Results 281 to 290 of about 276,376 (316)
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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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Treatment of the cardiomyopathies
The American Journal of Cardiology, 1973The cardiomyopathies are defined as disorders of heart muscle of unknown cause and divided into three pathophysiologic groups: hypertrophic (obstructive) (synonymous with idiopathic hypertrophic subaortic stenosis), congestive and obliterative . Treatment is directed toward improvement in ventricular relaxation and compliance and removal of the ...
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Der Internist, 2006
This review focuses on hypertrophic (HCM), restrictive (RCM) and arrhythmogenic right ventricular cardiomyopathies (ARVC). The clinical phenotype of HCM depends not only on the gene mutations involved, but also on "modifier genes". It is characterized by an asymmetrical hypertrophy.
H-P, Schultheiss +6 more
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This review focuses on hypertrophic (HCM), restrictive (RCM) and arrhythmogenic right ventricular cardiomyopathies (ARVC). The clinical phenotype of HCM depends not only on the gene mutations involved, but also on "modifier genes". It is characterized by an asymmetrical hypertrophy.
H-P, Schultheiss +6 more
openaire +1 more source
2007
Regulation of Calcium (Ca) cycling by the sarcoplasmic reticulum (SR) underlies the control of cardiac contraction during excitation-contraction (E-C) coupling. Moreover, alterations in E-C coupling occurring in cardiac hypertrophy and heart failure are characterized by abnormal Ca-cycling through the SR network.
E G, Kranias, D M, Bers
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Regulation of Calcium (Ca) cycling by the sarcoplasmic reticulum (SR) underlies the control of cardiac contraction during excitation-contraction (E-C) coupling. Moreover, alterations in E-C coupling occurring in cardiac hypertrophy and heart failure are characterized by abnormal Ca-cycling through the SR network.
E G, Kranias, D M, Bers
openaire +2 more sources