Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
暂无分享,去创建一个
[1] G. Mönnig,et al. Risk stratification in arrhythmogenic right ventricular cardiomyopathy , 2013, Herzschrittmachertherapie + Elektrophysiologie.
[2] M. Komajda,et al. Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia. , 2013, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.
[3] A. Schinkel. Implantable Cardioverter Defibrillators in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Patient Outcomes, Incidence of Appropriate and Inappropriate Interventions, and Complications , 2013, Circulation. Arrhythmia and electrophysiology.
[4] P. Elliott,et al. Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada. , 2013, European heart journal.
[5] V. Pascali,et al. Genetics of arrhythmogenic right ventricular cardiomyopathy , 2013, Journal of Medical Genetics.
[6] R. Lucariello,et al. Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review , 2013, Clinical Medicine Insights. Cardiology.
[7] C. Stefanadis,et al. Myocardial mechanics for the early detection of cardiac sarcoidosis. , 2012, International journal of cardiology.
[8] E. Fabris,et al. The Role of Clinical Observation: Red Flag 5 — Right Ventricular Involvement, Arrhythmogenic Right Ventricular Cardiomyopathy and Associated Phenotypes , 2013 .
[9] L. Mestroni,et al. Utility of cardiac magnetic resonance imaging to differentiate cardiac sarcoidosis from arrhythmogenic right ventricular cardiomyopathy. , 2012, The American journal of cardiology.
[10] M. Ashworth,et al. Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy. , 2012, European heart journal.
[11] B. Murray. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Review of Molecular and Clinical Literature , 2012, Journal of Genetic Counseling.
[12] S. Russell,et al. Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention. , 2011, Journal of the American College of Cardiology.
[13] Brian R. Anderson,et al. Genetic Variation in Titin in Arrhythmogenic Right Ventricular Cardiomyopathy–Overlap Syndromes , 2011, Circulation.
[14] L. Mestroni,et al. Prognostic predictors in arrhythmogenic right ventricular cardiomyopathy: results from a 10-year registry. , 2011, European heart journal.
[15] M. Link,et al. Prophylactic Implantable Defibrillator in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia and No Prior Ventricular Fibrillation or Sustained Ventricular Tachycardia , 2010, Circulation.
[16] J. Deharo,et al. Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice. , 2010, Europace.
[17] J. Seward,et al. Infiltrative cardiovascular diseases: cardiomyopathies that look alike. , 2010, Journal of the American College of Cardiology.
[18] Wojciech Zareba,et al. Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Proposed Modification of the Task Force Criteria , 2010, Circulation.
[19] Wojciech Zareba,et al. Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Proposed Modification of the Task Force Criteria , 2010, European heart journal.
[20] P. Nallari,et al. Comparison of Uhl's anomaly, right ventricular outflow tract ventricular tachycardia (RVOT VT) & arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) with an insight into genetics of ARVD/C. , 2010, The Indian journal of medical research.
[21] G. Marcus,et al. Efficacy of antiarrhythmic drugs in arrhythmogenic right ventricular cardiomyopathy: a report from the North American ARVC Registry. , 2009, Journal of the American College of Cardiology.
[22] F. Marchlinski,et al. Epicardial Substrate and Outcome With Epicardial Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia , 2009, Circulation.
[23] Ju Chen,et al. Cell-cell connection to cardiac disease. , 2009, Trends in cardiovascular medicine.
[24] D. Corrado,et al. Arrhythmogenic right ventricular cardiomyopathy , 2009, The Lancet.
[25] L. Mestroni,et al. Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline. , 2009, Journal of cardiac failure.
[26] F. Crea,et al. High prevalence of myocarditis mimicking arrhythmogenic right ventricular cardiomyopathy differential diagnosis by electroanatomic mapping-guided endomyocardial biopsy. , 2009, Journal of the American College of Cardiology.
[27] C. Bergh,et al. Right ventricular cardiomyopathy: timing of heart transplantation in Uhl's anomaly and arrythmogenic right ventricular cardiomyopathy , 2009, European journal of heart failure.
[28] Dudley J Pennell,et al. Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity. , 2008, Journal of the American College of Cardiology.
[29] M. Silengo,et al. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy. , 2008, European journal of medical genetics.
[30] Harlan M Krumholz,et al. ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemaker , 2008, Journal of the American College of Cardiology.
[31] Harlan M Krumholz,et al. ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemaker , 2008, Circulation.
[32] Mark A Hlatky,et al. ACC/AHA/HRS 2008 guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: executive summary. , 2008, Heart rhythm.
[33] H. Calkins,et al. Mechanisms of Disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy , 2008, Nature Clinical Practice Cardiovascular Medicine.
[34] Sean Connors,et al. Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. , 2008, American journal of human genetics.
[35] J. Saffitz,et al. A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy. , 2007, American journal of human genetics.
[36] R. Baughman. Pulmonary hypertension associated with sarcoidosis , 2007, Arthritis research & therapy.
[37] Petros Syrris,et al. Clinical and Genetic Characterization of Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Provides Novel Insights Into Patterns of Disease Expression , 2007, Circulation.
[38] P. Syrris,et al. Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2. , 2006, American journal of human genetics.
[39] S. Russell,et al. Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2006, Journal of the American College of Cardiology.
[40] Dan M. Roden,et al. ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: A report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines , 2006 .
[41] L. Daliento,et al. Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia. , 2006, European journal of obstetrics, gynecology, and reproductive biology.
[42] Hugh Calkins,et al. DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2006, American journal of human genetics.
[43] D. Corrado,et al. Arrhythmogenic right ventricular cardiomyopathy/dysplasia: clinical impact of molecular genetic studies. , 2006, Circulation.
[44] Hyun Kim,et al. Linear Discrepancy of the Product of Two Chains , 2005, Order.
[45] M. Simpson,et al. Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy , 2005, Circulation.
[46] P. Syrris,et al. Genetics of Right Ventricular Cardiomyopathy , 2005, Journal of cardiovascular electrophysiology.
[47] S. Russell,et al. Arrhythmogenic Right Ventricular Dysplasia: A United States Experience , 2005, Circulation.
[48] J. Towbin,et al. Task Force 4: HCM and other cardiomyopathies, mitral valve prolapse, myocarditis, and Marfan syndrome. , 2005, Journal of the American College of Cardiology.
[49] Gian Antonio Danieli,et al. Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. , 2005, Cardiovascular Research.
[50] Hugh Calkins,et al. Noninvasive detection of myocardial fibrosis in arrhythmogenic right ventricular cardiomyopathy using delayed-enhancement magnetic resonance imaging. , 2005, Journal of the American College of Cardiology.
[51] G. Thiene,et al. Adipositas cordis, fatty infiltration of the right ventricle, and arrhythmogenic right ventricular cardiomyopathy. Just a matter of fat? , 2005, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.
[52] S. Sen-Chowdhry,et al. Arrhythmogenic right ventricular cardiomyopathy: clinical presentation, diagnosis, and management. , 2004, The American journal of medicine.
[53] Walter Birchmeier,et al. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy , 2004, Nature Genetics.
[54] N. Protonotarios,et al. Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy. , 2004, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.
[55] G. Schreiner,et al. B-Type Natriuretic Peptide Exerts Broad Functional Opposition to Transforming Growth Factor-&bgr; in Primary Human Cardiac Fibroblasts: Fibrosis, Myofibroblast Conversion, Proliferation, and Inflammation , 2004, Circulation research.
[56] M. Link,et al. Implantable Cardioverter-Defibrillator Therapy for Prevention of Sudden Death in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia , 2003, Circulation.
[57] D. Malicier,et al. Circumstances of Death and Gross and Microscopic Observations in a Series of 200 Cases of Sudden Death Associated With Arrhythmogenic Right Ventricular Cardiomyopathy and/or Dysplasia , 2003, Circulation.
[58] S. Rosenheck,et al. Arrhythmogenic Right Ventricular Dysplasia A Recessive Mutation in Desmoplakin Causes Arrhythmogenic Right Ventricular Dysplasia, Skin Disorder, and Woolly Hair , 2003 .
[59] L. Mestroni,et al. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. , 2003, Journal of the American College of Cardiology.
[60] M. Michalodimitrakis,et al. Left Side Right Ventricular Cardiomyopathy , 2002, Medicine, science, and the law.
[61] Z. Bulbul,et al. Successful surgical repair of Uhl's anomaly , 2002, Cardiology in the Young.
[62] C. Tondo,et al. Electrophysiological characteristics and outcome in patients with idiopathic right ventricular arrhythmia compared with arrhythmogenic right ventricular dysplasia , 2002, Heart.
[63] P. Thompson,et al. Arrhythmogenic right ventricular cardiomyopathy. , 2001, Journal of the American College of Cardiology.
[64] T. Kadono,et al. A case of Uhl anomaly treated with one and a half ventricle repair combined with partial right ventriculectomy in infancy. , 2001, The Journal of thoracic and cardiovascular surgery.
[65] C. D. De Pasquale,et al. Left sided arrhythmogenic ventricular dysplasia in siblings , 2001, Heart.
[66] D. Corrado,et al. Dispersion of Ventricular Depolarization-Repolarization: A Noninvasive Marker for Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy , 2001, Circulation.
[67] G. Thiene,et al. Arrhythmogenic right ventricular cardiomyopathy: An update. , 2001, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.
[68] D. Stephan,et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). , 2001, Human molecular genetics.
[69] S. Priori,et al. Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia , 2001, Circulation.
[70] D. Kelsell,et al. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. , 2000, Human molecular genetics.
[71] M. Duran,et al. Miocardiopatía dilatada en las displasias del ectodermo. Observaciones electroecocardiográficas en la hiperqueratosis palmoplantar con pelo lanoso , 2000 .
[72] A. Crosby,et al. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease) , 2000, The Lancet.
[73] D. Corrado,et al. CARDIOMYOPATHY Arrhythmogenic right ventricular cardiomyopathy: diagnosis, prognosis, and treatment , 2022 .
[74] J. Seidman,et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. , 1999, The New England journal of medicine.
[75] D. Corrado,et al. Cardiovascular causes of sudden death in young individuals including athletes. , 1999, Cardiology in review.
[76] D. Heudes,et al. Diagnosis of drowning by combined computer-assisted histomorphometry of lungs with blood strontium determination. , 1998, Journal of forensic sciences.
[77] S. Ratel,et al. Pathology of arrhythmogenic right ventricular cardiomyopathy/dysplasia--an autopsy study of 20 forensic cases. , 1998, Journal of forensic sciences.
[78] C. Furlanello,et al. Cardiac Arrest and Sudden Death in Competitive Athletes with Arrhythmogenic Right Ventricular Dysplasia , 1998, Pacing and clinical electrophysiology : PACE.
[79] J. Thomas,et al. Comparison of mortality rates and progression of left ventricular dysfunction in patients with idiopathic dilated cardiomyopathy and dilated versus nondilated right ventricular cavities. , 1997, The American journal of cardiology.
[80] M. Davies,et al. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. , 1997, Journal of the American College of Cardiology.
[81] M. Feucht,et al. VEGF induces cardiovascular malformation and embryonic lethality. , 1997, The American journal of pathology.
[82] C Berzuini,et al. Value of right ventricular ejection fraction in predicting short-term prognosis of patients with severe chronic heart failure. , 1997, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.
[83] N. Danchin,et al. Additional predictive value of both left and right ventricular ejection fractions on long-term survival in idiopathic dilated cardiomyopathy. , 1997, European heart journal.
[84] M. Enriquez-Sarano,et al. Determinants of pulmonary hypertension in left ventricular dysfunction. , 1997, Journal of the American College of Cardiology.
[85] A. Angelini,et al. Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis? , 1996, Circulation.
[86] P. Coumel,et al. Determinants of spontaneous occurrence of sustained monomorphic ventricular tachycardia in right ventricular dysplasia. , 1996, Journal of the American College of Cardiology.
[87] T. N. James,et al. Complete heart block and fatal right ventricular failure in an infant. , 1996, Circulation.
[88] H. Uhl. Uhl's anomaly revisited. , 1996, Circulation.
[89] G. J. Davis,et al. Extensive fibrofatty infiltration of the left ventricle in two cases of sudden cardiac death. , 1994, Journal of forensic sciences.
[90] P. Poole‐Wilson,et al. Reduced content of connexin43 gap junctions in ventricular myocardium from hypertrophied and ischemic human hearts. , 1993, Circulation.
[91] S. Ho,et al. Dysplastic conditions of the right ventricular myocardium: Uhl's anomaly vs arrhythmogenic right ventricular dysplasia. , 1993, British heart journal.
[92] M. Sporn,et al. Transforming growth factor-beta: recent progress and new challenges , 1992, The Journal of cell biology.
[93] F. Pelliccia,et al. Pathologic evidence of extensive left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy. , 1992, Human pathology.
[94] G. Breithardt,et al. Efficacy of Antiarrhythmic Drugs in Patients With Arrhythmogenic Right Ventricular Disease: Results in Patients With Inducible and Noninducible Ventricular Tachycardia , 1992, Circulation.
[95] G. Sinagra,et al. Left ventricular involvement in right ventricular dysplasia. , 1992, American heart journal.
[96] C. Green,et al. Altered patterns of gap junction distribution in ischemic heart disease. An immunohistochemical study of human myocardium using laser scanning confocal microscopy. , 1991, The American journal of pathology.
[97] D. Corrado,et al. Right ventricular cardiomyopathy: is there evidence of an inflammatory aetiology? , 1991, European heart journal.
[98] D. Corrado,et al. Sudden death in young competitive athletes: clinicopathologic correlations in 22 cases. , 1990, The American journal of medicine.
[99] G. Wager,et al. Antenatal ultrasound findings in a case of Uhl's anomaly. , 1988, American journal of perinatology.
[100] D. Corrado,et al. Right ventricular cardiomyopathy and sudden death in young people. , 1988, The New England journal of medicine.
[101] B. McManus,et al. Idiopathic dilated cardiomyopathy: analysis of 152 necropsy patients. , 1987, The American journal of cardiology.
[102] A. Pavie,et al. Signification des troubles de conduction intraventriculaires observés dans la dysplasie ventriculaire droite arythmogène , 1984 .
[103] C. Cottrill,et al. Pulmonary atresia with intact ventricular septum and ventriculocoronary communications: surgical significance. , 1982, Circulation.
[104] R Frank,et al. Right Ventricular Dysplasia: A Report of 24 Adult Cases , 1982, Circulation.
[105] G. Hutchins,et al. Cardiac Sarcoid: A Clinicopathologic Study of 84 Unselected Patients with Systemic Sarcoidosis , 1978, Circulation.
[106] H. Uhl. A previously undescribed congenital malformation of the heart: almost total absence of the myocardium of the right ventricle. , 1952, Bulletin of the Johns Hopkins Hospital.