Dr. Cary Owen Harding MD
Geneticist | Clinical Biochemical Genetics
3181 Sw Sam Jackson Park Rd Portland OR, 97239About
Dr. Cary Harding practices Genetic Medicine in Portland, OR. As a geneticist, Dr. Harding performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Harding carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Univ of Wa Sch of Med, Seattle Wa 1987
University of Washington School of Medicine 1987
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- gamma-Glutamyl transferase (GGT) deficiency in the GGTenu1 mouse results from a single point mutation that leads to a stop codon in the first coding exon of GGT mRNA.
- 'Mommy, why can't I have a hamburger like the other kids?'.
- L-2-oxothiazolidine-4-carboxylate supplementation in murine gamma-GT deficiency.
- Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
- Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.
- sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis.
- State-of-the-art 2003 on PKU gene therapy.
- The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuria.
- Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia.
- Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene.
- Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.
- Low therapeutic threshold for hepatocyte replacement in murine phenylketonuria.
- Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.
- 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 protein (TFP) deficiency.
- The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.
Clinical Trials
Treatments
- Birth Defects
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