Results 351 to 360 of about 413,499 (385)
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Hypertrophic cardiomyopathy: a systematic review.

Journal of the American Medical Association (JAMA), 2002
CONTEXT Throughout the past 40 years, a vast and sometimes contradictory literature has accumulated regarding hypertrophic cardiomyopathy (HCM), a genetic cardiac disease caused by a variety of mutations in genes encoding sarcomeric proteins and ...
B. Maron
semanticscholar   +1 more source

Cardiomyopathy

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

Hypertrophic cardiomyopathy

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.
openaire   +4 more sources

Classification of cardiomyopathies

2018
For over 50 years, the definition and classification of cardiomyopathies have remained anchored in the concept of ventricular dysfunction and myocardial structural remodelling due to unknown cause. The concept of idiopathic was first challenged in 2006, when the American Heart Association classification subordinated the phenotype to the aetiology ...
SINAGRA, GIANFRANCO   +6 more
openaire   +3 more sources

Hypertrophic cardiomyopathy

The Lancet, 1998
Hypertrophic cardiomyopathy is a common genetically transmitted disease, defined clinically by the presence of unexplained left ventricular hypertrophy. The disease has a varied clinical course and outcome; many patients have little or no discernible cardiovascular symptoms, whereas others have profound exercise limitation and recurrent arrhythmias ...
Perry, Elliott, William J, McKenna
openaire   +3 more sources

MRI of Cardiomyopathy

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   +3 more sources

Takotsubo Cardiomyopathy

Heart Failure Clinics, 2013
Takotsubo cardiomyopathy (TTC) is a unique acute syndrome characterized by transient left ventricular systolic dysfunction in the absence of significant coronary artery disease, occurring mostly in postmenopausal women after emotional and/or physical stress.
Gianluigi Savarese   +9 more
openaire   +6 more sources

Pathophysiology of sepsis-induced cardiomyopathy

Nature Reviews Cardiology, 2021
S. Hollenberg, M. Singer
semanticscholar   +1 more source

The diabetic cardiomyopathy

Acta Diabetologica, 2010
Diabetic cardiomyopathy has been defined as "a distinct entity characterized by the presence of abnormal myocardial performance or structure in the absence of epicardial coronary artery disease, hypertension, and significant valvular disease". The diagnosis stems from the detection of myocardial abnormalities and the exclusion of other contributory ...
TARQUINI, ROBERTO   +4 more
openaire   +4 more sources

Treatable cardiomyopathies

The Indian Journal of Pediatrics, 2000
Cardiomyopathy is defined as primary myocardial dysfunction which is not due to hypertensive, valvular, congenital, coronary or pulmonary vascular disease. This term usually denotes a dismal prognosis short of cardiac transplantation. However, several organic diseases of the heart can result in right or left ventricular dysfunction resulting in ...
S. S. Prabhu, B. V. Dalvi
openaire   +4 more sources

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