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Genetic testing for familial hypertrophic cardiomyopathy in newborn infants.
Ryan MP, French J, al-Mahdawi S, Nihoyannopoulos P, Cleland JG, Oakley CM, Harper PS, Clarke A, Davis J, Grigg L. Ryan MP, et al. Among authors: nihoyannopoulos p. BMJ. 1995 Apr 1;310(6983):856-9. doi: 10.1136/bmj.310.6983.856. BMJ. 1995. PMID: 7677835 Free PMC article. No abstract available.
The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy.
Ryan MP, Cleland JG, French JA, Joshi J, Choudhury L, Chojnowska L, Michalak E, al-Mahdawi S, Nihoyannopoulos P, Oakley CM. Ryan MP, et al. Among authors: nihoyannopoulos p. Am J Cardiol. 1995 Oct 1;76(10):689-94. doi: 10.1016/s0002-9149(99)80198-2. Am J Cardiol. 1995. PMID: 7572626 Clinical Trial.
QT-interval abnormalities in hypertrophic cardiomyopathy.
Dritsas A, Sbarouni E, Gilligan D, Nihoyannopoulos P, Oakley CM. Dritsas A, et al. Among authors: nihoyannopoulos p. Clin Cardiol. 1992 Oct;15(10):739-42. doi: 10.1002/clc.4960151010. Clin Cardiol. 1992. PMID: 1395184 Free article.
The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene.
al-Mahdawi S, Chamberlain S, Chojnowska L, Michalak E, Nihoyannopoulos P, Ryan M, Kusnierczyk B, French JA, Gilligan DM, Cleland J, et al. al-Mahdawi S, et al. Among authors: nihoyannopoulos p. Br Heart J. 1994 Aug;72(2):105-11. doi: 10.1136/hrt.72.2.105. Br Heart J. 1994. PMID: 7848420 Free PMC article.
403 results