"Primary" dilated hearts.
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[1] Marco Merlo,et al. Insights into mildly dilated cardiomyopathy: temporal evolution and long‐term prognosis , 2017, European journal of heart failure.
[2] James A. White,et al. Late Gadolinium Enhancement and the Risk for Ventricular Arrhythmias or Sudden Death in Dilated Cardiomyopathy: Systematic Review and Meta-Analysis. , 2017, JACC. Heart failure.
[3] S. Cook,et al. Truncating Variants in Filamin C: The Challenges of Genotype-Phenotype Correlations in Cardiomyopathies. , 2016, Journal of the American College of Cardiology.
[4] L. Calò,et al. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. , 2016, Journal of the American College of Cardiology.
[5] C. Yancy,et al. Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association. , 2016, Circulation.
[6] J. Kluger,et al. Late Gadolinium Enhancement in Patients with Nonischemic Dilated Cardiomyopathy , 2016, Pacing and clinical electrophysiology : PACE.
[7] Sabino Iliceto,et al. Nonischemic Left Ventricular Scar as a Substrate of Life-Threatening Ventricular Arrhythmias and Sudden Cardiac Death in Competitive Athletes , 2016, Circulation. Arrhythmia and electrophysiology.
[8] S. Heymans,et al. Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases. , 2016, European heart journal.
[9] S. Iliceto,et al. Clinical presentation and diagnosis of myocarditis , 2015, Heart.
[10] A. Kadish,et al. Sudden cardiac death risk stratification in patients with nonischemic dilated cardiomyopathy. , 2014, Journal of the American College of Cardiology.
[11] C. Kramer,et al. Late Gadolinium Enhancement on Cardiac Magnetic Resonance Predicts Adverse Cardiovascular Outcomes in Nonischemic Cardiomyopathy: A Systematic Review and Meta-Analysis , 2014, Circulation. Cardiovascular imaging.
[12] P. Elliott. Classification of cardiomyopathies: evolution or revolution? , 2013, Journal of the American College of Cardiology.
[13] Tiina Heliö,et al. 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. , 2013, European heart journal.
[14] G. Bonne,et al. ‘State-of-the-heart’ of cardiac laminopathies , 2013, Current opinion in cardiology.
[15] E. Rampersaud,et al. Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy. , 2013, Journal of cardiac failure.
[16] E. McNally,et al. Genetic mutations and mechanisms in dilated cardiomyopathy. , 2013, The Journal of clinical investigation.
[17] A. Angelini,et al. Classification and histological, immunohistochemical, and molecular diagnosis of inflammatory myocardial disease , 2013, Heart Failure Reviews.
[18] D. Corrado,et al. Pathophysiology of arrhythmogenic cardiomyopathy , 2012, Nature Reviews Cardiology.
[19] A. Zwinderman,et al. Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study. , 2012, Journal of the American College of Cardiology.
[20] L. A. Bonet,et al. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012 , 2010, European journal of heart failure.
[21] A. Mansur,et al. Mutations in the human phospholamban gene in patients with heart failure. , 2011, American heart journal.
[22] R. Hershberger,et al. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. , 2011, Journal of the American College of Cardiology.
[23] Ana Morales,et al. Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2009, Circulation. Heart failure.
[24] Matthias Gutberlet,et al. Cardiovascular Magnetic Resonance in Myocarditis: A JACC White Paper , 2009 .
[25] P. Rahko,et al. Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. , 2008, American heart journal.
[26] Eloisa Arbustini,et al. Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. , 2007, European heart journal.
[27] I. V. Van Gelder,et al. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. , 2007, American heart journal.
[28] M. Michels,et al. Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience , 2007, Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.
[29] B. Soliven,et al. Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy. , 2006, Journal of the American College of Cardiology.
[30] Barry J Maron,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 Interd , 2006, Circulation.
[31] M. Simpson,et al. Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy , 2005, Circulation.
[32] R. Hershberger,et al. Clinical and genetic issues in familial dilated cardiomyopathy. , 2005, Journal of the American College of Cardiology.
[33] E. Kranias,et al. Calcium: Phospholamban: a crucial regulator of cardiac contractility , 2003, Nature Reviews Molecular Cell Biology.
[34] Ulrike Mende,et al. Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban , 2003, Science.
[35] Y. Doi,et al. Long-term prognosis of patients with mildly dilated cardiomyopathy. , 2002, Circulation journal : official journal of the Japanese Circulation Society.
[36] S. Bione,et al. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. , 2000, American journal of human genetics.
[37] L. Mestroni,et al. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. , 2000, Circulation.
[38] 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.
[39] F. Muntoni,et al. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy , 1999, Nature Genetics.
[40] H. Katus,et al. Frequency and phenotypes of familial dilated cardiomyopathy. , 1998, Journal of the American College of Cardiology.
[41] B Maisch,et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. , 1996, Circulation.
[42] A. Gavazzi,et al. The spectrum of left ventricular size in dilated cardiomyopathy: clinical correlates and prognostic implications. SPIC (Italian Multicenter Cardiomyopathy Study) Group. , 1993, American heart journal.
[43] W. Abelmann,et al. Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop. , 1992, The American journal of cardiology.
[44] A. Tajik,et al. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. , 1992, The New England journal of medicine.
[45] R L Popp,et al. Mildly dilated congestive cardiomyopathy. Use of prospective diagnostic criteria and description of the clinical course without heart transplantation. , 1990, Circulation.
[46] Y. Sugishita,et al. Clinical characteristics of cardiomyopathy with mild dilatation. , 1990, Journal of cardiology.
[47] L. Melton,et al. Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984. , 1989, Circulation.
[48] R L Popp,et al. Mildly dilated congestive cardiomyopathy. , 1985, Circulation.