Results 211 to 220 of about 38,525 (259)
Genetic cardiomyopathy unmasked by pregnancy: X-linked dystrophinopathy presenting as peripartum cardiomyopathy-a case report. [PDF]
Eur Heart J Case RepBauer J +4 more
europepmc +1 more source
No Evidence for an Association Between DIP2B Repeat Expansion and Neurological Disease
Movement Disorders, EarlyView.
Chia‐Ying Ko +9 more
wiley +1 more source
Cardiomyopathies: An Overview [PDF]
International Journal of Molecular Sciences, 2021 Background: Cardiomyopathies are a heterogeneous group of pathologies characterized by structural and functional alterations of the heart. Aims: The purpose of this narrative review is to focus on the most important cardiomyopathies and their epidemiology, diagnosis, and management. Methods: Clinical trials were identified by Pubmed until 30 March 2021.
Mauro Giordano +2 more
exaly +4 more sources
Circulation Research, 2017 The nonischemic cardiomyopathies are a diverse group of cardiac disorders that frequently cause heart failure and death and are now recognized with increasing frequency. There has been substantial progress in the clinical recognition and understanding of the natural history of these conditions. Well-established and new techniques of cardiac imaging are
Eugene Braunwald
exaly +3 more sources
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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
openaire +5 more sources
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
openaire +5 more sources
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
openaire +5 more sources
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
openaire +2 more sources
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
openaire +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.
openaire +2 more sources
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
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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