Results 351 to 360 of about 269,027 (363)
Some of the next articles are maybe not open access.

Cardiomyopathy

2019
Hypertrophic cardiomyopathy (HCM) is characterized by the presence of increased left ventricular (LV) wall thickness that is not explained by loading conditions. The LV diastolic function is impaired in the majority of patients, and resting or provocable LV outflow tract obstruction is often present. The management of HCM is directed towards minimizing
openaire   +1 more source

Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies

Nature Reviews Cardiology, 2021
R. Walsh   +3 more
semanticscholar   +1 more source

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

Circulation, 1996
P. Richardson   +11 more
semanticscholar   +1 more source

Epidemiology of the inherited cardiomyopathies

Nature Reviews Cardiology, 2020
W. McKenna, D. Judge
semanticscholar   +1 more source

Dilated cardiomyopathy

2013
Epidemiology, aetiology, pathophysiology, diagnosis, and therapy of patients with dilated cardiomyopathy are discussed. Recommendations on the use of CRT and ICD therapy by the ACC/AHA and ESC are presented.
Demosthenes G. Katritsis   +2 more
openaire   +1 more source

Cardiomyopathies

Science, 1967
E, Bajusz, F, Homburger
openaire   +2 more sources

Cardiomyopathy

BMJ, 2009
Liana, Daley   +3 more
openaire   +2 more sources

Alcoholic cardiomyopathy

The American Journal of Cardiology, 1968
G E, Burch, N P, DePasquale
openaire   +3 more sources

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