Rapid Progression of Cardiomyopathy in Mitochondrial Diabetes
Author:
Affiliation:
1. Divisions of Internal Medicine
2. Department of Medicine I, National Defense Medical College
3. Pathology, Tokyo Saiseikai Central Hospital
Publisher
Japanese Circulation Society
Subject
Cardiology and Cardiovascular Medicine,Physiology
Link
http://www.jstage.jst.go.jp/article/jcj/63/2/63_2_130/_pdf
Reference18 articles.
1. Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene
2. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
3. A mitochondrial encephalomyopathy with cardiomyopathy
4. Severe Mitochondrial Cardiomyopathy and Extraneuromuscular Abnormalities in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episode (MELAS)
5. Mitochondrial cytopathy.
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1. Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation;Nucleic Acids Research;2023-07-13
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4. A Case of Mitochondrial Cardiomyopathy Initially Diagnosed as Angina Pectoris with Hypertrophic Cardiomyopathy whose Electrocardiography Gradually Changed to Typical Mitochondrial Disease;Japanese Journal of Electrocardiology;2017
5. Treatment of Mitochondrial Diabetes with a Peroxisome Proliferator-activated Receptor (PPAR)-gamma Agonist;Internal Medicine;2016
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