scholarly journals Heart Failure Association of the ESC, Heart Failure Society of America and Japanese Heart Failure Society Position statement on endomyocardial biopsy

2021 ◽  
Author(s):  
Petar M. Seferović ◽  
Hiroyuki Tsutsui ◽  
Dennis M. McNamara ◽  
Arsen D. Ristić ◽  
Cristina Basso ◽  
...  
Keyword(s):  
Heart Failure ◽  
Endomyocardial Biopsy ◽  
Position Statement

American association of heart failure nurses (AAHFN) position statement on patient access to healthcare

Heart & Lung ◽  
2017 ◽  
Vol 46 (3) ◽  
pp. 209-210
Author(s):  
Marilyn A. Prasun ◽  
Elizabeth Bolton-Harris ◽  
Kimberly Nelson ◽  
Sita Price ◽  
Kelly D. Stamp ◽  
...  
Keyword(s):  
Heart Failure ◽  
American Association ◽  
Position Statement ◽  
Access To Healthcare ◽  
Patient Access

The incidence of myocarditis in endomyocardial biopsy samples from patients with congestive heart failure

1990 ◽  
Vol 120 (6) ◽  
pp. 1370-1377 ◽  
Author(s):  
Jovan D. Vasiljevic ◽  
Vladimir Kanjuh ◽  
Petar Seferovic ◽  
Mihajlo Sesto ◽  
Djurica Stojsic ◽  
...  
Keyword(s):  
Heart Failure ◽  
Congestive Heart Failure ◽  
Endomyocardial Biopsy

An X-Linked Recessive Cardiomyopathy with Abnormal Mitochondria

PEDIATRICS ◽  
1979 ◽  
Vol 64 (1) ◽  
pp. 24-29 ◽  
Author(s):  
Harry B. Neustein ◽  
Paul R. Lurie ◽  
Beverly Dahms ◽  
Masato Takahashi
Keyword(s):  
Electron Microscopy ◽  
Heart Failure ◽  
Congestive Heart Failure ◽  
Cardiac Disease ◽  
Endomyocardial Biopsy ◽  
Skeletal Muscles ◽  
Chronic Congestive Heart Failure ◽  
Family Pedigree ◽  
Liver And Kidney ◽  
Abnormal Mitochondria

A transvascular endomyocardial biopsy from an infant with cardiomyopathy and chronic congestive heart failure showed abnormal mitochondria when examined by electron microscopy. At necropsy, similar abnormal mitochondria were seen in skeletal muscles, liver, and kidney. The patient's family pedigree revealed several male babies who had cardiac disease and died in infancy. Myocardium obtained at necropsy from three cousins contained mitochondria with abnormalities similar to those from the proband. An X-linked recessive cardiomyopathy seems likely in this family.

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