Gregory Enns
Academic Appointments
- Associate Professor - Med Center Line, Pediatrics - Genetics
Contact Information
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Clinical Offices
Medicine Specialties Clinic 730 Welch Rd 2nd Floor Palo Alto, CA 94304 Tel Work (650) 723-6858Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
Professional Snapshot
Clinical Focus
- Cancer Genetics
- Clinical Genetics
Professional Education
| Board Certification: | Clinical Genetics, American Board of Medical Genetics (1999) |
| Board Certification: | Clinical Biochemical Genetics, American Board of Medical Genetics (1999) |
| Fellowship: | UCSF Medical Center, CA (1998) |
| Residency: | Children's Hospital of Los Angeles, CA (1995) |
| Board Certification: | General Pediatrics, American Board of Pediatrics (1994) |
Postdoctoral Advisees
Graduate & Fellowship Program Affiliations
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industry partners. It is our policy to disclose payments of $5,000 or more, equity valued at $5,000 or more in a publicly traded company, or any equity in a privately held company, to physicians and scientists employed by Stanford University from companies or other commercial entities with which they interact as part of their professional activities. View Full Information
| Consulting: | Hall, Prangle & Schoonveld , Hyperion Therapeutics , MedaCorp , MediResources , StemCells, Inc. , University Hospitals |
| Equity: | StemCells, Inc. |
Scientific Focus
Current 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
- Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. N Engl J Med. 2007; (22): 2282-92
- Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load. Mol Genet Metab. 2006; (4): 364-71
- Postpartum "psychosis" in mild argininosuccinate synthetase deficiency. Obstet Gynecol. 2005; (5 Pt 2): 1244-6
- 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; (3): 417-20
- Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle. Clin Genet. 2005; (4): 337-48
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