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Archives of Gynecology and Obstetrics, 2009
According to current definition, peripartum cardiomyopathy (PPCM) is a rare disorder in which left ventricular dysfunction and symptoms of heart failure occur in the last month of pregnancy. It has been reported that the incidence of PPCM is 1 in 3,000-4,000 live births.
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According to current definition, peripartum cardiomyopathy (PPCM) is a rare disorder in which left ventricular dysfunction and symptoms of heart failure occur in the last month of pregnancy. It has been reported that the incidence of PPCM is 1 in 3,000-4,000 live births.
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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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International Journal of Cardiology, 2006
Recently, many reports have been published about apical ballooning or takotsubo cardiomyopathy. This disease is a new entity of acute reversible heart failure. Abnormal catecholamine dynamics due to stress may be the primary cause of this condition.
Yoshihiro J, Akashi, Stefan D, Anker
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Recently, many reports have been published about apical ballooning or takotsubo cardiomyopathy. This disease is a new entity of acute reversible heart failure. Abnormal catecholamine dynamics due to stress may be the primary cause of this condition.
Yoshihiro J, Akashi, Stefan D, Anker
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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
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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
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Current Treatment Options in Cardiovascular Medicine, 2001
The management of patients with dilated cardiomyopathy (DCM) heart failure starts with the determination of the underlying diagnosis, definition of the hemodynamic character (eg, systolic, diastolic, valvular, right- and left-sided heart dysfunction), recognition of complicating factors (eg, atrial fibrillation, renal dysfunction), and consideration ...
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The management of patients with dilated cardiomyopathy (DCM) heart failure starts with the determination of the underlying diagnosis, definition of the hemodynamic character (eg, systolic, diastolic, valvular, right- and left-sided heart dysfunction), recognition of complicating factors (eg, atrial fibrillation, renal dysfunction), and consideration ...
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