Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature | BMC Ophthalmology | Full Text
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype | Semantic Scholar
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MELAS: a nationwide prospective cohort study of 96 patients in Japan. | Semantic Scholar
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity | Scientific Reports
Síndrome de MELAS (miopatía, encefalopatía, acidosis láctica y episodios semejantes a apoplejías)
Síndrome MELAS - Wikipedia, la enciclopedia libre
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Síndrome de MELAS: papel de la neuroimagen.
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Cerebral hyperperfusion and decreased cerebrovascular reactivity correlate with neurologic disease severity in MELAS - ScienceDirect
Revista Española de Cardiología
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Síndrome de MELAS (miopatía, encefalopatía, acidosis láctica y episodios semejantes a apoplejías)
Síndrome de MELAS: papel de la neuroimagen.
Síndrome de MELAS: síntomas, causas y tratamiento
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Síndrome de MELAS: papel de la neuroimagen.
Encefalomiopatía mitocondrial, acidosis láctica y episodios de accidente cerebrovascular, síndrome de MELAS. Reporte de un caso clínico
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