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1. Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate1. Issue 6 (3rd January 2013)

2. Autologous Gene and Cell Therapy Provides Safe and Long-Term Curative Therapy in A Large Pig Model of Hereditary Tyrosinemia Type 1. Issue 1 (January 2019)

3. Cardiac tissue citric acid cycle intermediates in exercised very long‐chain acyl‐CoA dehydrogenase‐deficient mice fed triheptanoin or medium‐chain triglyceride. Issue 6 (4th August 2020)

4. Generating a taxonomy for genetic conditions relevant to reproductive planning. Issue 3 (March 2016)

5. Higher dietary protein intake preserves lean body mass, lowers liver lipid deposition, and maintains metabolic control in participants with long‐chain fatty acid oxidation disorders. Issue 5 (24th July 2019)

7. Pharmacokinetic, pharmacodynamic, and immunogenic rationale for optimal dosing of pegvaliase, a PEGylated bacterial enzyme, in adult patients with phenylketonuria. Issue 5 (31st May 2021)