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Síndrome de MELAS: papel de la neuroimagen.
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Different mitochondrial genetic defects exhibit the same protein signature of metabolism in skeletal muscle of PEO and MELAS patients: A role for oxidative stress - ScienceDirect
Síndrome de MELAS: papel de la neuroimagen.
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) | Radiology Reference Article | Radiopaedia.org
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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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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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Síndrome de MELAS (miopatía, encefalopatía, acidosis láctica y episodios semejantes a apoplejías)
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PDF) Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype