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Above, we have summarized the existing research on mitophagy and microvascular complications in diabetes

Adamczak DM, Oduah MT, Kiebalo T, Nartowicz S, Bben M, Pochylski M, Ciepucha A, Gwizdaa A, Lesiak M, Straburzyska-Migaj E

Given the observed changes in the respiratory quotient and perceived exertion, further studies could also explore the underlying biochemical mechanisms responsible for these effects, such as the role of L-carnitine in mitochondrial function, fat oxidation, and glycogen preservation during prolonged exercise

95% CI, 0.87-0.94), as were the risks for chronic kidney disease (HR = 0.97

Disorders of organic acid metabolism Methylmalonic acidemia Methylmalonic acidemia (MMA) is an autosomal recessive disorder caused by a deficiency in methylmalonyl coenzyme A (CoA) mutase (MUT), which is encoded by the MUT gene

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