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Still at sea: a patient's ongoing journey with non-obstructive hypertrophic cardiomyopathy. [PDF]
Eur Heart J Case RepGoldie FC, Myles RC, Coats CJ.
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Association between uric acid-to-albumin ratio and clinical outcomes in patients with hypertrophic cardiomyopathy: A retrospective observational study. [PDF]
J Int Med ResÜlgen Kunak A, Kunak T.
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Adult case of 17β-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency due to the p. Arg130Cys mutation of the <i>HSD17B10</i> gene: case report. [PDF]
AME Case RepKhodawrdi A +3 more
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CHAtRF Modulates Cardiac Hypertrophy via SRSF5-Dependent Regulation of Psmg4 Alternative Splicing. [PDF]
Research (Wash D C)Zhou LY +12 more
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Lancet, The, 2013
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant, cardiovascular disorder that carries the risk of sudden cardiac death. The prevalence of HCM is 1:500 persons. The purpose of this article is to provide an overview of the pathophysiology, symptoms, complications, diagnostic testing, and treatment.
Angelos G, Rigopoulos, Hubert, Seggewiss
exaly +11 more sources
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant, cardiovascular disorder that carries the risk of sudden cardiac death. The prevalence of HCM is 1:500 persons. The purpose of this article is to provide an overview of the pathophysiology, symptoms, complications, diagnostic testing, and treatment.
Angelos G, Rigopoulos, Hubert, Seggewiss
exaly +11 more sources
Lancet, The, 2004
Abstract The clinical definition of hypertrophic cardiomyopathy is left ventricular hypertrophy in the absence of other causes of left ventricular hypertrophy. The size and volume of the left ventricle are usually normal or smaller. Most cases are familial disease with autosomal dominant inheritance.
Perry M Elliott
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Abstract The clinical definition of hypertrophic cardiomyopathy is left ventricular hypertrophy in the absence of other causes of left ventricular hypertrophy. The size and volume of the left ventricle are usually normal or smaller. Most cases are familial disease with autosomal dominant inheritance.
Perry M Elliott
exaly +6 more sources
Child's Nervous System, 2015
Hypertrophic pachymeningitis (HP) is a rare clinical entity characterized by diffuse or localized fibrous thickening of the dura mater. It is well known but rare especially in pediatric population disease of differing origins. The primary (idiopathic) form is diagnosed after excluding other possible etiologies.
Tomasz, Dziedzic +3 more
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Hypertrophic pachymeningitis (HP) is a rare clinical entity characterized by diffuse or localized fibrous thickening of the dura mater. It is well known but rare especially in pediatric population disease of differing origins. The primary (idiopathic) form is diagnosed after excluding other possible etiologies.
Tomasz, Dziedzic +3 more
openaire +2 more sources