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
- Academic Offices
Personal Information Email Tel (650) 498-5798 Tel (650) 723-6858Not for medical emergencies or patient use
Professional Overview
Clinical Focus
- Clinical Genetics
- Biochemical Genetics
- Mitochondrial Diseases
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 Advisee
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: | Mutual Insurance Co of AZ , Physician's Insurance , Seiller Waterman LLC , Simpson Healthcare Executives , StemCells, Inc. |
| Equity: | Gene Security Network , 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
- Nitrogen sparing therapy revisited 2009. Mol Genet Metab. 2010: S65-71
- Mapping gene associations in human mitochondria using clinical disease phenotypes. PLoS Comput Biol. 2009; (4): e1000374
- Novel deoxyguanosine kinase gene mutations and viral infection predispose apparently healthy children to fulminant liver failure. J Pediatr Gastroenterol Nutr. 2009; (1): 130-2
- Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia. Proc Natl Acad Sci U S A. 2009; (10): 3941-5
- Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. N Engl J Med. 2007; (22): 2282-92
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