Associate Professor, Molecular and Medical Genetics, Oregon Health and Science University School of Medicine
Medical Genetics
Dr. Cary O. Harding, MD
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Cary Harding is an expert in the field of Medical Genetics. He researched medicine at University of Washington School of Medicine. Dr. Cary O. Harding is a published doctor. He has 41 papers published. The most current publication "Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing."
Publications
- Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
- Glutamine and hyperammonemic crises in patients with urea cycle disorders.
- Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder.
- Single-dose, subcutaneous recombinant phenylalanine ammonia lyase conjugated with polyethylene glycol in adult patients with phenylketonuria: an open-label, multicentr...
- Fumarylacetoacetate hydrolase deficient pigs are a novel large animal model of metabolic liver disease.
- Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencies.
- Phenylketonuria Scientific Review Conference: State of the science and future research needs.
- Pharmacologic inhibition of L-tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU).
- Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening.
- Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on th...
- Seeking a cure for the royal pain.
- Altered Body Composition, and Energy Expenditure but Normal Glucose Tolerance among Humans with a Long-Chain Fatty Acid Oxidation Disorder.
- Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism.
- Ammonia Control in Children Ages 2 Months through 5 Years with Urea Cycle Disorders: Comparison of Sodium Phenylbutyrate and Glycerol Phenylbutyrate.
- In Vivo Selection of Transplanted Hepatocytes by Pharmacological Inhibition of Fumarylacetoacetate Hydrolase in Wild-type Mice.
- Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies.
- Substrate oxidation and cardiac performance during exercise in disorders of long chain fatty acid oxidation.
- Up to date knowledge on different treatment strategies for phenylketonuria.
- Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU).
- Siblings With Mitochondrial Acetoacetyl-CoA Thiolase Deficiency Not Identified by Newborn Screening.
- Prevalence and distribution of the c.1436C?T sequence variant of carnitine palmitoyltransferase 1A among Alaska Native infants.
- Hepatocyte-targeted HFE and TFR2 control hepcidin expression in mice.
- Comparison of adeno-associated virus pseudotype 1, 2, and 8 vectors administered by intramuscular injection in the treatment of murine phenylketonuria.
- Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium.
- NORMAL FATTY ACID CONCENTRATIONS IN YOUNG CHILDREN WITH PHENYLKETONURIA (PKU).
- EFFECT OF FEEDING, EXERCISE AND GENOTYPE ON PLASMA 3-HYDROXYACYLCARNITINES IN CHILDREN WITH LCHAD DEFICIENCY.
- Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiency.
- Correction of murine PKU following AAV-mediated intramuscular expression of a complete phenylalanine hydroxylating system.
- Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional ...
- Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunction...
- Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.
- Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene.
- Low therapeutic threshold for hepatocyte replacement in murine phenylketonuria.
- State-of-the-art 2003 on PKU gene therapy.
- The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuria.
- Potential for misdiagnosis due to lack of metabolic derangement in combined methylmalonic aciduria/hyperhomocysteinemia (cblC) in the neonate.
- Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
- L-2-oxothiazolidine-4-carboxylate supplementation in murine gamma-GT deficiency.
- Friedreich's ataxia associated with mitochondrial myopathy: clinicopathologic report.
- L-carnitine administration reduces number of episodes in cyclic vomiting syndrome.
Schools
University Of Washington School Of Medicine
University Of Wi Hospital and Cli
Doctors Specialties
- Clinical Biochemical Genetics
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
- Choice Plus POS II
- Altius Health Plans
- Amerigroup (Wellpoint)
- Blue Card PPO
- Blue Cross of Idaho PPO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Choice Health PPO
- First Health (Coventry Health Care) PPO
- Health Plan of Oregon PPO
- Medicare Advantage PFFS
- Kaiser Permanente
- Medicaid
- Medicare MCR
- ODS Health Plan
- Preferred PSN
- Heritage Plus
- Heritage Signature
- Personal Option EPO
- Preferred PPO
- Preferred Provider Network PPN
- Choice Plus POS
- Navigate POS
- Options PPO
- United Healthcare
Education
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University of Wisconsin -
University of Washington School of Medicine
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1952327926 |
| Last Name Of The Provider | HARDING |
| First Name Of The Provider | CARY |
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