Kidney involvement in MELAS syndrome: Description of 2 cases
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference29 articles.
1. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome;Sproule;Ann N Y Acad Sci,2008
2. Renal involvement in MELAS syndrome – a series of 5 cases and review of the literature;Seidowsky;Clin Nephrol,2013
3. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: an important cause of stroke in young people;Goodfellow;Postgrad Med J,2012
4. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA Leu (UUR) gene in Japanese patients with diabetes mellitus and end stage renal disease;Iwasaki;J Hum Genet,2001
5. Low prevalence of mitochondrial DNA 3243A>G point mutation in Caucasians with unexplained renal disease;Koshiyama;Diabet Med,2007
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