1949
DOI: 10.1136/hrt.11.1.68
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Familial Cardiomegaly

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Cited by 181 publications
(30 citation statements)
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“…The clinical picture corresponds to that of familial cardiomyopathy, described by Evans [2] in 1949, and well reviewed in recent years [1,2,8,9].…”
Section: Discussionmentioning
confidence: 99%
“…The clinical picture corresponds to that of familial cardiomyopathy, described by Evans [2] in 1949, and well reviewed in recent years [1,2,8,9].…”
Section: Discussionmentioning
confidence: 99%
“…Although familial occurrence was described in 1949, 28 it was subsequently shown that inheritance was through an autosomal dominant mechanism. 32,41 In 1990, C. Seidman and J.G.…”
Section: Genetic Eramentioning
confidence: 99%
“…27 In 1949, Evans reported that idiopathic ventricular hypertrophy may, in some instances, be familial. 28 In 1958, Donald Teare-a pathologist-studied the hearts of 9 patients with left ventricular hypertrophy, 8 of whom had died suddenly; he reported that the hypertrophy was asymmetrical and most severe in the ventricular septum 29 ( Figure 4 in the article by McKenna et al 11 ). Thus, by 1958, the condition now termed HCM had the following characteristics: asymmetrical left ventricular hypertrophy causing obstruction to ventricular outflow, a familial association in some patients and an increased risk of arrhythmias, and sudden cardiac death.…”
Section: Hypertrophic Cardiomyopathy Early Yearsmentioning
confidence: 99%
“…В 1949 г. Evans W. обнаружил в 2 семьях 5 пациен-тов с выраженной гипертрофией миокарда ЛЖ, что назвал «семейной кардиомегалией» [17].…”
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