1H- and 31P-myocardial magnetic resonance spectroscopy in non-obstructive hypertrophic cardiomyopathy patients and competitive athletes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology, Nuclear Medicine and imaging,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11547-016-0718-2.pdf
Reference41 articles.
1. Charron P, Carrier L, Dubourg O et al (1997) Penetrance of familial hypertrophic cardiomyopathy. Genet Couns 8:107–114
2. Maron BJ, Gardin JM, Flack JM et al (1995) 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 92:785–789
3. Crilley JG, Boehm EA, Blair E et al (2003) Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy. J Am Coll Cardiol 41:1776–1782
4. Van Driest SL, Ommen SR, Tajik AJ et al (2005) Sarcomeric genotyping in hypertrophic cardiomyopathy. Mayo Clin Proc 80:463–469. doi: 10.1016/S0025-6196(11)63196-0
5. Wigle ED (2001) Cardiomyopathy: the diagnosis of hypertrophic cardiomyopathy. Heart 86:709–714
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