Gregory Mark Enns, MD
Medical Geneticist/Genomicist - Clinical Genetics and Genomics (MD), Medical Geneticist/Genomicist - Clinical Biochemical Genetics
Highlights
- Board Certified
Biography
Gregory Mark Enns, MD is a Medical Geneticist/Genomicist - Clinical Genetics and Genomics (MD), Medical Geneticist/Genomicist - Clinical Biochemical Genetics practicing in Stanford, CA
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Summary
Provider Training
| University | Degree | Focus | Graduated |
|---|---|---|---|
| University of St. Andrews School of Medicine | Medical Degree | 1987 | |
| University of Glasgow Faculty of Medicine | Other Degree | 1990 | |
| University of Glasgow Faculty of Medicine | Medical Degree | 1990 |
| Institution | Focus | Year |
|---|---|---|
| Residency - Children's Hospital Program | Not Specified | |
| Residency - Children's Hospital Of L A | Not Specified | |
| Residency - Children'S Hospital Of L A, Pediatrics | Not Specified |
| Certification | Cert. Body | Year |
|---|---|---|
| Clinical Biochemical Genetics | Medical Genetics | Not Specified |
| Clinical Genetics (MD) | Medical Genetics | Not Specified |
| Pediatrics | Pediatrics | Not Specified |
Experience & Accolades
| Publication | Publisher | Title | Published |
|---|---|---|---|
| Other Publication | Jourl of chromatography. B, Alytical technologies in the biomedical an | A new LC-MS/MS method for the clinical determition of reduced and oxidized glutathione from whole | 2013 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Brain uptake of Tc99m | 2012 |
| Other Publication | MITOCHONDRION | Leigh syndrome caused by a novel m.4296G > A mutation in mitochondrial tR isoleucine | 2012 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Initial experience in the treatment of inherited mitochondrial disease with EPI-743 | 2012 |
| Other Publication | PROCEEDINGS OF THE TIOL ACADEMY OF SCIENCES OF THE UNITED STATES OF AM | High-quality D sequence capture of 524 disease candidate genes | 2011 |
| Other Publication | JOURL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION | Novel Deoxyguanosine Kise Gene Mutations | 2009 |
| Other Publication | PLOS COMPUTATIOL BIOLOGY | Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes | 2009 |
| Other Publication | PROCEEDINGS OF THE TIOL ACADEMY OF SCIENCES OF THE UNITED STATES OF AM | Inherited disorders affecting mitochondrial function are associated with glutathione deficiency | 2009 |
| Other Publication | NEW ENGLAND JOURL OF MEDICINE | Survival after treatment with phenylacetate and benzoate for urea-cycle disorders | 2007 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Molecular-clinical correlations in a family with variable tissue mitochondrial D T8993G mutant load | 2006 |
| Other Publication | CLINICAL GENETICS | Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities | 2005 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | The contribution of mitochondria to common disorders | 2003 |
| Other Publication | JOURL OF PEDIATRICS | Mitochondrial respiratory chain complex I deficiency with clinical | 2000 |
| Other Publication | PEDIATRIC TRANSPLANTATION | Liver transplantation for urea cycle disorders in pediatric patients: A single-center experience | 2013 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS PART A | Atypical Amyoplasia Congenita in an Infant With Leigh Syndrome | 2012 |
| Other Publication | PEDIATRIC TRANSPLANTATION | Propionic acidemia: To liver transplant or not to liver transplant? | 2012 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | tural history of propionic acidemia | 2012 |
| Other Publication | PSYCHOPHARMACOLOGY | Length of pretal exposure to selective serotonin reuptake inhibitor (SSRI) antidepressants | 2011 |
| Other Publication | BIOORGANIC & MEDICIL CHEMISTRY LETTERS | alpha-Tocotrienol quinone modulates oxidative stress response and the biochemistry of aging | 2011 |
| Other Publication | Niemi, A. K., Cusmano-Ozog, K., Rosenblatt, D. S., Enns, G. M. | Long-term follow-up of a patient with early onset CBLG disease | 2011 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Suboptimal outcomes in patients with PKU treated early with diet alone: Revisiting the evidence | 2010 |
| Other Publication | PEDIATRIC TRANSPLANTATION | Long-term outcome following pediatric liver transplantation for metabolic disorders | 2010 |
| Other Publication | Enns, G. M. | Nitrogen sparing therapy revisited 2009 | 2010 |
| Other Publication | BONE MARROW TRANSPLANTATION | Pathological evidence of Wolman's dise | 2009 |
| Other Publication | JOURL OF PEDIATRIC HEMATOLOGY ONCOLOGY | Hypoplastic Glomerulocystic Kidney Disease | 2009 |
| Other Publication | CLINICAL NEUROPATHOLOGY | A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy | 2009 |
| Other Publication | JOURL OF PERITOLOGY | Successful pregncy and cesarean delivery via noninvasive ventilation in mitochondrial myopathy | 2009 |
| Other Publication | SEMIRS IN PEDIATRIC NEUROLOGY | Neurologic Damage and Neurocognitive Dysfunction in Urea Cycle Disorders | 2008 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Cell-based therapies for metabolic liver disease | 2008 |
| Other Publication | NEUROSURGICAL FOCUS | Central nervous system therapy for lysosomal storage disorders | 2008 |
| Other Publication | JOURL OF NEUROSURGERY | Glutaric acidemia type I: a neurosurgical perspective | 2007 |
| Other Publication | PEDIATRICS | Systemic hyalinosis: A distinctive early childhood | 2006 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS PART A | Genitopatellar syndrome: Expanding the phenotype and excluding mutations in LMX1B and TBX4 | 2006 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Glutaryl-CoA dehydrogese deficiency and newborn screening | 2005 |
| Other Publication | JOURL OF INHERITED METABOLIC DISEASE | Magement of methylmalonic acidaemia by combined liver-kidney transplantation | 2005 |
| Other Publication | OBSTETRICS AND GYNECOLOGY | Postpartum psychosis in mild argininosuccite synthetase deficiency | 2005 |
| Other Publication | BIOLOGICAL CHEMISTRY | Identification of three novel mutations | 2005 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS PART A | Mild developmental delay in termil chromosome 6p deletion | 2004 |
| Other Publication | PEDIATRICS | Termil 22q deletion syndrome | 2004 |
| Other Publication | JOURL OF INHERITED METABOLIC DISEASE | Head imaging abnormalities in dihydropyrimidine dehydrogese deficiency | 2004 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS PART A | Methotrexate/misoprostol embryopathy: Report of four cases resulting from failed medical abortion | 2003 |
| Other Publication | JOURL OF MEDICAL GENETICS | Compensatory amplification of mtD in a patient with a novel deletion | 2003 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Congenital disorder of glycosylation Ic in patients of Indian origin | 2003 |
| Other Publication | JOURL OF PEDIATRICS | Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 | 2002 |
| Other Publication | Adolescent medicine (Philadelphia, Pa.) | The adolescent with an inborn error of metabolism: medical issues and transition to adulthood. | 2002 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Early neotal diagnosis of long-chain 3-hydroxyacyl coenzyme A dehydrogese | 2002 |
| Other Publication | MOLECULAR GENETICS AND METABOLISM | Functiol alysis of novel mutations | 2001 |
| Other Publication | JOURL OF INHERITED METABOLIC DISEASE | Clinical course and biochemistry of sialuria | 2001 |
| Other Publication | PEDIATRIC RESEARCH | Molecular correlations in phenylketonuria | 1999 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS | Apparent cyclophosphamide (cytoxan) embryopathy: A distinct phenotype? | 1999 |
| Other Publication | JOURL OF INHERITED METABOLIC DISEASE | Progressive neurological deterioration | 1999 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS | Severe congenital anomalies requiring transplantation in children with Kabuki syndrome | 1998 |
| Other Publication | AMERICAN JOURL OF MEDICAL GENETICS | Congenital diaphragmatic defects and associated syndromes, malformations | 1998 |
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Specialties
Languages Spoken
EnglishMedical Specialties
- Medical Geneticist/Genomicist - Sub-Specialty: Clinical Genetics and Genomics (MD)
- Medical Geneticist/Genomicist - Sub-Specialty: Clinical Biochemical Genetics
Clinical Biochemical Genetics; Clinical Genetics; Pediatrics
Years In Practice: 29 (started in 1997)
Accepts New Patients: Yes
Payment Options
Payment DetailsReviews
Average Rating:
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Locations
Affiliated Practices
Dr. Gregory Enns, MD
300 Pasteur Dr, H315Stanford, CA 94305
Lucile Packard Childrens Hospital Stanford
725 Welch RdPalo Alto, CA 94304
Practice
300 Pasteur Dr, H315Palo Alto, CA 94305
Practice Colleagues
Erica Knowles, NP - Nurse Practitioner
Anna Michel Olsen, - Anesthesiologist, Student
Laura Prolo, MD, PhD - Neurological Surgeon
Kathleen Guglielmino, MD - Hospitalist, Pediatrician
Kimberly Trujillo, MD, MPH - Pediatrician
Susan Schelley, MPH - Medical Geneticist/Genomicist
Stephanie Tran, MD - Student
Jason Reminick, MD, MBA - Student
Anuradha Gorukanti, MD - Pediatrician
Brindha Saravanabavanandhan, MD - Obstetrician/Gynecologist
Procedures & Services
Procedures & Treatments Offered
- Birth Defects
- Epilepsy
- Heart Disease
- Learning Disabilities
Commonly Prescribed Medications
Gregory Mark Enns, MD has not yet listed the medications that he commonly prescribes.
Accepted Insurance
Accepted Insurance
Gregory Mark Enns, MD has not yet specified the insurance plans he accepts.