Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience-Reference-Cited by-同舟云学术

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Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience

Published:2007-05 Issue:5 Volume:15 Page:184-190
ISSN:1568-5888
Container-title:Netherlands Heart Journal
language:nl
Short-container-title:NHJL

Author:

Michels M.,Hoedemaekers Y. M.,Kofflard M. J.,Frohn-Mulder I.,Dooijes D.,Majoor-Krakauer D.,Cate F. J. Ten

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03085978.pdf

Reference42 articles.

1. Zou Y, Song L, Wang Z, Ma A, Liu T, Gu H, et al. Prevalence of idiopathic hypertrophic cardiomyopathy in China: a populationbased echocardiographic analysis of 8080 adults. Am J Med 2004; 116:14-8.

2. Maron BJ, Gardin JM, Flack JM, Gidding SS, Kurosaki TT, Bild DE. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation 1995;92:785-9.

3. Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003;107:2227-32.

4. Van Driest SL, Ellsworth EG, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. Circulation 2003;108:445-51.

5. Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, Mc-Kenna W, Seidman CE, et al. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 1990;62:999-1006.

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2. Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy;Journal of the American College of Cardiology;2019-04

3. Prognostic significance of anterior mitral valve leaflet length in individuals with a hypertrophic cardiomyopathy gene mutation without hypertrophic changes;Journal of Ultrasound;2018-06-06

4. “Primary” dilated hearts;International Journal of Cardiology;2018-04

5. Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder Mutation;Circulation: Cardiovascular Genetics;2017-08

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