Results 151 to 160 of about 44,322 (189)
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Heart, Lung and Circulation, 2020
Amyloid cardiomyopathy is emerging as an important and under-recognised cause of heart failure and cardiac arrhythmias, especially in older adults. This disorder is characterised by extracellular deposition of amyloid fibrils that form due to misfolding of secreted light chains (AL) or transthyretin protein (ATTR). In ATTR, amyloid aggregates typically
Nicole K. Bart +5 more
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Amyloid cardiomyopathy is emerging as an important and under-recognised cause of heart failure and cardiac arrhythmias, especially in older adults. This disorder is characterised by extracellular deposition of amyloid fibrils that form due to misfolding of secreted light chains (AL) or transthyretin protein (ATTR). In ATTR, amyloid aggregates typically
Nicole K. Bart +5 more
openaire +5 more sources
JAMA, 1999
The degree of clinical expression of both obstructive and nonobstructive hypertrophic cardiomyopathy (HCM) is widely variable. Many patients with HCM are asymptomatic or minimally symptomatic. Most patients with mild or moderate HCM respond well to medical therapy, but medical therapy in patients with severe disease is only marginally beneficial.
Maron, B J +8 more
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The degree of clinical expression of both obstructive and nonobstructive hypertrophic cardiomyopathy (HCM) is widely variable. Many patients with HCM are asymptomatic or minimally symptomatic. Most patients with mild or moderate HCM respond well to medical therapy, but medical therapy in patients with severe disease is only marginally beneficial.
Maron, B J +8 more
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American Journal of Roentgenology, 2008
The aims of this article are to present the main features of MRI of cardiomyopathy and to show selected images of cardiomyopathies.Cardiomyopathy is a frequent reason for cardiac MRI evaluation, which is now considered the most appropriate imaging technique for the diagnosis and follow-up of this wide range of myocardial diseases.
Belloni, E +6 more
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The aims of this article are to present the main features of MRI of cardiomyopathy and to show selected images of cardiomyopathies.Cardiomyopathy is a frequent reason for cardiac MRI evaluation, which is now considered the most appropriate imaging technique for the diagnosis and follow-up of this wide range of myocardial diseases.
Belloni, E +6 more
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Modern Imaging Techniques in Cardiomyopathies
Circulation Research, 2017 Modern advanced imaging techniques have allowed increasingly more rigorous assessment of the cardiac structure and function of several types of cardiomyopathies. In contemporary cardiology practice, echocardiography and cardiac magnetic resonance imaging
M Fuad Jan
exaly +2 more sources
Nursing Standard, 2004
Cardiomyopathy is a disease of the heart muscle. There are four main types of cardiomyopathy and each can affect people differently. This article discusses the signs and symptoms, diagnosis and treatment for the different types of the disease, the importance of genetic screening and risk stratification, and the nurse'a role in patient management.
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Cardiomyopathy is a disease of the heart muscle. There are four main types of cardiomyopathy and each can affect people differently. This article discusses the signs and symptoms, diagnosis and treatment for the different types of the disease, the importance of genetic screening and risk stratification, and the nurse'a role in patient management.
openaire +2 more sources
Current Problems in Cardiology, 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.
Steve R, Ommen, Rick A, Nishimura
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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.
Steve R, Ommen, Rick A, Nishimura
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Phaeochromocytoma and cardiomyopathy
Medical Journal of Australia, 1988This case report describes a patient who presented with severe biventricular cardiac failure and shock, whose cardiac function returned to normal after the removal of a noradrenaline-secreting benign phaeochromocytoma. A catecholamine-induced cardiomyopathy with cardiogenic shock, rather than catecholamine-mediated peripheral vasoconstriction alone, is
SCOTT,, PARKES, R, CAMERON, DP
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Cardiology in the Young, 1977
AbstractHypertrophic cardiomyopathy is a common, inherited heart disease with a heterogeneous clinical presentation and natural history. Recently, advances in diagnosis and treatment options have been instrumental in decreasing the frequency of adverse clinical events; however, complete elimination of sudden cardiac death still remains an elusive gain.
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AbstractHypertrophic cardiomyopathy is a common, inherited heart disease with a heterogeneous clinical presentation and natural history. Recently, advances in diagnosis and treatment options have been instrumental in decreasing the frequency of adverse clinical events; however, complete elimination of sudden cardiac death still remains an elusive gain.
openaire +4 more sources