-
1
-
-
33646693410
-
Contemporary definitions and classification of the cardiomyopathies: An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; And Council on Epidemiology and Prevention
-
B.J. Maron, J.A. Towbin, and G. Thiene et al. Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention Circulation 113 2006 1807 1816
-
(2006)
Circulation
, vol.113
, pp. 1807-1816
-
-
Maron, B.J.1
Towbin, J.A.2
Thiene, G.3
-
2
-
-
38349086961
-
Classification of the cardiomyopathies: A position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
-
P. Elliott, B. Andersson, and E. Arbustini et al. Classification of the cardiomyopathies: a position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases Eur Heart J 29 2008 270 276
-
(2008)
Eur Heart J
, vol.29
, pp. 270-276
-
-
Elliott, P.1
Andersson, B.2
Arbustini, E.3
-
3
-
-
84904541589
-
-
United Healthcare. Accessed June 5, 2014
-
United Healthcare. Available at: http://www.acc.org/clinical/statements. html. Accessed June 5, 2014.
-
-
-
-
4
-
-
0031885093
-
Familial dilated cardiomyopathy: Cardiac abnormalities are common in asymptomatic relatives and may represent early disease
-
M.K. Baig, J.H. Goldman, and A.L. Caforio et al. Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease J Am Coll Cardiol 31 1998 195 201
-
(1998)
J Am Coll Cardiol
, vol.31
, pp. 195-201
-
-
Baig, M.K.1
Goldman, J.H.2
Caforio, A.L.3
-
5
-
-
0034944490
-
Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics
-
A. Gavazzi, A. Repetto, and L. Scelsi et al. Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics Eur Heart J 22 2001 73 81
-
(2001)
Eur Heart J
, vol.22
, pp. 73-81
-
-
Gavazzi, A.1
Repetto, A.2
Scelsi, L.3
-
6
-
-
20044396901
-
Natural history and familial characteristics of isolated left ventricular non-compaction
-
R.T. Murphy, R. Thaman, and J.G. Blanes et al. Natural history and familial characteristics of isolated left ventricular non-compaction Eur Heart J 26 2005 187 192
-
(2005)
Eur Heart J
, vol.26
, pp. 187-192
-
-
Murphy, R.T.1
Thaman, R.2
Blanes, J.G.3
-
7
-
-
22244436280
-
Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease
-
N.G. Mahon, R.T. Murphy, and C.A. MacRae et al. Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease Ann Intern Med 143 2005 108 115
-
(2005)
Ann Intern Med
, vol.143
, pp. 108-115
-
-
Mahon, N.G.1
Murphy, R.T.2
Macrae, C.A.3
-
8
-
-
0031049263
-
Experience from clinical genetics in hypertrophic cardiomyopathy: Proposal for new diagnostic criteria in adult members of affected families
-
W.J. McKenna, P. Spirito, and M. Desnos et al. Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families Heart 77 1997 130 132
-
(1997)
Heart
, vol.77
, pp. 130-132
-
-
McKenna, W.J.1
Spirito, P.2
Desnos, M.3
-
9
-
-
0033662201
-
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
-
A. Nava, B. Bauce, and C. Basso et al. Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy J Am Coll Cardiol 36 2000 2226 2233
-
(2000)
J Am Coll Cardiol
, vol.36
, pp. 2226-2233
-
-
Nava, A.1
Bauce, B.2
Basso, C.3
-
10
-
-
0037120964
-
Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria
-
M.S. Hamid, M. Norman, and A. Quraishi et al. Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria J Am Coll Cardiol 40 2002 1445 1450
-
(2002)
J Am Coll Cardiol
, vol.40
, pp. 1445-1450
-
-
Hamid, M.S.1
Norman, M.2
Quraishi, A.3
-
11
-
-
84883746417
-
Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
-
European Society of Cardiology Working Group on Myocardial and Pericardial Diseases 2648a-2648d
-
A.L. Caforio, S. Pankuweit, E. Arbustini European Society of Cardiology Working Group on Myocardial and Pericardial Diseases Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases Eur Heart J 34 2013 2636 2648 2648a-2648d
-
(2013)
Eur Heart J
, vol.34
, pp. 2636-2648
-
-
Caforio, A.L.1
Pankuweit, S.2
Arbustini, E.3
-
12
-
-
84856703950
-
Genetics of inherited cardiomyopathy
-
D. Jacoby, and W.J. McKenna Genetics of inherited cardiomyopathy Eur Heart J 33 2012 296 304
-
(2012)
Eur Heart J
, vol.33
, pp. 296-304
-
-
Jacoby, D.1
McKenna, W.J.2
-
14
-
-
84865127014
-
Genetics of hypertrophic cardiomyopathy after 20 years: Clinical perspectives
-
B.J. Maron, M.S. Maron, and C. Semsarian Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives J Am Coll Cardiol 60 2012 705 715
-
(2012)
J Am Coll Cardiol
, vol.60
, pp. 705-715
-
-
Maron, B.J.1
Maron, M.S.2
Semsarian, C.3
-
15
-
-
84888066429
-
A systematic review and meta-analysis of genotype-phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations
-
L.R. Lopes, M.S. Rahman, and P.M. Elliott A systematic review and meta-analysis of genotype-phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations Heart 99 2013 1800 1811
-
(2013)
Heart
, vol.99
, pp. 1800-1811
-
-
Lopes, L.R.1
Rahman, M.S.2
Elliott, P.M.3
-
16
-
-
78649373427
-
Genetic counselling and testing in cardiomyopathies: A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
-
P. Charron, M. Arad, and E. Arbustini et al. Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases Eur Heart J 3 2010 2715 2726
-
(2010)
Eur Heart J
, vol.3
, pp. 2715-2726
-
-
Charron, P.1
Arad, M.2
Arbustini, E.3
-
17
-
-
84877956038
-
Diagnostic work-up in cardiomyopathies: Bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases
-
C. Rapezzi, E. Arbustini, and A.P.L. Caforio et al. Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases Eur Heart J 34 2013 1448 1458
-
(2013)
Eur Heart J
, vol.34
, pp. 1448-1458
-
-
Rapezzi, C.1
Arbustini, E.2
Caforio, A.P.L.3
-
18
-
-
84872778197
-
The prognostic value of late gadolinium enhancement CMR in nonischemic cardiomyopathies
-
T.D. Karamitsos, and S. Neubauer The prognostic value of late gadolinium enhancement CMR in nonischemic cardiomyopathies Curr Cardiol Rep 15 2013 326
-
(2013)
Curr Cardiol Rep
, vol.15
, pp. 326
-
-
Karamitsos, T.D.1
Neubauer, S.2
-
19
-
-
84865589333
-
Cardiomyopathies: Focus on cardiovascular magnetic resonance
-
G. Quarta, D.M. Sado, and J.C. Moon Cardiomyopathies: focus on cardiovascular magnetic resonance Br J Radiol 84 2011 S296 S305
-
(2011)
Br J Radiol
, vol.84
-
-
Quarta, G.1
Sado, D.M.2
Moon, J.C.3
-
20
-
-
33747180877
-
Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects
-
E. Arbustini, M. Pasotti, and A. Pilotto et al. Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects Eur J Heart Fail 8 2006 477 483
-
(2006)
Eur J Heart Fail
, vol.8
, pp. 477-483
-
-
Arbustini, E.1
Pasotti, M.2
Pilotto, A.3
-
21
-
-
0036899547
-
The need for European Registries in inherited cardiomyopathies
-
Myocardial and Pericardial Working Group of the European Society of Cardiology
-
E. Arbustini, F. Cecchi, O. Dubourg Myocardial and Pericardial Working Group of the European Society of Cardiology The need for European Registries in inherited cardiomyopathies Eur Heart J 23 2002 1972 1974
-
(2002)
Eur Heart J
, vol.23
, pp. 1972-1974
-
-
Arbustini, E.1
Cecchi, F.2
Dubourg, O.3
-
22
-
-
84876276624
-
Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy
-
National Heart, Lung, and Blood Institute GO Exome Sequencing Project and the Exome Sequencing Project Family Studies Project Team
-
N. Norton, D. Li, E. Rampersaud National Heart, Lung, and Blood Institute GO Exome Sequencing Project and the Exome Sequencing Project Family Studies Project Team Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy Circ Cardiovasc Genet 6 2013 144 153
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 144-153
-
-
Norton, N.1
Li, D.2
Rampersaud, E.3
-
23
-
-
79953842000
-
Update 2011: Clinical and genetic issues in familial dilated cardiomyopathy
-
R.E. Hershberger, and J.D. Siegfried Update 2011: clinical and genetic issues in familial dilated cardiomyopathy J Am Coll Cardiol 57 2011 1641 1649
-
(2011)
J Am Coll Cardiol
, vol.57
, pp. 1641-1649
-
-
Hershberger, R.E.1
Siegfried, J.D.2
-
24
-
-
0024426784
-
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1
-
J.A. Jarcho, W. McKenna, and J.A. Pare et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1 N Engl J Med 321 1989 1372 1378
-
(1989)
N Engl J Med
, vol.321
, pp. 1372-1378
-
-
Jarcho, J.A.1
McKenna, W.2
Pare, J.A.3
-
25
-
-
84899538064
-
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy
-
B. Meder, F. Rühle, and T. Weis et al. A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy Eur Heart J 35 2014 1069 1077
-
(2014)
Eur Heart J
, vol.35
, pp. 1069-1077
-
-
Meder, B.1
Rühle, F.2
Weis, T.3
-
26
-
-
80052186988
-
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
-
E. Villard, C. Perret, and F. Gary et al. A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy Eur Heart J 32 2011 1065 1076
-
(2011)
Eur Heart J
, vol.32
, pp. 1065-1076
-
-
Villard, E.1
Perret, C.2
Gary, F.3
-
27
-
-
84883163817
-
Dilated cardiomyopathy: The complexity of a diverse genetic architecture
-
R.E. Hershberger, D.J. Hedges, and A. Morales Dilated cardiomyopathy: the complexity of a diverse genetic architecture Nature Rev Cardiol 10 2013 531
-
(2013)
Nature Rev Cardiol
, vol.10
, pp. 531
-
-
Hershberger, R.E.1
Hedges, D.J.2
Morales, A.3
-
28
-
-
84878195274
-
Arrhythmogenic right ventricular cardiomyopathy (ARVC/D): A systematic literature review
-
J. Romero, E. Mejia-Lopez, and C. Manrique et al. Arrhythmogenic right ventricular cardiomyopathy (ARVC/D): a systematic literature review Clin Med Insights Cardiol 7 2013 97 114
-
(2013)
Clin Med Insights Cardiol
, vol.7
, pp. 97-114
-
-
Romero, J.1
Mejia-Lopez, E.2
Manrique, C.3
-
30
-
-
84890228387
-
Sarcomeric gene causing DCM: Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy
-
M. Merlo, G. Sinagra, and E. Carniel et al. Sarcomeric gene causing DCM: poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy Clin Transl Sci 6 2013 424 428
-
(2013)
Clin Transl Sci
, vol.6
, pp. 424-428
-
-
Merlo, M.1
Sinagra, G.2
Carniel, E.3
-
31
-
-
82255162644
-
Desmosomal protein gene mutations in patients with idiopathic DCM
-
M. Zhang, F. Tavora, and A. Burke Desmosomal protein gene mutations in patients with idiopathic DCM Heart 97 2011 2090
-
(2011)
Heart
, vol.97
, pp. 2090
-
-
Zhang, M.1
Tavora, F.2
Burke, A.3
-
32
-
-
84860615370
-
Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy
-
G. Quarta, P. Syrris, and M. Ashworth et al. Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy Eur Heart J 33 2012 1128 1136
-
(2012)
Eur Heart J
, vol.33
, pp. 1128-1136
-
-
Quarta, G.1
Syrris, P.2
Ashworth, M.3
-
33
-
-
84864004251
-
Non sarcomeric genes cause HCM: Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy
-
F.W. Friedrich, B.R. Wilding, and S. Reischmann et al. Non sarcomeric genes cause HCM: evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy Hum Mol Genet 21 2012 3237 3254
-
(2012)
Hum Mol Genet
, vol.21
, pp. 3237-3254
-
-
Friedrich, F.W.1
Wilding, B.R.2
Reischmann, S.3
-
34
-
-
77949881591
-
Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations
-
F. Girolami, C.Y. Ho, and C. Semsarian et al. Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations J Am Coll Cardiol 55 2010 1444 1453
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 1444-1453
-
-
Girolami, F.1
Ho, C.Y.2
Semsarian, C.3
-
35
-
-
84883760401
-
New approaches to the clinical diagnosis of inherited heart muscle disease
-
L.R. Lopes, and P.M. Elliott New approaches to the clinical diagnosis of inherited heart muscle disease Heart 99 2013 1451 1461
-
(2013)
Heart
, vol.99
, pp. 1451-1461
-
-
Lopes, L.R.1
Elliott, P.M.2
-
36
-
-
84873724796
-
Genetic testing in the contemporary diagnosis of cardiomyopathy
-
A.C. Sturm Genetic testing in the contemporary diagnosis of cardiomyopathy Curr Heart Fail Rep 10 2013 63 72
-
(2013)
Curr Heart Fail Rep
, vol.10
, pp. 63-72
-
-
Sturm, A.C.1
-
37
-
-
84877762969
-
Genetic evaluation of dilated cardiomyopathy
-
A. Morales, and R.E. Hershberger Genetic evaluation of dilated cardiomyopathy Curr Cardiol Rep 15 2013 375
-
(2013)
Curr Cardiol Rep
, vol.15
, pp. 375
-
-
Morales, A.1
Hershberger, R.E.2
-
38
-
-
84888027867
-
Next-generation sequencing: From understanding biology to personalized medicine
-
K.S. Frese, H.A. Katus, and B. Meder Next-generation sequencing: from understanding biology to personalized medicine Biology 2 2013 378 398
-
(2013)
Biology
, vol.2
, pp. 378-398
-
-
Frese, K.S.1
Katus, H.A.2
Meder, B.3
-
39
-
-
26444535644
-
Is it time to include ion channel diseases among cardiomyopathies?
-
D. Corrado, C. Basso, and G. Thiene Is it time to include ion channel diseases among cardiomyopathies? J Electrocardiol 38 Suppl 4 2005 81 87
-
(2005)
J Electrocardiol
, vol.38
, Issue.SUPPL. 4
, pp. 81-87
-
-
Corrado, D.1
Basso, C.2
Thiene, G.3
-
40
-
-
63049090664
-
Classification of cardiomyopathies and indication for endomyocardial biopsy revisited
-
S. Pankuweit, A. Richter, and V. Ruppert et al. Classification of cardiomyopathies and indication for endomyocardial biopsy revisited Herz 34 2009 55 62
-
(2009)
Herz
, vol.34
, pp. 55-62
-
-
Pankuweit, S.1
Richter, A.2
Ruppert, V.3
-
41
-
-
84872089353
-
An update on channelopathies: From mechanisms to management
-
G. Webster, and C.I. Berul An update on channelopathies: from mechanisms to management Circulation 127 2013 126 140
-
(2013)
Circulation
, vol.127
, pp. 126-140
-
-
Webster, G.1
Berul, C.I.2
-
42
-
-
84860390502
-
Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects
-
M. Diegoli, M. Grasso, and V. Favalli et al. Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects J Am Coll Cardiol 58 2011 925 934
-
(2011)
J Am Coll Cardiol
, vol.58
, pp. 925-934
-
-
Diegoli, M.1
Grasso, M.2
Favalli, V.3
-
43
-
-
52949111684
-
Long-term outcome and risk stratification in dilated cardiolaminopathies
-
M. Pasotti, C. Klersy, and A. Pilotto et al. Long-term outcome and risk stratification in dilated cardiolaminopathies J Am Coll Cardiol 52 2008 1250 1260
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 1250-1260
-
-
Pasotti, M.1
Klersy, C.2
Pilotto, A.3
-
44
-
-
61349154811
-
Differential involvement of sarcomeric proteins in myofibrillar myopathies: A morphological and immunohistochemical study
-
K.G. Claeys, P.F. van der Ven, and A. Behin et al. Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Acta Neuropathol 117 2009 293 307
-
(2009)
Acta Neuropathol
, vol.117
, pp. 293-307
-
-
Claeys, K.G.1
Van Der Ven, P.F.2
Behin, A.3
-
45
-
-
79955527259
-
Analysis of myotilin turnover provides mechanistic insight into the role of myotilinopathy-causing mutations
-
P. von Nandelstadh, R. Soliymani, and M. Baumann et al. Analysis of myotilin turnover provides mechanistic insight into the role of myotilinopathy-causing mutations Biochem J 436 2011 113 121
-
(2011)
Biochem J
, vol.436
, pp. 113-121
-
-
Von Nandelstadh, P.1
Soliymani, R.2
Baumann, M.3
-
46
-
-
84872374881
-
The medical genetics of dystrophinopathies: Molecular genetic diagnosis and its impact on clinical practice
-
A. Ferlini, M. Neri, and F. Gualandi The medical genetics of dystrophinopathies: molecular genetic diagnosis and its impact on clinical practice Neuromuscul Disord 23 2013 4
-
(2013)
Neuromuscul Disord
, vol.23
, pp. 4
-
-
Ferlini, A.1
Neri, M.2
Gualandi, F.3
-
48
-
-
84877817701
-
Caveolinopathies
-
R.A. Pagon, T.D. Bird, C.R. Dolan, K. Stephens, M.P. Adam, University of Washington Seattle Seattle, WA
-
C. Bruno, F. Sotgia, and E. Gazzerro et al. Caveolinopathies R.A. Pagon, T.D. Bird, C.R. Dolan, K. Stephens, M.P. Adam, GeneReviews. [Internet] 2012 University of Washington Seattle Seattle, WA
-
(2012)
GeneReviews. [Internet]
-
-
Bruno, C.1
Sotgia, F.2
Gazzerro, E.3
-
49
-
-
38749153262
-
Limb-girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis
-
H.P. Lo, S.T. Cooper, and F.J. Evesson et al. Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis Neuromuscul Disord 18 2008 34 44
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 34-44
-
-
Lo, H.P.1
Cooper, S.T.2
Evesson, F.J.3
-
50
-
-
84897595312
-
D. Myoglobinuria as first clinical sign of a primary alpha- sarcoglycanopathy
-
F. Ceravolo, S. Messina, and C. Rodolico et al. D. Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathy Eur J Pediatr 173 2014 239 242
-
(2014)
Eur J Pediatr
, vol.173
, pp. 239-242
-
-
Ceravolo, F.1
Messina, S.2
Rodolico, C.3
-
51
-
-
84873573109
-
Treatment of dysferlinopathy with deflazacort: A double-blind, placebo-controlled clinical trial
-
M.C. Walter, P. Reilich, and S. Thiele et al. Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial Orphanet J Rare Dis 8 2013 26
-
(2013)
Orphanet J Rare Dis
, vol.8
, pp. 26
-
-
Walter, M.C.1
Reilich, P.2
Thiele, S.3
-
52
-
-
0030499025
-
HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies
-
E.P. Hoffman, and P.R. Clemens HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies Curr Opin Rheumatol 8 1996 528 538
-
(1996)
Curr Opin Rheumatol
, vol.8
, pp. 528-538
-
-
Hoffman, E.P.1
Clemens, P.R.2
-
54
-
-
84888331101
-
The MOGE(S) Classification for a phenotype-genotype nomenclature of cardiomyopathy. Endorsed by the World Heart Federation
-
E. Arbustini, N. Narula, and W.G. Dec et al. The MOGE(S) Classification for a phenotype-genotype nomenclature of cardiomyopathy. Endorsed by the World Heart Federation J Am Coll Cardiol 62 2013 2046 2072
-
(2013)
J Am Coll Cardiol
, vol.62
, pp. 2046-2072
-
-
Arbustini, E.1
Narula, N.2
Dec, W.G.3
-
55
-
-
84892719590
-
The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy. Endorsed by the World Heart Federation
-
E. Arbustini, N. Narula, and W.G. Dec et al. The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy. endorsed by the World Heart Federation G Heart 8 2013 355 382
-
(2013)
G Heart
, vol.8
, pp. 355-382
-
-
Arbustini, E.1
Narula, N.2
Dec, W.G.3
-
57
-
-
84904582040
-
-
Human Genome Variation Society. Accessed June 5, 2014
-
Human Genome Variation Society. Available at: http://www.hgvs.org/ mutnomen/. Accessed June 5, 2014.
-
-
-
-
58
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
I.A. Adzhubei, S. Schmidt, and L. Peshkin et al. A method and server for predicting damaging missense mutations Nat Methods 7 2010 248 249
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
-
59
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
P. Kumar, S. Henikoff, and P.C. Ng Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm Nat Protoc 4 2009 1073 1081
-
(2009)
Nat Protoc
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
60
-
-
84862648756
-
-
National Heart, Lung, and Blood Institute Accessed June 5, 2014
-
National Heart, Lung, and Blood Institute. Exome Sequencing Project. Hosted by the University of Washington. Available at: http://evs.gs.washington. edu/EVS/. Accessed June 5, 2014.
-
Exome Sequencing Project. Hosted by the University of Washington
-
-
-
61
-
-
84904549206
-
-
1,000 Genome Project. Accessed June 5, 2014
-
1,000 Genome Project. Available at: http://www.1000genomes.org/about. Accessed June 5, 2014.
-
-
-
-
62
-
-
84904577438
-
-
Universal Mutation Database. Accessed June 5, 2014
-
Universal Mutation Database. Available at: http://www.umd.be/HSF/. Accessed June 5, 2014.
-
-
-
-
63
-
-
84904571000
-
-
MOGES. Accessed June 5, 2014
-
MOGES. Available at: http://moges.biomeris.com/. Accessed June 5, 2014.
-
-
-
-
64
-
-
84899643722
-
MOGE(S) nosology in low-to-middle-income countries
-
E. Arbustini, N. Narula, and G.W. Dec et al. MOGE(S) nosology in low-to-middle-income countries Nat Rev Cardiol 11 2014 307
-
(2014)
Nat Rev Cardiol
, vol.11
, pp. 307
-
-
Arbustini, E.1
Narula, N.2
Dec, G.W.3
-
65
-
-
84876260987
-
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy
-
C. Brodt, J.D. Siegfried, and M. Hofmeyer et al. Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy J Card Fail 19 2013 233 239
-
(2013)
J Card Fail
, vol.19
, pp. 233-239
-
-
Brodt, C.1
Siegfried, J.D.2
Hofmeyer, M.3
-
66
-
-
84888348316
-
Classification of cardiomyopathies: Evolution or revolution?
-
P.M. Elliott Classification of cardiomyopathies: evolution or revolution? J Am Coll Cardiol 62 2013 2073 2074
-
(2013)
J Am Coll Cardiol
, vol.62
, pp. 2073-2074
-
-
Elliott, P.M.1
-
67
-
-
84896717733
-
Cardiomyopathies: MOGE(S): A standardized classification of cardiomyopathies?
-
B.M. Mayosi Cardiomyopathies: MOGE(S): a standardized classification of cardiomyopathies? Nat Rev Cardiol 11 2014 134 135
-
(2014)
Nat Rev Cardiol
, vol.11
, pp. 134-135
-
-
Mayosi, B.M.1
-
68
-
-
77950482741
-
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed modification of the Task Force Criteria
-
F.I. Marcus, W.J. McKenna, and D. Sherrill et al. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria Eur Heart J 31 2010 806 814
-
(2010)
Eur Heart J
, vol.31
, pp. 806-814
-
-
Marcus, F.I.1
McKenna, W.J.2
Sherrill, D.3
-
69
-
-
84902161337
-
The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy: More questions than answers?
-
(letter)
-
E. Arbustini, N. Narula, and W.G. Dec et al. The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy: more questions than answers? (letter) J Am Coll Cardiol 63 2014 2584 2586
-
(2014)
J Am Coll Cardiol
, vol.63
, pp. 2584-2586
-
-
Arbustini, E.1
Narula, N.2
Dec, W.G.3
-
70
-
-
77950861130
-
Forgotten cardiovascular diseases in Africa
-
K. Sliwa, and A.O. Mocumbi Forgotten cardiovascular diseases in Africa Clin Res Cardiol 99 2010 65 74
-
(2010)
Clin Res Cardiol
, vol.99
, pp. 65-74
-
-
Sliwa, K.1
Mocumbi, A.O.2
-
71
-
-
0007549656
-
Myocarditis and myocardosis: A clinicopathologic appraisal
-
M.A. Blankerhorn, and E.A. Gall Myocarditis and myocardosis: a clinicopathologic appraisal Circulation 13 1956 217 223
-
(1956)
Circulation
, vol.13
, pp. 217-223
-
-
Blankerhorn, M.A.1
Gall, E.A.2
-
72
-
-
0000591152
-
Uncommon myocardial diseases: The non-coronary cardiomyopathies
-
W. Bridgen Uncommon myocardial diseases: the non-coronary cardiomyopathies Lancet 273 1957 1179 1184
-
(1957)
Lancet
, vol.273
, pp. 1179-1184
-
-
Bridgen, W.1
-
74
-
-
0019205841
-
Report of the WHO/ISFC Task Force on the definition and classification of cardiomyopathies
-
Report of the WHO/ISFC Task Force on the definition and classification of cardiomyopathies Br Heart J 44 1980 672 673
-
(1980)
Br Heart J
, vol.44
, pp. 672-673
-
-
-
75
-
-
0029864693
-
Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies
-
P. Richardson, W. McKenna, and M. Bristow et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies Circulation 93 1996 841 842
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
Richardson, P.1
McKenna, W.2
Bristow, M.3
-
76
-
-
60949103027
-
Heart Failure Society of America. Genetic evaluation of cardiomyopathy - A Heart Failure Society of America practice guideline
-
R.E. Hershberger, J. Lindenfeld, L. Mestroni, C.E. Seidman, M.R. Taylor, and J.A. Towbin et al. Heart Failure Society of America. Genetic evaluation of cardiomyopathy - a Heart Failure Society of America practice guideline J Cardiol Fail 15 2009 83 97
-
(2009)
J Cardiol Fail
, vol.15
, pp. 83-97
-
-
Hershberger, R.E.1
Lindenfeld, J.2
Mestroni, L.3
Seidman, C.E.4
Taylor, M.R.5
Towbin, J.A.6
-
77
-
-
80051710052
-
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
-
M.J. Ackerman, S.G. Priori, and S. Willems et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) Europace 13 2011 1077 1109
-
(2011)
Europace
, vol.13
, pp. 1077-1109
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
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