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Gregory EnnsAcademic Appointments
Appointment
Organization
Associate Professor - Med Center Line
Genetics ;
Pediatrics ;
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Professional Education
Degree
Awarding Institution
Field of Study
Year of Graduation
MB, ChB
University of Glasgow
Medicine
1990
Diploma, Medical Science
University of St. Andrews
Medicine
1987
BA
Pomona College
Biology
1984
Research Interests
Research interests include novel means of diagnosing and treating mitochondrial disorders, with an emphasis on antioxidant therapy, lysosomal disorders, and newborn screening by tandem mass spectrometry. Current pursuits include the analysis of glutathione and antioxidant status in patients who have mitochondrial disorders and the development of new techniques for diagnosing these conditions.
Publications
- Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A "Survival after treatment with phenylacetate and benzoate for urea-cycle disorders." N Engl J Med 2007; 356: 22: 2282-92 More »
- Enns GM, Bai RK, Beck AE, Wong LJ "Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load." Mol Genet Metab 2006; More »
- Enns GM, O'brien WE, Kobayashi K, Shinzawa H, Pellegrino JE "Postpartum "psychosis" in mild argininosuccinate synthetase deficiency." Obstet Gynecol 2005; 105: 5: 1244-6 More »
- Enns G, Hoppel C, Dearmond S, Schelley S, Bass N, Weisiger K, Horoupian D, Packman S "Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle." Clin Genet 2005; 68: 4: 337-48 More »
- Gallagher RC, Cowan TM, Goodman SI, Enns GM "Glutaryl-CoA dehydrogenase deficiency and newborn screening: Retrospective analysis of a low excretor provides further evidence that some cases may be missed." Mol Genet Metab 2005; More »
21 publications: view full list
