Design and implementation of the North American Pediatric Cardiomyopathy Registry.
暂无分享,去创建一个
E J Orav | S. Colan | S. Osganian | J. Towbin | L. Sleeper | E. Orav | S. Lipshultz | P. Lurie | J A Towbin | L A Sleeper | S E Lipshultz | S D Colan | G F Cox | M A Grenier | S K Osganian | P R Lurie | G. Cox | M. Grenier
[1] R. Gillum. Idiopathic cardiomyopathy in the United States, 1970-1982. , 1986, American heart journal.
[2] S. Nouri,et al. Clinical profile of conjestive cardiomyopathy in children , 1990 .
[3] S. Lipshultz,et al. Clinical approach to genetic cardiomyopathy in children. , 1996, Circulation.
[4] L. Melton,et al. Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984. , 1989, Circulation.
[5] S. Berger,et al. Sudden cardiac death in infants, children, and adolescents. , 1999, Pediatric clinics of North America.
[6] J. Steiner,et al. Chart reviews in emergency medicine research: Where are the methods? , 1996, Annals of emergency medicine.
[7] O. Ruuskanen,et al. Idiopathic Dilated Cardiomyopathy in Children: Prognostic Indicators and Outcome , 1998, Pediatrics.
[8] T. Spray,et al. Dilated cardiomyopathy in infants and children. , 1988, Journal of the American College of Cardiology.
[9] R. Doughty,et al. Epidemiology of heart failure and ventricular dysfunction , 1998, The Lancet.
[10] A. Keogh,et al. Timing of cardiac transplantation in idiopathic dilated cardiomyopathy. , 1988, The American journal of cardiology.
[11] A. Nadas,et al. The clinical course of primary myocardial disease in infants and children. , 1976, American heart journal.
[12] W. Stevenson,et al. Poor survival of patients with idiopathic cardiomyopathy considered too well for transplantation. , 1987, The American journal of medicine.
[13] A. Lewis,et al. Outcome of infants and children with dilated cardiomyopathy. , 1991, The American journal of cardiology.
[14] L N J Archer,et al. Heart Disease in Infants, Children and Adolescents including the Fetus and Young Adult , 1996 .
[15] S. Colan,et al. Developmental modulation of myocardial mechanics: age- and growth-related alterations in afterload and contractility. , 1992, Journal of the American College of Cardiology.
[16] B. McCrindle,et al. Long-term outcome and prognostic determinants in children with hypertrophic cardiomyopathy. , 1998, Journal of the American College of Cardiology.
[17] S. Lipshultz,et al. Pediatric Dilated Cardiomyopathy (DCM): Prognosis in a developing nation is comparable to developed nations , 1996 .
[18] R. Friedman,et al. Clinical course of idiopathic dilated cardiomyopathy in children. , 1991, Journal of the American College of Cardiology.
[19] H. Krumholz. Time to focus on the more typical heart-failure patients , 1998, The Lancet.
[20] J. Matthews,et al. Prognostic features of children with idiopathic dilated cardiomyopathy. , 1991, The American journal of cardiology.
[21] Arthur J. Moss,et al. Moss and Adams' heart disease in infants, children, and adolescents : including the fetus and young adult , 2016 .
[22] R. Rowe,et al. Natural history and prognostic risk factors in endocardial fibroelastosis. , 1988, The American journal of cardiology.
[23] O. Simell,et al. Epidemiology of idiopathic cardiomyopathies in children and adolescents. A nationwide study in Finland. , 1997, American journal of epidemiology.
[24] L. Benson,et al. Natural history of dilated cardiomyopathy in children. , 1991, American heart journal.
[25] J. Cordero. Registries of birth defects and genetic diseases. , 1992, Pediatric clinics of North America.
[26] J. Seward,et al. Idiopathic dilated cardiomyopathy in the young: clinical profile and natural history. , 1985, Journal of the American College of Cardiology.
[27] D. Fyler,et al. Nadas' Pediatric Cardiology , 1992 .