Education
He then completed a postdoctoral fellowship in the Department of Neurology at the University of Pennsylvania.
He then completed a postdoctoral fellowship in the Department of Neurology at the University of Pennsylvania.
His research focuses on genetic errors of energy metabolism and he defines disease entities using both biochemical and molecular approaches. As an "enzyme defect hunter", DiMauro has documented the molecular basis of many enzyme deficiencies, including carnitine palmitoyltransferase deficiency, the first error of fatty acid oxidation to be recognized in humans. He is a trustee on the United Mitochondrial Disease Foundation.
DiMauro has scores of publications.
He also has several books to his cartulary-register His last book is titled Mitochondrial Medicine and was published in 2006.