An Autopsy Case of Mitochondrial Encephalomyopathy (MELAS) with SpeciaI Reference to Extra-neuromuscular AbnormaIities
Author:
Publisher
Wiley
Subject
General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1827.1992.tb01883.x/fullpdf
Reference20 articles.
1. Mitochondrial en-cephalomyopathy: A group of neuromuscular disorders with defects in oxidative metabolism;Shapira;Isr J Med Sci,1977
2. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS): A distinctive clinical syndrome;Pavlakis;Ann Neurol,1984
3. A mito chondrial encephalomyopathy with cardiomyopathy: A case revealing a defect of complex I in the respiratory chain;Nishizawa;J Neurol Sci,1987
4. Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS);Yoneda;J Neurol Sci,1989
5. Widespread tissue distribution of a tRNALeu(uur) mutation in the mitochondrial DNA of a patient with MELAS syndrome;Ciafaloni;Neurology,1991
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2. A MELAS Patient Developing Fatal Acute Renal Failure with Lactic Acidosis and Rhabdomyolysis;Internal Medicine;2020-11-01
3. Clinical spectrum of the MELAS mutation in a large pedigree;Acta Neurologica Scandinavica;2009-01-29
4. Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNALeu(UUR) gene;Nephrology Dialysis Transplantation;2000-03-01
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