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Frystyk J, Skjaerbaek C, Vestbo E, Fisker S, Orskov H
SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) (1517), an autosomal recessive disorder characterized by skeletal myopathy, progressive cardiomyopathy, hypoglycemia, and hyperammonemia
Insulin resistance and hyperinsulinaemia in the development and progression of cancer
In this brief review, we shall discuss recent important evidences of the potential clinical benefit of the incretin effect on cardiovascular system as well as the biological mechanisms, which underlie these effects
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