| 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 |
0.483 |
|
| 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 |
0.54 |
|
| 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 |
0.566 |
|
| 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 |
0.571 |
|
| 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 |
0.521 |
|
| 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 |
0.594 |
|
| 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 |
0.485 |
|
| 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 |
0.571 |
|
| 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 |
0.53 |
|
| 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 |
0.615 |
|
| 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 |
0.669 |
|
| 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 |
0.598 |
|
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