메뉴 건너뛰기




Volumn 12, Issue 6, 2006, Pages 422-429

Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy

Author keywords

Dilated cardiomyopathy; Family studies; Genetics

Indexed keywords

AGE DISTRIBUTION; ARTICLE; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DISEASE COURSE; ETHNICITY; EVALUATION; FAMILIAL DILATED CARDIOMYOPATHY; FAMILY; FAMILY HISTORY; HEART LEFT VENTRICLE PERFORMANCE; HEART TRANSPLANTATION; HUMAN; INHERITANCE; PRIORITY JOURNAL; ADOLESCENT; ADULT; AGED; CARDIOVASCULAR SYSTEM; CHILD; DEATH; FEMALE; GENETICS; INFANT; MALE; MEDICAL RECORD; MIDDLE AGED; PATHOPHYSIOLOGY; PEDIGREE; PRESCHOOL CHILD; TIME;

EID: 33750143766     PISSN: 10719164     EISSN: 15328414     Source Type: Journal    
DOI: 10.1016/j.cardfail.2006.03.009     Document Type: Article
Times cited : (38)

References (30)
  • 2
    • 14644427123 scopus 로고    scopus 로고
    • Genetic causes of human heart failure
    • Morita H., Seidman J., and Seidman C.E. Genetic causes of human heart failure. J Clin Invest 115 (2005) 518-526
    • (2005) J Clin Invest , vol.115 , pp. 518-526
    • Morita, H.1    Seidman, J.2    Seidman, C.E.3
  • 3
    • 15944403997 scopus 로고    scopus 로고
    • Clinical and genetic issues in familial dilated cardiomyopathy
    • Burkett E.L., and Hershberger R.E. Clinical and genetic issues in familial dilated cardiomyopathy. J Am Coll Cardiol 45 (2005) 969-981
    • (2005) J Am Coll Cardiol , vol.45 , pp. 969-981
    • Burkett, E.L.1    Hershberger, R.E.2
  • 5
    • 0019468424 scopus 로고
    • Follow-up study in congestive (dilated) cardiomyopathy
    • Lengyel M., and Kökeny M. Follow-up study in congestive (dilated) cardiomyopathy. Acta Cardiol 36 (1981) 35-48
    • (1981) Acta Cardiol , vol.36 , pp. 35-48
    • Lengyel, M.1    Kökeny, M.2
  • 6
    • 0021875572 scopus 로고
    • Familial aggregation of idiopathic dilated cardiomyopathy
    • Michels V.V., Driscoll D.J., and Miller F.A. Familial aggregation of idiopathic dilated cardiomyopathy. Am J Cardiol 55 (1985) 1232-1233
    • (1985) Am J Cardiol , vol.55 , pp. 1232-1233
    • Michels, V.V.1    Driscoll, D.J.2    Miller, F.A.3
  • 7
    • 0022588513 scopus 로고
    • Congestive cardiomyopathy in infants and children
    • Pongpanich B., and Isaraprasart S. Congestive cardiomyopathy in infants and children. Jap Heart J 27 (1986) 11-15
    • (1986) Jap Heart J , vol.27 , pp. 11-15
    • Pongpanich, B.1    Isaraprasart, S.2
  • 9
    • 0024508590 scopus 로고
    • Frequency of familial nature of dilated cardiomyopathy and usefulness of cardiac transplantation in this subset
    • Valantine H.A., Hunt S.A., Fowler M.B., Billingham M.E., and Schroeder J.S. Frequency of familial nature of dilated cardiomyopathy and usefulness of cardiac transplantation in this subset. Am J Cardiol 63 (1989) 959-963
    • (1989) Am J Cardiol , vol.63 , pp. 959-963
    • Valantine, H.A.1    Hunt, S.A.2    Fowler, M.B.3    Billingham, M.E.4    Schroeder, J.S.5
  • 11
    • 0027452813 scopus 로고
    • Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families
    • Zachara E., Caforio A.L.P., Carboni G.P., Pellegrini A., Pompili A., Del Porto G., et al. Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families. Br Heart J 69 (1993) 129-135
    • (1993) Br Heart J , vol.69 , pp. 129-135
    • Zachara, E.1    Caforio, A.L.P.2    Carboni, G.P.3    Pellegrini, A.4    Pompili, A.5    Del Porto, G.6
  • 12
    • 0029026134 scopus 로고
    • Familial aggregation of dilated cardiomyopathy. Evaluation of clinical characteristics and prognosis
    • Honda Y., Yokota Y., and Yokoyama M. Familial aggregation of dilated cardiomyopathy. Evaluation of clinical characteristics and prognosis. Japan Circ J 59 (1995) 589-598
    • (1995) Japan Circ J , vol.59 , pp. 589-598
    • Honda, Y.1    Yokota, Y.2    Yokoyama, M.3
  • 14
    • 0026319459 scopus 로고
    • The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
    • Michels V.V., Moll P.P., Miller F.A., Tajik A.J., Chu J.S., Driscoll D.J., et al. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med 326 (1992) 77-82
    • (1992) N Engl J Med , vol.326 , pp. 77-82
    • Michels, V.V.1    Moll, P.P.2    Miller, F.A.3    Tajik, A.J.4    Chu, J.S.5    Driscoll, D.J.6
  • 17
    • 0030871639 scopus 로고    scopus 로고
    • Idiopathic dilated cardiomyopathy: familial prevalence and HLA distribution
    • McKenna C., Codd M., McCann H., and Sugrue D. Idiopathic dilated cardiomyopathy: familial prevalence and HLA distribution. Heart 77 (1997) 549-552
    • (1997) Heart , vol.77 , pp. 549-552
    • McKenna, C.1    Codd, M.2    McCann, H.3    Sugrue, D.4
  • 19
    • 0031885093 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease
    • Baig M.K., Goldman J.H., Caforio A.P., Coonar A.S., Keeling P.J., and McKenna W.J. 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.P.3    Coonar, A.S.4    Keeling, P.J.5    McKenna, W.J.6
  • 20
    • 0033165780 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group
    • Mestroni L., Rocco C., Gregori D., Sinagra G., Di Lenarda A., Miocic S., et al. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. J Am Coll Cardiol 34 (1999) 181-190
    • (1999) J Am Coll Cardiol , vol.34 , pp. 181-190
    • Mestroni, L.1    Rocco, C.2    Gregori, D.3    Sinagra, G.4    Di Lenarda, A.5    Miocic, S.6
  • 22
    • 0038037680 scopus 로고    scopus 로고
    • Progression of familial and non-familial dilated cardiomyopathy: long term follow up
    • Michels V.V., Driscoll D.J., Miller F.A., Olson T.M., Atkinson E.J., Olswold C.L., et al. Progression of familial and non-familial dilated cardiomyopathy: long term follow up. Heart 89 (2003) 757-761
    • (2003) Heart , vol.89 , pp. 757-761
    • Michels, V.V.1    Driscoll, D.J.2    Miller, F.A.3    Olson, T.M.4    Atkinson, E.J.5    Olswold, C.L.6
  • 23
    • 0032852339 scopus 로고    scopus 로고
    • Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice
    • Crispell K., Wray A., Ni H., Nauman D., and Hershberger R. Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice. J Am Coll Cardiol 34 (1999) 837-847
    • (1999) J Am Coll Cardiol , vol.34 , pp. 837-847
    • Crispell, K.1    Wray, A.2    Ni, H.3    Nauman, D.4    Hershberger, R.5
  • 24
    • 0034820958 scopus 로고    scopus 로고
    • Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
    • Jakobs P.M., Hanson E., Crispell K.A., Toy W., Keegan H., Schilling K., et al. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease. J Card Fail 7 (2001) 249-256
    • (2001) J Card Fail , vol.7 , pp. 249-256
    • Jakobs, P.M.1    Hanson, E.2    Crispell, K.A.3    Toy, W.4    Keegan, H.5    Schilling, K.6
  • 25
    • 0036911038 scopus 로고    scopus 로고
    • A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation
    • Hershberger R.E., Hanson E., Jakobs P.M., Keegan H., Coates K., Bousman S., et al. A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation. Am Heart J 144 (2002) 1081-1086
    • (2002) Am Heart J , vol.144 , pp. 1081-1086
    • Hershberger, R.E.1    Hanson, E.2    Jakobs, P.M.3    Keegan, H.4    Coates, K.5    Bousman, S.6
  • 26
    • 0036174030 scopus 로고    scopus 로고
    • Cardiac troponin T lysine-210 deletion in a family with dilated cardiomyopathy
    • Hanson E., Jakobs P., Keegan H., Coates K., Bousman S., Dienel N., et al. Cardiac troponin T lysine-210 deletion in a family with dilated cardiomyopathy. J Card Fail 8 (2002) 28-32
    • (2002) J Card Fail , vol.8 , pp. 28-32
    • Hanson, E.1    Jakobs, P.2    Keegan, H.3    Coates, K.4    Bousman, S.5    Dienel, N.6
  • 27
    • 0030768395 scopus 로고    scopus 로고
    • Distribution and categorization of echocardiographic measurements in relation to reference limits. The Framingham Heart Study: formulation of a height- and sex-specific classification and its prospective validation
    • Vasan R., Larson M., Levy D., Evans J., and Benjamin E. Distribution and categorization of echocardiographic measurements in relation to reference limits. The Framingham Heart Study: formulation of a height- and sex-specific classification and its prospective validation. Circulation 96 (1997) 1863-1873
    • (1997) Circulation , vol.96 , pp. 1863-1873
    • Vasan, R.1    Larson, M.2    Levy, D.3    Evans, J.4    Benjamin, E.5
  • 28
    • 0032883646 scopus 로고    scopus 로고
    • Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected
    • Hershberger R.E., Ni H., and Crispell K.A. Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected. J Cardiac Failure 51 (1999) 203-212
    • (1999) J Cardiac Failure , vol.51 , pp. 203-212
    • Hershberger, R.E.1    Ni, H.2    Crispell, K.A.3
  • 30


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.