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Restrictive Cardiomyopathy

Annual Review of Medicine, 1984
Restrictive cardiomyopathy is a descriptive clinical and hemodynamic syndrome emphasizing the pathophysiologic mechanisms by which myocardial hypertrophy and/or infiltrative processes cause cardiocirculatory morbidity. This diagnosis can be made with precision only after pericardial construction is excluded and myocardial biopsy has identified the ...
J R, Benotti, W, Grossman
openaire   +3 more sources

Restrictive Cardiomyopathy in Childhood

Heart Failure Clinics, 2010
Depending on the part of the world one lives in, restrictive cardiomyopathy is either one of the rarest forms of cardiomyopathy in childhood, with no cause usually identified, or it is secondary to a poorly understood disease, endomyocardial fibrosis, that is endemic in some populations.
Susan Denfield
exaly   +3 more sources

Restrictive Cardiomyopathy

Pacing and Clinical Electrophysiology, 2009
Background: Restrictive cardiomyopathy is characterized by ventricular diastolic dysfunction with a clinical course in childhood that is often progressive despite medical therapy. Methods: A review of the literature and clinical experience was used to summarize the natural history of this oftentimes devastating disease with ...
Steven, Zangwill, Robert, Hamilton
openaire   +5 more sources

The Restrictive Cardiomyopathies

Cardiology Clinics, 1988
In parallel with the rapidly developing interest in the diastolic properties of ventricular function in the 1970s, the restrictive cardiomyopathies have taken their place as the third major category of primary heart muscle disease. The restrictive cardiomyopathies are characterized by primary abnormalities of diastolic ventricular function with normal ...
J S, Child, J K, Perloff
openaire   +2 more sources

Genetics of Restrictive Cardiomyopathy

Heart Failure Clinics, 2010
Restrictive physiology, a severe form of diastolic dysfunction, is characteristically observed in the setting of constrictive pericarditis and myocardial restriction. The latter is commonly due to systemic diseases, some of which are inherited as mendelian traits (eg, hereditary amyloidosis), while others are multifactorial (eg, sarcoidosis).
Petros Syrris
exaly   +3 more sources

Restrictive Cardiomyopathy

Cardiac CT, 2020
Learning objectives: To describe clinical and MR characteristics of different causes of restrictive cardiomyopathy with emphasis on specific features that may assist a radiologist in making correct differential diagnosis towards constrictive...
Xiao Li, Yining Wang
semanticscholar   +4 more sources

Restrictive cardiomyopathies

Current Opinion in Cardiology, 1994
Restrictive cardiomyopathy has always been a fairly common cause of cardiac death in the tropics through endomyocardial fibrosis. In temperate climates, amyloidosis is the most common form of the disease, whereas Löffler's endocarditis is quite rare. Amyloidosis is more frequently encountered as the population ages, but restrictive cardiomyopathy is ...
N, Spyrou, R, Foale
openaire   +2 more sources

Restrictive cardiomyopathy

Current Treatment Options in Cardiovascular Medicine, 2000
Of the three major functional categories of cardiomyopathies (dilated, hypertrophic, and restrictive), the restrictive cardiomyopathies (RCMs) are the least common in the Western world, but unfortunately often are associated with the greatest morbidity and mortality. Infiltrative disease of the myocardium (often caused by amyloidosis) is a common cause
, Artz, , Wynne
openaire   +2 more sources

Hemodynamics of constrictive pericarditis and restrictive cardiomyopathy

Catheterization and cardiovascular interventions, 2020
Constrictive pericarditis (CP) and restrictive cardiomyopathy (RCM) are indolent disabling diseases of diastolic function. The two conditions share common pathophysiologic features, resulting in similar and overlapping clinical presentations ...
J. Goldstein, M. Kern
semanticscholar   +1 more source

Restrictive cardiomyopathy

Medicine of Ukraine
The article deals with the classification, etiology, pathogenesis, clinic, diagnosis and treatment of restrictive cardiomyopathy (RCMD) as a wide range of diseases united by a single pathophysiological mechanism of restrictive diastolic dysfunction due to widespread fibrosis or infiltration of ventricular walls by various pathological substances.
О. A. Butko, K. Yu. Kinoshenko
  +6 more sources

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