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Melas: aproximación diagnóstica y experiencia terapéutica r..:

Patiño, Mauricio ; Palacios Sánchez, Eduardo
Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol. 1984;16:481-8. 2. Chinnery PF, Tumban DM. Epidemiology and treatment of mitochondrial disorders. Am J Med Genet. 2001;106:94-101. 3. Gerbitz K-D, van den Ouweland JMW, Maassen JA, Jaksch M. Mitochondrial diabetes mellitus: a review. Biochim Biophys Acta.1995;1271:253-60. 4. Uusimaa J, Moilanen JS, Vainionpaa L, et al. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children. Ann Neurol. 2007; 62:278-87. 5. Manwaring N, Jones MM, Wang JJ, et al. Population prevalence of the MELAS A3243G mutation. Mitochondrion. 2007;7:230-3. 6. Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann N Y Acad Sci. 2008;1142:133-58. 7. Schon EA. ....  , 2022