Prevalence and natural history of heart disease in adults with primary mitochondrial respiratory chain disease-Reference-Cited by-同舟云学术

Prevalence and natural history of heart disease in adults with primary mitochondrial respiratory chain disease

Published:2010-01-18 Issue:2 Volume:12 Page:114-121
ISSN:1388-9842
Container-title:European Journal of Heart Failure
language:en
Short-container-title:European Journal of Heart Failure

Author:

Limongelli Giuseppe¹,Tome-Esteban Maite¹,Dejthevaporn Charungthai²,Rahman Shamima²,Hanna Michael G.²,Elliott Perry M.¹

Affiliation:

1. The Heart Hospital, University College London; 16-18 Westmoreland Street London W1G 8PH UK

2. MRC Centre for Neuromuscular Diseases; Institute of Neurology and The National Hospital for Neurology and Neurosurgery, Queen Square, University College London; London UK

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Mitochondrial respiratory-chain diseases;DiMauro;N Engl J Med,2003

2. New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation;Pulkes;Neuromuscul Disord,2005

3. Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases;Hanna;Cell Mol Life Sci,1999

4. Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy;Ino;Lancet,1991

5. Retrospective, multicentric study of 180 children with cytochrome C oxidase deficiency;Böhm;Pediatr Res,2006

Cited by 117 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Early cardiac mechanics abnormalities in patients with mitochondrial diseases;Mitochondrion;2024-09

2. Myoclonic Epilepsy With Ragged Red Fiber Cardiomyopathy: A Case Report and Brief Review of Literature;Cureus;2024-08-13

3. The Diagnostic and Therapeutic Implications of Phenocopies and Mimics of Hypertrophic Cardiomyopathy;Canadian Journal of Cardiology;2024-05

4. Hipertrofia ventricular izquierda. ¿Existe solo la miocardiopatía hipertrófica?;Archivos de Cardiología de México;2024-03-12

5. Case report: Clinical profile, molecular genetics, and neuroimaging findings presenting in a patient with Kearns-Sayre syndrome associated with inherited thrombophilia;Frontiers in Neurology;2024-01-05