Genetic screening of cardiomyopathics;Genetisches screening bei kardiomypathien

Zeitschrift fur Kardiologie

Volumn 89, Issue 7, 2000, Pages 638-640

  Thierfelder, Ludwig ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

Cardiomyopathics; Genetics

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CARDIOMYOPATHY; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HEART DILATATION; HEART VENTRICLE ARRHYTHMIA; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; PHENOTYPE; SUDDEN DEATH; COMPARATIVE STUDY; CONGESTIVE CARDIOMYOPATHY; DIFFERENTIAL DIAGNOSIS; GENETICS; HEART RIGHT VENTRICLE DYSPLASIA; MUTATION; RESTRICTIVE CARDIOMYOPATHY; RISK FACTOR;

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; CARDIOMYOPATHIES; CARDIOMYOPATHY, DILATED; CARDIOMYOPATHY, HYPERTROPHIC; CARDIOMYOPATHY, RESTRICTIVE; DEATH, SUDDEN, CARDIAC; DIAGNOSIS, DIFFERENTIAL; GENETIC SCREENING; GENOTYPE; HUMANS; MUTATION; PHENOTYPE; RISK FACTORS;

EID: 0033624241     PISSN: 03005860     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003920070215     Document Type: Article

References (11)

1. 1. Dec GW, Fuster V (1994) Idiopathic dilated cardiomyopathy [see comments]. N Engl J Med 331:1564-1575
2. 2. Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Muehle G, Johnson W, McDonough B (1999) Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med Dec 2, 341 (23):1715-1724
3. 3. Li D, Tapscoft T, Gonzalez O, Burch PE, Quinones MA, Zoghbi WA, Hill R, Bachinski LL, Mann DL, Roberts R (1999) Desmin mutation responsible for idiopathic dilated cardiomyopathy. Circulation Aug 3, 100(5):461-464
4. 4. Michels VV, Moll PP, Miller FA et al (1992) The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med 326:77-82
5. 5. Michels VV, Pastores GM, Moll PP et al (1993) Dystrophin analysis in idiopathic dilated cardiomyopathy. J Med Genet 30:955-957
6. 6. Olson TM, Michels VV, Thibodeau SN et al (1998) Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 280:750-752
7. 7. Richardson P, McKenna W, Bristow M et al (1996) Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 93:841-842
8. 8. Spirito P, Seidman CE, McKenna W, Maron BJ (1997) The management of hypertrophic cardiomyopathy. N Engl J Med Mar 13, 336(11):775-785
9. 9. Thierfelder L (1998) Genetics of dilated cardiomyopathy. Med Klin Apr 15, 93(4):210-214
10. 10. Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG et al (1995) Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med 332:1058-1064
11. 11. Wichter T, Borggrefe M. Breithardt G (1998) Arrhythmogenic right ventricular cardiomyopathy. Etiology, diagnosis and therapy. Med Klin Apr 15, 93(4):268-277