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Síndrome de MELAS (miopatía, encefalopatía, acidosis láctica y episodios semejantes a apoplejías)
Síndrome de MELAS: papel de la neuroimagen.
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Mitochondrial 3243A > G mutation confers pro-atherogenic and pro-inflammatory properties in MELAS iPS derived endothelial cells | Cell Death & Disease
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
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MELAS: a nationwide prospective cohort study of 96 patients in Japan. | Semantic Scholar
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Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype | Semantic Scholar
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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
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) | Radiology Reference Article | Radiopaedia.org
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
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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