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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
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity | Scientific Reports
Síndrome de MELAS: papel de la neuroimagen.
Síndrome MELAS - Wikipedia, la enciclopedia libre
Síndrome de MELAS: síntomas, causas y tratamiento
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MELAS: a nationwide prospective cohort study of 96 patients in Japan. | Semantic Scholar
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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PDF) Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype
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Encefalomiopatía mitocondrial, acidosis láctica y episodios de accidente cerebrovascular, síndrome de MELAS. Reporte de un caso clínico
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Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype | Semantic Scholar
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Food Selectivity of the Black Bullhead (Ictalurus melas, Rafinesque) in Lake Poinsett, South Dakota
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Síndrome de MELAS: papel de la neuroimagen.
A review of growth and life-history traits of native and non-native European populations of black bullhead Ameiurus melas – topic of research paper in Biological sciences. Download scholarly article PDF and read