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therefore, they are molecular targets for NAFLD or NASH therapy

If the forearm ischemic test result is abnormal (in line with glycolysis pathway enzymatic deficiencies), then genetic testing for McArdles disease is in order as the latter is the most common glycolytic pathway enzyme deficiency

S, soprattutto nella sua forma Acetil L-Carnitina , che attraversa facilmente la barriera emato-encefalica

J., Lafeber, H
