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Teresa D. Douglas, Ph.D. - Publications

Affiliations: 
2012 Biological and Biomedical Sciences Emory University, Atlanta, GA 
Area:
Nutrition, Neuroscience Biology
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14/17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Douglas TD, Newby LK, Eckstrand J, Wixted D, Singh RH. 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. PMID 33088714 DOI: 10.1016/j.ymgmr.2020.100651  0.482
2019 Douglas TD, Nucci AM, Berry AM, Henes ST, Singh RH. 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. PMID 31741827 DOI: 10.1002/jmd2.12076  0.539
2019 Douglas T, Singh R. 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. DOI: 10.1093/cdn/nzz044.p08-060-19  0.565
2018 Brantley KD, Douglas TD, Singh RH. One-year follow-up of B vitamin and Iron status in patients with phenylketonuria provided tetrahydrobiopterin (BH4). Orphanet Journal of Rare Diseases. 13: 192. PMID 30373601 DOI: 10.1186/S13023-018-0923-2  0.57
2017 Jani R, Coakley K, Douglas T, Singh R. Protein intake and physical activity are associated with body composition in individuals with phenylalanine hydroxylase deficiency. Molecular Genetics and Metabolism. PMID 28465125 DOI: 10.1016/J.Ymgme.2017.04.012  0.612
2016 Singh RH, Cunningham AC, Mofidi S, Douglas TD, Frazier DM, Hook DG, Jeffers L, McCune H, Moseley KD, Ogata B, Pendyal S, Skrabal J, Splett PL, Stembridge A, Wessel A, et al. Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach. Molecular Genetics and Metabolism. PMID 27211276 DOI: 10.1016/J.Ymgme.2016.04.008  0.52
2016 Coakley KE, Douglas TD, Goodman M, Ramakrishnan U, Dobrowolski SF, Singh RH. Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency. Journal of Inherited Metabolic Disease. 39: 363-72. PMID 26883219 DOI: 10.1007/S10545-015-9910-0  0.593
2016 Coakley KE, Douglas TD, Goodman M, Ramakrishnan U, Dobrowolski SF, Singh RH. Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency Journal of Inherited Metabolic Disease. 1-10. DOI: 10.1007/s10545-015-9910-0  0.484
2014 Coakley K, Douglas T, Singh R. Phenylketonuria is a condition of inflammation associated with high BMI and low bone turnover (1034.2) The Faseb Journal. 28. DOI: 10.1096/Fasebj.28.1_Supplement.1034.2  0.573
2013 Douglas TD, Ramakrishnan U, Kable JA, Singh RH. Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride. Health and Quality of Life Outcomes. 11: 218. PMID 24373161 DOI: 10.1186/1477-7525-11-218  0.57
2013 Douglas TD, Jinnah HA, Bernhard D, Singh RH. The effects of sapropterin on urinary monoamine metabolites in phenylketonuria. Molecular Genetics and Metabolism. 109: 243-50. PMID 23712020 DOI: 10.1016/J.Ymgme.2013.04.017  0.529
2013 Douglas TD, Kennedy MJ, Quirk ME, Yi SH, Singh RH. Accuracy of six anthropometric skinfold formulas versus air displacement plethysmography for estimating percent body fat in female adolescents with phenylketonuria. Jimd Reports. 10: 23-31. PMID 23430796 DOI: 10.1007/8904_2012_196  0.614
2010 Singh RH, Quirk ME, Douglas TD, Brauchla MC. BH(4) therapy impacts the nutrition status and intake in children with phenylketonuria: 2-year follow-up. Journal of Inherited Metabolic Disease. 33: 689-95. PMID 20941642 DOI: 10.1007/S10545-010-9224-1  0.668
2008 Douglas TD, Kennedy M, Singh RH. Comparison of 5 anthropometric skinfold formulas to air displacement plethysmography (ADP) when predicting body fat composition in female adolescents with phenylketonuria (PKU) The Faseb Journal. 22: 743-743. DOI: 10.1096/Fasebj.22.2_Supplement.743  0.597
Low-probability matches (unlikely to be authored by this person)
2019 Schoen M, Coakley K, Douglas T, Singh R. Functional Biomarkers of Vitamin B12 Status, Diet, and Metabolic Control in Women with Phenylketonuria (P24-005-19). Current Developments in Nutrition. 3. PMID 31223895 DOI: 10.1093/cdn/nzz044.P24-005-19  0.172
2006 Li RW, Theriault AG, Au K, Douglas TD, Casaschi A, Kurowska EM, Mukherjee R. Citrus polymethoxylated flavones improve lipid and glucose homeostasis and modulate adipocytokines in fructose-induced insulin resistant hamsters. Life Sciences. 79: 365-73. PMID 16497336 DOI: 10.1016/j.lfs.2006.01.023  0.116
2006 Li RW, Douglas TD, Maiyoh GK, Adeli K, Theriault AG. Green tea leaf extract improves lipid and glucose homeostasis in a fructose-fed insulin-resistant hamster model. Journal of Ethnopharmacology. 104: 24-31. PMID 16202550 DOI: 10.1016/J.Jep.2005.08.045  0.103
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