Hypertrophic cardiomyopathy in mitochondrial disorders: description of an uncommon clinical case-Reference-Cited by-同舟云学术

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Hypertrophic cardiomyopathy in mitochondrial disorders: description of an uncommon clinical case

Published:2017-06-06 Issue:9 Volume:19 Page:1201-1204
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:Eur J Heart Fail

Author:

Marsico Fabio¹,D'Andrea Claudia¹,Parente Antonio¹,De Martino Fabiana¹,Capasso Letizia²,Raimondi Francesco²,Paolillo Stefania³,Dellegrottaglie Santo⁴,Marciano Caterina⁵,Trimarco Bruno¹,Perrone Filardi Pasquale¹

Affiliation:

1. Department of Advanced Biomedical Sciences; University of Naples Federico II; Naples Italy

2. Department of Translational Medical Sciences; University of Naples Federico II; Naples Italy

3. IRCCS SDN; Istituto di Ricerca; Naples Italy

4. Villa dei Fiori; Acerra; Naples Italy

5. Istituto Diagnostico Varelli; Naples Italy

Funder

Cardiovascular Pathophysiology and Therapeutics PhD programme of the University of Naples Federico II

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Cardiological manifestations of mitochondrial respiratory chain disorders;Berardo;Acta Myol,2011

2. The genetics and pathology of oxidative phosphorylation;Smeitink;Nat Rev Genet,2001

3. Identification of a Ca2+-ATPase in brown adipose tissue mitochondria: regulation of thermogenesis by ATP and Ca2+;Meis;J Biol Chem,2006

4. Mito-mice: animal models for mitochondrial DNA-based diseases;Nakada;Semin Cell Dev Biol,2001

5. Cardiomyopathy in children with mitochondrial disease. Clinical course and cardiological findings;Holmgren;Eur Heart J,2003

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