Cardiac Dysfunction in Mitochondrial Disease-Reference-Cited by-同舟云学术

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Cardiac Dysfunction in Mitochondrial Disease

Published:2013 Issue:11 Volume:77 Page:2799-2806
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Villar Pedro¹²,Bretón Begoña¹²,García-Pavía Pablo³⁴²,González-Páramos Cristina⁵,Blázquez Alberto⁶⁷⁸,Gómez-Bueno Manuel³⁴²,García-Silva Teresa⁷⁹,García-Consuegra Ines⁷⁸,Martín Miguel Angel⁶⁷⁸,Garesse Rafael⁵⁶⁷,Bornstein Belen⁵⁶⁷¹²,Gallardo M. Esther⁵⁶⁷

Affiliation:

1. Biochemistry Unit, “Hospital Universitario Puerta de Hierro”

2. Research Institute “Puerta de Hierro” Majadahonda (IDIPHIM)

3. Cardiology Unit, “Hospital Universitario Puerta de Hierro”

4. Net of Clinical and Basic Research in Heart Failure (REDINSCOR)

5. Biochemistry Departament, Biomedical Research Institute “Alberto Sols”, Medicine College, UAM-CSIC

6. Rare Diseases Biomedical Research Centre (CIBERER)

7. Health Research Institute “Hospital 12 de Octubre (i+12)”

8. Laboratory of Mitochondrial Diseases, Research Centre

9. Pediatrics Unit, “Hospital Universitario 12 de Octubre”

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/circj/77/11/77_CJ-13-0557/_pdf

Reference50 articles.

1. 1. Lev D, Nissenkorn A, Leshinsky-Silver E, Sadeh M, Zeharia A, Garty BZ, et al. Clinical presentations of mitochondrial cardiomyopathies. Pediatr Cardiol 2004; 25: 443–450.

2. 2. Kimura A. Contribution of genetic factors to the pathogenesis of dilated cardiomyopathy: The cause of dilated cardiomyopathy: Genetic or acquired? (genetic-side). Circ J 2011; 75: 1756–1765; discussion 1765.

3. 3. Paterick TE, Tajik AJ. Left ventricular noncompaction: A diagnostically challenging cardiomyopathy. Circ J 2012; 76: 1556–1562.

4. 4. Bates MG, Bourke JP, Giordano C, d’Amati G, Turnbull DM, Taylor RW. Cardiac involvement in mitochondrial DNA disease: Clinical spectrum, diagnosis, and management. Eur Heart J 2012; 33: 3023–3033.

5. 5. Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, et al. Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA(Leu)(UUR). Lancet 1991; 338: 143–147.

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