Results 221 to 230 of about 38,525 (259)
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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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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.
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American Heart Journal, 1995
Congestive heart failure is an uncommon complication of pregnancy with potentially life-threatening consequences. Peripartum cardiomyopathy is a disease of unknown cause in which severe left ventricular dysfunction occurs during late pregnancy or the early puerperium.
M B, Lampert, R M, Lang
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Congestive heart failure is an uncommon complication of pregnancy with potentially life-threatening consequences. Peripartum cardiomyopathy is a disease of unknown cause in which severe left ventricular dysfunction occurs during late pregnancy or the early puerperium.
M B, Lampert, R M, Lang
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American Heart Journal, 1989
Diabetes mellitus is associated with an excessive cardiovascular morbidity and mortality. Although one frequently associates cardiac dysfunction with enhanced coronary atherosclerosis in diabetic patients, evidence has accumulated for the existence of a specific "diabetic" cardiomyopathy.
S W, Zarich, R W, Nesto
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Diabetes mellitus is associated with an excessive cardiovascular morbidity and mortality. Although one frequently associates cardiac dysfunction with enhanced coronary atherosclerosis in diabetic patients, evidence has accumulated for the existence of a specific "diabetic" cardiomyopathy.
S W, Zarich, R W, Nesto
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Digestive and Liver Disease, 2007
Decompensated liver cirrhosis is characterized by a peripheral vasodilation with a low-resistance hyperdynamic circulation. The sustained increase of cardiac work load associated with such a condition may result in an inconstant and often subclinical series of heart abnormalities, constituting a new clinical entity known as "cirrhotic cardiomyopathy ...
Milani, Alessandro +4 more
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Decompensated liver cirrhosis is characterized by a peripheral vasodilation with a low-resistance hyperdynamic circulation. The sustained increase of cardiac work load associated with such a condition may result in an inconstant and often subclinical series of heart abnormalities, constituting a new clinical entity known as "cirrhotic cardiomyopathy ...
Milani, Alessandro +4 more
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The Lancet, 2006
Peripartum cardiomyopathy (PPCM) is a disorder in which initial left ventricular systolic dysfunction and symptoms of heart failure occur between the late stages of pregnancy and the early postpartum period. It is common in some countries and rare in others. The causes and pathogenesis are poorly understood. Molecular markers of an inflammatory process
Karen, Sliwa, James, Fett, Uri, Elkayam
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Peripartum cardiomyopathy (PPCM) is a disorder in which initial left ventricular systolic dysfunction and symptoms of heart failure occur between the late stages of pregnancy and the early postpartum period. It is common in some countries and rare in others. The causes and pathogenesis are poorly understood. Molecular markers of an inflammatory process
Karen, Sliwa, James, Fett, Uri, Elkayam
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Pediatric Cardiology, 1995
An adolescent with mitochondrial cardiomyopathy is described. Skeletal and cardiac biopsies revealed abnormal mitochondria, with biochemical analysis showing cytochrome c oxidase deficiency.
J, Marin-Garcia, M J, Goldenthal
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An adolescent with mitochondrial cardiomyopathy is described. Skeletal and cardiac biopsies revealed abnormal mitochondria, with biochemical analysis showing cytochrome c oxidase deficiency.
J, Marin-Garcia, M J, Goldenthal
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[Cardiomyopathies. I: classification of cardiomyopathies--dilated cardiomyopathy].
Der Internist, 2006Cardiomyopathies are common causes of heart failure and sudden cardiac death. According to the WHO classification, "specific" cardiomyopathies are differentiated from "idiopathic" cardiomyopathies. Thus, this classification is primarily based on pathophysiological characteristics.
H P, Schultheiss +6 more
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Journal of the American Geriatrics Society, 1982
The literature on senile cardiomyopathy is selectively reviewed, information gained from the observation of more than 14,000 hearts at autopsy is presented, and suggestions for management of senile cardiomyopathy are given.
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The literature on senile cardiomyopathy is selectively reviewed, information gained from the observation of more than 14,000 hearts at autopsy is presented, and suggestions for management of senile cardiomyopathy are given.
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Infection, 1976
Fifty-one parasitic cardiomyopathies studied for periods ranging from 1 to 14 years were analyzed. In 32 cases chagasic etiology was demonstrated and in 19 cases toxoplasmic etiology. In the chagasic cases the diagnosis was confirmed by serological study and/or xenodiagnosis.
W, Apt, A, Arribada
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Fifty-one parasitic cardiomyopathies studied for periods ranging from 1 to 14 years were analyzed. In 32 cases chagasic etiology was demonstrated and in 19 cases toxoplasmic etiology. In the chagasic cases the diagnosis was confirmed by serological study and/or xenodiagnosis.
W, Apt, A, Arribada
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