메뉴 건너뛰기




Volumn 12, Issue 6, 2010, Pages 598-613

Arrhythmogenic right ventricular dysplasia

Author keywords

[No Author keywords available]

Indexed keywords

AMIODARONE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CADHERIN; DESMOCOLLIN; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; PLAKOGLOBIN; PLAKOPHILIN; SOTALOL;

EID: 78649909066     PISSN: 10928464     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11936-010-0097-2     Document Type: Review
Times cited : (6)

References (53)
  • 1
    • 0020077022 scopus 로고
    • Right ventricular dysplasia: A report of 24 adult cases
    • F Marcus G Fontaine G Guiraudon, et al. 1982 Right ventricular dysplasia: a report of 24 adult cases Circulation 65 384 398 1:STN:280: DyaL38%2FptlOluw%3D%3D 7053899 (Pubitemid 12219036)
    • (1982) Circulation , vol.65 , Issue.2 , pp. 384-398
    • Marcus, F.I.1    Fontaine, G.H.2    Guiraudon, G.3
  • 2
    • 0032939409 scopus 로고    scopus 로고
    • Cardiovascular causes of sudden death in young individuals including athletes
    • 1:STN:280:DyaK1MzlsVWrug%3D%3D 10.1097/00045415-199905000-00009 10423663
    • C Basso D Corrado G Thiene 1999 Cardiovascular causes of sudden death in young individuals including athletes Cardiol Rev 7 127 135 1:STN:280: DyaK1MzlsVWrug%3D%3D 10.1097/00045415-199905000-00009 10423663
    • (1999) Cardiol Rev , vol.7 , pp. 127-135
    • Basso, C.1    Corrado, D.2    Thiene, G.3
  • 3
    • 9244247300 scopus 로고    scopus 로고
    • Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital
    • DOI 10.1016/j.ijcard.2003.10.037, PII S016752730400049X
    • S Peters M Trummel W Meyners 2004 Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital Int J Cardiol 97 499 501 10.1016/j.ijcard.2003.10.037 15561339 (Pubitemid 39550701)
    • (2004) International Journal of Cardiology , vol.97 , Issue.3 , pp. 499-501
    • Peters, S.1    Trummel, M.2    Meyners, W.3
  • 4
    • 33750569831 scopus 로고    scopus 로고
    • The mystery of arrhythmogenic right ventricular dysplasia/cardiomyopathy: From observation to mechanistic explanation
    • DOI 10.1161/CIRCULATIONAHA.106.653493, PII 0000301720061024000003
    • F Marcus JA Towbin 2006 The mystery of arrhythmogenic right ventricular dysplasia/cardiomyopathy: from observation to mechanistic explanation Circulation 114 1794 1795 10.1161/CIRCULATIONAHA.106.653493 17060394 (Pubitemid 44673352)
    • (2006) Circulation , vol.114 , Issue.17 , pp. 1794-1795
    • Marcus, F.1    Towbin, J.A.2
  • 7
    • 14244250082 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy: Clinical presentation, diagnosis, and management
    • DOI 10.1016/j.amjmed.2004.04.028
    • S Sen-Chowdhry MD Lowe SC Sporton, et al. 2004 Arrhythmogenic right ventricular cardiomyopathy: clinical presentation, diagnosis, and management Am J Med 117 685 695 10.1016/j.amjmed.2004.04.028 15501207 (Pubitemid 40288176)
    • (2004) American Journal of Medicine , vol.117 , Issue.9 , pp. 685-695
    • Sen-Chowdhry, S.1    Lowe, M.D.2    Sporton, S.C.3    McKenna, W.J.4
  • 8
    • 34247280500 scopus 로고    scopus 로고
    • Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression
    • DOI 10.1161/CIRCULATIONAHA.106.660241
    • S Sen-Chowdhry P Syrris D Ward, et al. 2007 Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression Circulation 115 1710 1720 10.1161/CIRCULATIONAHA.106.660241 17372169 (Pubitemid 46648607)
    • (2007) Circulation , vol.115 , Issue.13 , pp. 1710-1720
    • Sen-Chowdhry, S.1    Syrris, P.2    Ward, D.3    Asimaki, A.4    Sevdalis, E.5    McKenna, W.J.6
  • 9
    • 63549109935 scopus 로고    scopus 로고
    • Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • 10.1016/j.jacc.2008.12.045 19358943 This genotype-MRI correlation study reported that in family members of ARVD probands, LV function is generally preserved and independent LV disease occurs rarely. It also showed the CMR features, such as the accordion sign, may be able to accurately detect early disease in affected family members.
    • D Dalal H Tandri D Judge, et al. 2009 Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy J Am Coll Cardiol 53 1289 1299 10.1016/j.jacc.2008.12.045 19358943 This genotype-MRI correlation study reported that in family members of ARVD probands, LV function is generally preserved and independent LV disease occurs rarely. It also showed the CMR features, such as the accordion sign, may be able to accurately detect early disease in affected family members.
    • (2009) J Am Coll Cardiol , vol.53 , pp. 1289-1299
    • Dalal, D.1    Tandri, H.2    Judge, D.3
  • 10
    • 0029787576 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis?
    • 1:STN:280:DyaK28zot1WksA%3D%3D 8790036
    • C Basso G Thiene D Corrado, et al. 1996 Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis? Circulation 94 983 991 1:STN:280:DyaK28zot1WksA%3D%3D 8790036
    • (1996) Circulation , vol.94 , pp. 983-991
    • Basso, C.1    Thiene, G.2    Corrado, D.3
  • 11
    • 0032574651 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium: Are they different diseases?
    • 1:STN:280:DyaK1c3lsVeqtg%3D%3D 9593562
    • AP Burke A Farb G Tashko, et al. 1998 Arrhythmogenic right ventricular cardiomyopathy and fatty replacement of the right ventricular myocardium: are they different diseases? Circulation 97 1571 1580 1:STN:280:DyaK1c3lsVeqtg%3D%3D 9593562
    • (1998) Circulation , vol.97 , pp. 1571-1580
    • Burke, A.P.1    Farb, A.2    Tashko, G.3
  • 12
    • 17444438135 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular dysplasia/cardiomyopathy. Need for an international registry
    • D Corrado G Fontaine FI Marcus, et al. 2000 Arrhythmogenic right ventricular dysplasia/cardiomyopathy. Need for an international registry Circulation 101 101 106
    • (2000) Circulation , vol.101 , pp. 101-106
    • Corrado, D.1    Fontaine, G.2    Marcus, F.I.3
  • 13
    • 0034679297 scopus 로고    scopus 로고
    • Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
    • 1:CAS:528:DC%2BD3cXkvVWjtrg%3D 10.1016/S0140-6736(00)02379-5 10902626
    • G McKoy N Protonotarios A Crosby, et al. 2000 Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease) Lancet 355 2119 2124 1:CAS:528:DC%2BD3cXkvVWjtrg%3D 10.1016/S0140-6736(00)02379-5 10902626
    • (2000) Lancet , vol.355 , pp. 2119-2124
    • McKoy, G.1    Protonotarios, N.2    Crosby, A.3
  • 14
    • 0034326902 scopus 로고    scopus 로고
    • Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma
    • 1:CAS:528:DC%2BD3cXosVKkur4%3D 10.1093/hmg/9.18.2761 11063735
    • EE Norgett SJ Hatsell L Carvajal-Huerta, et al. 2000 Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma Hum Mol Genet 9 2761 2766 1:CAS:528:DC%2BD3cXosVKkur4%3D 10.1093/hmg/9.18.2761 11063735
    • (2000) Hum Mol Genet , vol.9 , pp. 2761-2766
    • Norgett, E.E.1    Hatsell, S.J.2    Carvajal-Huerta, L.3
  • 16
    • 33645527574 scopus 로고    scopus 로고
    • Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy
    • 1:CAS:528:DC%2BD28XhvVekt78%3D 10.1161/CIRCULATIONAHA.105.583674 16505173
    • K Pilichou A Nava C Basso, et al. 2006 Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy Circulation 113 1171 1179 1:CAS:528:DC%2BD28XhvVekt78%3D 10.1161/CIRCULATIONAHA.105.583674 16505173
    • (2006) Circulation , vol.113 , pp. 1171-1179
    • Pilichou, K.1    Nava, A.2    Basso, C.3
  • 17
    • 38049150175 scopus 로고    scopus 로고
    • Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
    • 10.1186/1471-2350-8-65 17963498
    • G Beffagna M De Bortoli A Nava, et al. 2007 Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro BMC Med Genet 8 65 10.1186/1471-2350-8-65 17963498
    • (2007) BMC Med Genet , vol.8 , pp. 65
    • Beffagna, G.1    De Bortoli, M.2    Nava, A.3
  • 20
    • 0035253502 scopus 로고    scopus 로고
    • Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
    • 1:CAS:528:DC%2BD3MXht1Sktb8%3D 10.1093/hmg/10.3.189 11159936
    • N Tiso DA Stephan A Nava, et al. 2001 Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) Hum Mol Genet 10 189 194 1:CAS:528:DC%2BD3MXht1Sktb8%3D 10.1093/hmg/10.3.189 11159936
    • (2001) Hum Mol Genet , vol.10 , pp. 189-194
    • Tiso, N.1    Stephan, D.A.2    Nava, A.3
  • 21
    • 41649107651 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene
    • 10.1016/j.ajhg.2008.01.010 This article showed that mutation in a non-desmosomal protein is associated with a subtype of ARVD with prominent left ventricular disease.
    • ND Merner KA Hodgkinson AFM Haywood, et al. 2008 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 82 1 13 10.1016/j.ajhg.2008.01.010 This article showed that mutation in a non-desmosomal protein is associated with a subtype of ARVD with prominent left ventricular disease.
    • (2008) Am J Hum Genet , vol.82 , pp. 1-13
    • Merner, N.D.1    Hodgkinson, K.A.2    Haywood, A.F.M.3
  • 22
    • 77949908549 scopus 로고    scopus 로고
    • Comprehensive desmosome mutation analysis in North Americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • 10.1161/CIRCGENETICS.109.858217 This was the first study to evaluate the prevalence and significance of desmosomal protein mutations in North Americans with known ARVD. It also highlighted that fact that despite recent advances in our understanding of the genetic basis of this disease, as many as 50% of ARVD patients still have no identifiable mutation.
    • A den Haan B Tan M Zikusoka, et al. 2009 Comprehensive desmosome mutation analysis in North Americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy Circ Cardiovasc Genet 2 428 435 10.1161/CIRCGENETICS. 109.858217 This was the first study to evaluate the prevalence and significance of desmosomal protein mutations in North Americans with known ARVD. It also highlighted that fact that despite recent advances in our understanding of the genetic basis of this disease, as many as 50% of ARVD patients still have no identifiable mutation.
    • (2009) Circ Cardiovasc Genet , vol.2 , pp. 428-435
    • Den Haan, A.1    Tan, B.2    Zikusoka, M.3
  • 23
    • 2942726109 scopus 로고    scopus 로고
    • Naxos disease and Carvajal syndrome: Cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy
    • DOI 10.1016/j.carpath.2004.03.609, PII S105488070400657X
    • N Protonotarios A Tsatsopoulou 2004 Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy Cardiovasc Pathol 13 185 194 1:CAS:528:DC%2BD2cXltVCqtbk%3D 10.1016/j.carpath.2004.03.609 15210133 (Pubitemid 38798357)
    • (2004) Cardiovascular Pathology , vol.13 , Issue.4 , pp. 185-194
    • Protonotarios, N.1    Tsatsopoulou, A.2
  • 24
  • 26
    • 55449109130 scopus 로고    scopus 로고
    • Gap junction remodeling in a case of arrhythmogenic right ventricular dysplasia due to plakoglobin-2 mutation
    • 10.1111/j.1540-8167.2008.01207.x
    • H Tandri A Asimaki D Dalal, et al. 2008 Gap junction remodeling in a case of arrhythmogenic right ventricular dysplasia due to plakoglobin-2 mutation J Cardiovasc Electrophysiol 11 1212 1214 10.1111/j.1540-8167.2008.01207.x
    • (2008) J Cardiovasc Electrophysiol , vol.11 , pp. 1212-1214
    • Tandri, H.1    Asimaki, A.2    Dalal, D.3
  • 28
    • 33745848407 scopus 로고    scopus 로고
    • Suppression of canonical Wnt/β-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy
    • DOI 10.1172/JCI27751
    • E Garcia-Gras R Lombardi MJ Giocondo, et al. 2006 Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy J Clin Invest 116 2012 2021 1:CAS:528:DC%2BD28XmvV2lu74%3D 10.1172/JCI27751 16823493 (Pubitemid 44033325)
    • (2006) Journal of Clinical Investigation , vol.116 , Issue.7 , pp. 2012-2021
    • Garcia-Gras, E.1    Lombardi, R.2    Giocondo, M.J.3    Willerson, J.T.4    Schneider, M.D.5    Khoury, D.S.6    Marian, A.J.7
  • 30
    • 75249083039 scopus 로고    scopus 로고
    • Compound and digenic hetrozygosity contributes to arrhythmogenic right ventricular cardiomyopathy
    • 1:CAS:528:DC%2BC3cXjt1Gmsrs%3D 10.1016/j.jacc.2009.11.020 20152563 This study showed that ARVD patients often display compound and digenic heterozygosity for desmosomal protein mutations. It provided support for the "second hit" hypothesis and showed that compound/digenic heterozygosity may be a potential mechanism of the variability in penetrance and expressivity of this disease. It also highlighted the complexity of using genetic analysis to diagnose ARVD.
    • T Xu Z Yang M Vatta, et al. 2010 Compound and digenic hetrozygosity contributes to arrhythmogenic right ventricular cardiomyopathy J Am Coll Cardiol 55 587 597 1:CAS:528:DC%2BC3cXjt1Gmsrs%3D 10.1016/j.jacc.2009.11.020 20152563 This study showed that ARVD patients often display compound and digenic heterozygosity for desmosomal protein mutations. It provided support for the "second hit" hypothesis and showed that compound/digenic heterozygosity may be a potential mechanism of the variability in penetrance and expressivity of this disease. It also highlighted the complexity of using genetic analysis to diagnose ARVD.
    • (2010) J Am Coll Cardiol , vol.55 , pp. 587-597
    • Xu, T.1    Yang, Z.2    Vatta, M.3
  • 31
    • 0037028908 scopus 로고    scopus 로고
    • The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • DOI 10.1016/S0735-1097(02)01688-1, PII S0735109702016881
    • NE Bowles J Ni F Marcus, et al. 2002 The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy J Am Coll Cardiol 39 892 895 10.1016/S0735-1097(02) 01688-1 11869858 (Pubitemid 34185340)
    • (2002) Journal of the American College of Cardiology , vol.39 , Issue.5 , pp. 892-895
    • Bowles, N.E.1    Ni, J.2    Marcus, F.3    Towbin, J.A.4
  • 34
    • 20844436916 scopus 로고    scopus 로고
    • Electrocardiographic features of arrhythmogenic right ventricular dysplasia/cardiomyopathy according to disease severity: A need to broaden diagnostic criteria
    • DOI 10.1161/01.CIR.0000142293.60725.18
    • K Nasir C Bomma H Tandri, et al. 2004 Electrocardiographic features of arrhythmogenic right ventricular dysplasia/cardiomyopathy according to disease severity: a need to broaden diagnostic criteria Circulation 110 1527 1534 10.1161/01.CIR.0000142293.60725.18 15381658 (Pubitemid 39297972)
    • (2004) Circulation , vol.110 , Issue.12 , pp. 1527-1534
    • Nasir, K.1    Bomma, C.2    Tandri, H.3    Roguin, A.4    Dalal, D.5    Prakasa, K.6    Tichnell, C.7    James, C.8    Jspevak, P.9    Marcus, F.10    Calkins, H.11
  • 35
    • 75249096712 scopus 로고    scopus 로고
    • Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed modification of the Task Force Criteria
    • 10.1161/CIRCULATIONAHA.108.840827 20172911 This article provided a new model for the diagnosis of ARVD. It eliminated the subjectivity of many of the original Task Force criteria (such as for ventricular structure and function) by introducing validated imaging parameters. It also incorporated recently acquired knowledge and new technologies (such as CMR and genetic testing) to improve diagnostic sensitivity.
    • F Marcus W McKenna D Sherrill, et al. 2010 Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria Circulation 121 1533 1541 10.1161/CIRCULATIONAHA.108.840827 20172911 This article provided a new model for the diagnosis of ARVD. It eliminated the subjectivity of many of the original Task Force criteria (such as for ventricular structure and function) by introducing validated imaging parameters. It also incorporated recently acquired knowledge and new technologies (such as CMR and genetic testing) to improve diagnostic sensitivity.
    • (2010) Circulation , vol.121 , pp. 1533-1541
    • Marcus, F.1    McKenna, W.2    Sherrill, D.3
  • 37
    • 69449098428 scopus 로고    scopus 로고
    • Electrocardiographic features of arrhythmogenic right ventricular dysplasia
    • 10.1161/CIRCULATIONAHA.108.838821 19635971 This study evaluated the sensitivity and specificity of some of the various ECG features of ARVD in the presence and absence of RBBB.
    • R Jain D Dalal A Daly, et al. 2009 Electrocardiographic features of arrhythmogenic right ventricular dysplasia Circulation 120 477 487 10.1161/CIRCULATIONAHA.108.838821 19635971 This study evaluated the sensitivity and specificity of some of the various ECG features of ARVD in the presence and absence of RBBB.
    • (2009) Circulation , vol.120 , pp. 477-487
    • Jain, R.1    Dalal, D.2    Daly, A.3
  • 38
    • 14844303915 scopus 로고    scopus 로고
    • Echocardiographic findings in patients meeting task force criteria for arrhythmogenic right ventricular dysplasia: New insights from the multidisciplinary study of right ventricular dysplasia
    • DOI 10.1016/j.jacc.2004.10.070
    • DM Yoerger F Marcus D Sherrill, et al. 2005 Echocardiographic findings in patients meeting task force criteria for arrhythmogenic right ventricular dysplasia: new insights from the multidisciplinary study of right ventricular dysplasia J Am Coll Cardiol 45 860 865 10.1016/j.jacc.2004.10.070 15766820 (Pubitemid 40342810)
    • (2005) Journal of the American College of Cardiology , vol.45 , Issue.6 , pp. 860-865
    • Yoerger, D.M.1    Marcus, F.2    Sherrill, D.3    Calkins, H.4    Towbin, J.A.5    Zareba, W.6    Picard, M.H.7
  • 40
    • 13844250348 scopus 로고    scopus 로고
    • Adipositas cordis, fatty infiltration of the right ventricle, and arrhythmogenic right ventricular cardiomyopathy. Just a matter of fat?
    • DOI 10.1016/j.carpath.2004.12.001
    • C Basso G Thiene 2005 Adipositas cordis, fatty infiltration of the right ventricle, and arrhythmogenic right ventricular cardiomyopathy. Just a matter of fat? Cardiovasc Pathol 14 37 41 10.1016/j.carpath.2004.12.001 15710290 (Pubitemid 40248431)
    • (2005) Cardiovascular Pathology , vol.14 , Issue.1 , pp. 37-41
    • Basso, C.1    Thiene, G.2
  • 41
    • 67549116786 scopus 로고    scopus 로고
    • Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: Results from the North American Multidisciplinary Study
    • 10.1016/j.hrthm.2009.03.013 19560088 This study described the clinical profile of a large group of ARVD patients in North America. It reported the relative utility (including the sensitivity and specificity) of the various diagnostic tests used for the evaluation of ARVD patients. It also highlighted the complexities of diagnosing ARVD.
    • F Marcus W Zareba H Calkins, et al. 2009 Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: Results from the North American Multidisciplinary Study Heart Rhythm 6 984 992 10.1016/j.hrthm.2009.03.013 19560088 This study described the clinical profile of a large group of ARVD patients in North America. It reported the relative utility (including the sensitivity and specificity) of the various diagnostic tests used for the evaluation of ARVD patients. It also highlighted the complexities of diagnosing ARVD.
    • (2009) Heart Rhythm , vol.6 , pp. 984-992
    • Marcus, F.1    Zareba, W.2    Calkins, H.3
  • 44
    • 62349094053 scopus 로고    scopus 로고
    • A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy
    • 1:CAS:528:DC%2BD1MXjtFyisL0%3D 10.1056/NEJMoa0808138 19279339 This study described a new diagnostic test for ARVD. It showed that immunohistochemical analysis of tissue specimens can provide high diagnostic sensitivity and specificity and improve the utility of endomyocardial biopsy.
    • A Asimaki H Tandri H Huang, et al. 2009 A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy N Engl J Med 360 1075 1084 1:CAS:528:DC%2BD1MXjtFyisL0%3D 10.1056/NEJMoa0808138 19279339 This study described a new diagnostic test for ARVD. It showed that immunohistochemical analysis of tissue specimens can provide high diagnostic sensitivity and specificity and improve the utility of endomyocardial biopsy.
    • (2009) N Engl J Med , vol.360 , pp. 1075-1084
    • Asimaki, A.1    Tandri, H.2    Huang, H.3
  • 45
    • 0028347223 scopus 로고
    • 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
    • 1:STN:280:DyaK2c7ptVKrtg%3D%3D 10.1136/hrt.71.3.215 8142187
    • W McKenna G Thiene A Nava, et al. 1994 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 71 215 218 1:STN:280:DyaK2c7ptVKrtg%3D%3D 10.1136/hrt.71.3.215 8142187
    • (1994) Br Heart J , vol.71 , pp. 215-218
    • McKenna, W.1    Thiene, G.2    Nava, A.3
  • 51
    • 34247113286 scopus 로고    scopus 로고
    • Radiofrequency ablation of the ventricular tachycardia with arrhythmogenic right ventricular cardiomyopathy using non-contact mapping
    • DOI 10.1111/j.1540-8159.2007.00703.x
    • Y Yao S Zhang D Sheng, et al. 2007 Radiofrequency ablation of the ventricular tachycardia with arrhythmogenic right ventricular cardiomyopathy using non-contact mapping Pacing Clin Electrophysiol 30 526 533 10.1111/j.1540-8159.2007.00703.x 17437577 (Pubitemid 46596130)
    • (2007) PACE - Pacing and Clinical Electrophysiology , vol.30 , Issue.4 , pp. 526-533
    • Yao, Y.1    Zhang, S.2    He, D.S.3    Zhang, K.4    Hua, W.5    Chu, J.6    Pu, J.7    Chen, K.8    Wang, F.9    Chen, X.10
  • 52
    • 67849085428 scopus 로고    scopus 로고
    • Efficacy of antiarrhythmic drugs in arrhythmogenic right ventricular cardiomyopathy: A report from the North American ARVC Registry
    • 1:CAS:528:DC%2BD1MXhtFaksbjI 10.1016/j.jacc.2009.04.052 19660690
    • G Marcus D Glidden B Polonsky, et al. 2009 Efficacy of antiarrhythmic drugs in arrhythmogenic right ventricular cardiomyopathy: a report from the North American ARVC Registry J Am Coll Cardiol 54 609 615 1:CAS:528: DC%2BD1MXhtFaksbjI 10.1016/j.jacc.2009.04.052 19660690
    • (2009) J Am Coll Cardiol , vol.54 , pp. 609-615
    • Marcus, G.1    Glidden, D.2    Polonsky, B.3
  • 53
    • 35548997132 scopus 로고    scopus 로고
    • Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • DOI 10.1016/j.jacc.2007.08.008, PII S0735109707026496
    • S Sen-Chowdhry P Syrris WJ McKenna 2007 Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy J Am Coll Cardiol 50 1813 1821 1:CAS:528: DC%2BD2sXht1Glur%2FL 10.1016/j.jacc.2007.08.008 17980246 (Pubitemid 350007965)
    • (2007) Journal of the American College of Cardiology , vol.50 , Issue.19 , pp. 1813-1821
    • Sen-Chowdhry, S.1    Syrris, P.2    McKenna, W.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.