MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case Report
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference15 articles.
1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome;Pavlakis;Ann Neurol,1984
2. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990
3. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome;Sproule;Ann N Y Acad Sci,2008
4. Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes;Chinnery;Brain,1997
5. Renal involvement in MELAS syndrome - a series of 5 cases and review of the literature;Seidowsky;Clin Nephrol,2013
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