Teresa D. Douglas, Ph.D.
Affiliations: | 2012 | Biological and Biomedical Sciences | Emory University, Atlanta, GA |
Area:
Nutrition, Neuroscience BiologyGoogle:
"Teresa Douglas"Mean distance: 35622
Parents
Sign in to add mentor| Rani H. Singh | grad student | 2012 | Emory | |
| (Impact of sapropterin (tetrahydrobiopterin, BH4) treatment, with and without diet liberalization, on monoamine status and quality of life in a phenylketonuria (PKU) cohort.) | ||||
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| Douglas TD, Newby LK, Eckstrand J, et al. (2020) Lipid changes in the metabolome of a single case study with maple syrup urine disease (MSUD) after five days of improved diet adherence of controlled branched-chain amino acids (BCAA). Molecular Genetics and Metabolism Reports. 25: 100651 |
| Douglas TD, Nucci AM, Berry AM, et al. (2019) Large neutral amino acid status in association with P:T ratio and diet in adult and pediatric patients with phenylketonuria. Jimd Reports. 50: 50-59 |
| Douglas T, Singh R. (2019) Elevated Urine Creatinine in Relation to Protein Intake in Adolescent and Adult Females with Phenylketonuria (PKU) with Comparison to NHANES (P08-060-19) Current Developments in Nutrition. 3 |
| Brantley KD, Douglas TD, Singh RH. (2018) One-year follow-up of B vitamin and Iron status in patients with phenylketonuria provided tetrahydrobiopterin (BH4). Orphanet Journal of Rare Diseases. 13: 192 |
| Jani R, Coakley K, Douglas T, et al. (2017) Protein intake and physical activity are associated with body composition in individuals with phenylalanine hydroxylase deficiency. Molecular Genetics and Metabolism |
| Singh RH, Cunningham AC, Mofidi S, et al. (2016) Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach. Molecular Genetics and Metabolism |
| Coakley KE, Douglas TD, Goodman M, et al. (2016) Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency. Journal of Inherited Metabolic Disease. 39: 363-72 |
| Coakley KE, Douglas TD, Goodman M, et al. (2016) Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency Journal of Inherited Metabolic Disease. 1-10 |
| Coakley K, Douglas T, Singh R. (2014) Phenylketonuria is a condition of inflammation associated with high BMI and low bone turnover (1034.2) The Faseb Journal. 28 |
| Douglas TD, Ramakrishnan U, Kable JA, et al. (2013) Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride. Health and Quality of Life Outcomes. 11: 218 |