Gregory Mark Enns, MD is a Medical Geneticist (Genetic & Hereditary Disease Specialist) - Clinical Biochemical Genetics, Medical Geneticist - Clinical Genetics practicing in Stanford, CA
He has not ye… Read more ›
| University | Degree | Focus | Graduated |
|---|---|---|---|
| University of St. Andrews School of Medicine | Medical Degree | 1987 | |
| University of Glasgow Faculty of Medicine | Medical Degree | 1990 | |
| University of Glasgow Faculty of Medicine | Other Degree | 1990 |
| Institution | Focus | Year |
|---|---|---|
| Residency - Children'S Hospital Of L A, Pediatrics | Not Specified | |
| Residency - Children's Hospital Of L A | Not Specified | |
| Residency - Children's Hospital Program | Not Specified |
| Certification | Cert. Body | Year |
|---|---|---|
| Pediatrics | Pediatrics | Not Specified |
| Clinical Biochemical Genetics | Medical Genetics | Not Specified |
| Clinical Genetics (MD) | Medical Genetics | Not Specified |
| 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 |
Gregory Mark Enns, MD has not yet indicated the hospitals that he is affiliated with.
Clinical Biochemical Genetics; Clinical Genetics; Pediatrics
Years In Practice: 27 (started in 1997)
Accepts New Patients: Yes
