-1207
-
-
Van Der Zwaag, P.A.1
Van Rijsingen, I.A.2
Asimaki, A.3
-
15
-
-
79751479558
-
Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/ dysplasia
-
van der Zwaag PA, Cox MG, van der Werf C et al: Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia. Neth Heart J 2010; 18: 583-591.
-
(2010)
Neth Heart J
, vol.18
, pp. 583-591
-
-
Van Der Zwaag, P.A.1
Cox, M.G.2
Van Der Werf, C.3
-
16
-
-
41649107651
-
Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene
-
Merner ND, Hodgkinson KA, Haywood AF et al: Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. Am J Hum Genet 2008; 82: 809-821.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 809-821
-
-
Merner, N.D.1
Hodgkinson, K.A.2
Haywood, A.F.3
-
17
-
-
77952971659
-
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: Spectrum of mutations and clinical impact in practice
-
Fressart V, Duthoit G, Donal E et al: Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice. Europace 2010; 12: 861-868.
-
(2010)
Europace
, vol.12
, pp. 861-868
-
-
Fressart, V.1
Duthoit, G.2
Donal, E.3
-
18
-
-
72449180918
-
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
-
Bauce B, Nava A, Beffagna G et al: Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/ dysplasia. Heart Rhythm 2010; 7: 22-29.
-
(2010)
Heart Rhythm
, vol.7
, pp. 22-29
-
-
Bauce, B.1
Nava, A.2
Beffagna, G.3
-
19
-
-
79957975773
-
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia- associated mutations from background genetic noise
-
Kapplinger JD, Landstrom AP, Salisbury BA et al: Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise. J Am Coll Cardiol 2011; 57: 2317-2327.
-
(2011)
J Am Coll Cardiol
, vol.57
, pp. 2317-2327
-
-
Kapplinger, J.D.1
Landstrom, A.P.2
Salisbury, B.A.3
-
20
-
-
34247280500
-
Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression
-
Sen-Chowdhry S, Syrris P, Ward D, Asimaki A, Sevdalis E, McKenna WJ: Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression. Circulation 2007; 115: 1710-1720.
-
(2007)
Circulation
, vol.115
, pp. 1710-1720
-
-
Sen-Chowdhry, S.1
Syrris, P.2
Ward, D.3
Asimaki, A.4
Sevdalis, E.5
McKenna, W.J.6
-
21
-
-
33748779315
-
Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: Genotype-phenotype relations, diagnostic features and prognosis
-
Antoniades L, Tsatsopoulou A, Anastasakis A et al: Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis. Eur Heart J 2006; 27: 2208-2216.
-
(2006)
Eur Heart J
, vol.27
, pp. 2208-2216
-
-
Antoniades, L.1
Tsatsopoulou, A.2
Anastasakis, A.3
-
22
-
-
80054971684
-
Safety of endomyocardial biopsy in patients with arrhythmogenic right ventricular cardiomyopathy: A study analyzing 161 diagnostic procedures
-
Paul M, Stypmann J, Gerss J et al: Safety of endomyocardial biopsy in patients with arrhythmogenic right ventricular cardiomyopathy: a study analyzing 161 diagnostic procedures. JACC Cardiovasc Interv 2011; 4: 1142-1148.
-
(2011)
JACC Cardiovasc Interv
, vol.4
, pp. 1142-1148
-
-
Paul, M.1
Stypmann, J.2
Gerss, J.3
-
23
-
-
20544466427
-
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia
-
Corrado D, Basso C, Leoni L et al: Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia. Circulation 2005; 111: 3042-3050.
-
(2005)
Circulation
, vol.111
, pp. 3042-3050
-
-
Corrado, D.1
Basso, C.2
Leoni, L.3
-
24
-
-
84858324575
-
Imaging study of ventricular scar in arrhythmogenic right ventricular cardiomyopathy: Comparison of 3D standard electroanatomical voltage mapping and contrast-enhanced cardiac magnetic resonance
-
Marra MP, Leoni L, Bauce B et al: Imaging study of ventricular scar in arrhythmogenic right ventricular cardiomyopathy: comparison of 3D standard electroanatomical voltage mapping and contrast-enhanced cardiac magnetic resonance. Circ Arrhythm Electrophysiol 2012; 5: 91-100.
-
(2012)
Circ Arrhythm Electrophysiol
, vol.5
, pp. 91-100
-
-
Marra, M.P.1
Leoni, L.2
Bauce, B.3
-
25
-
-
77951112882
-
DNA testing for hypertrophic cardiomyopathy: A cost-effectiveness model
-
Wordsworth S, Leal J, Blair E et al: DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model. Eur Heart J 2010; 31: 926-935.
-
(2010)
Eur Heart J
, vol.31
, pp. 926-935
-
-
Wordsworth, S.1
Leal, J.2
Blair, E.3
-
26
-
-
84874952154
-
The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43
-
Hodgkinson KA, Connors SP, Merner N et al: The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43. Clin Genet 2013; 83: 321-331.
-
(2013)
Clin Genet
, vol.83
, pp. 321-331
-
-
Hodgkinson, K.A.1
Connors, S.P.2
Merner, N.3
|