Results 271 to 280 of about 347,198 (324)
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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
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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
+7 more sources
Revista Española de Cardiología, 2022
INTRODUCTION AND OBJECTIVES Missense mutations in the filamin C (FLNC) gene have been reported as cause of inherited cardiomyopathy. Knowledge of the pathogenicity and genotype-phenotype correlation remains scarce.
F. Bermúdez-Jiménez +19 more
semanticscholar +1 more source
INTRODUCTION AND OBJECTIVES Missense mutations in the filamin C (FLNC) gene have been reported as cause of inherited cardiomyopathy. Knowledge of the pathogenicity and genotype-phenotype correlation remains scarce.
F. Bermúdez-Jiménez +19 more
semanticscholar +1 more source
HeartMate 3 Implantation Through Left Atrial e-PTFE Conduit for Restrictive Cardiomyopathy
Annals of Thoracic Surgery Short Reports, 2022Restrictive or hypertrophic cardiomyopathy presents a challenge to left ventricular assist device placement because of the small left ventricle cavity.
Aaron Guo +7 more
semanticscholar +1 more source
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
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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
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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
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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
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The Restrictive Cardiomyopathies
Cardiology Clinics, 1988In 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
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, 2011 Restrictive cardiomyopathy is a condition characterized by normal left ventricular cavity size and systolic function but with increased myocardial stiffness [1]. This makes the ventricle incompliant and fi ll predominantly in early diastole.
Michael Y. Henein, Mary Sheppard
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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
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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
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FAMILIAL RESTRICTIVE CARDIOMYOPATHY
Australian and New Zealand Journal of Medicine, 1988Abstract:The cases of a father and daughter with idiopathic restrictive cardiomyopathy are described. In contrast to other forms of cardiomyopathy, this type is rarely familial.
Aroney, C, Bett, N, Radford, D
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Restrictive Cardiomyopathy in Childhood
Heart Failure Clinics, 2010Depending 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 W, Denfield, Steven A, Webber
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