Douglas TD - Search Results

1

One-year follow-up of B vitamin and Iron status in patients with phenylketonuria provided tetrahydrobiopterin (BH4).

Brantley KD, Douglas TD, Singh RH. Brantley KD, et al. Among authors: douglas td. Orphanet J Rare Dis. 2018 Oct 30;13(1):192. doi: 10.1186/s13023-018-0923-2. Orphanet J Rare Dis. 2018. PMID: 30373601 Free PMC article. Clinical Trial.

2

BH(4) therapy impacts the nutrition status and intake in children with phenylketonuria: 2-year follow-up.

Singh RH, Quirk ME, Douglas TD, Brauchla MC. Singh RH, et al. Among authors: douglas td. J Inherit Metab Dis. 2010 Dec;33(6):689-95. doi: 10.1007/s10545-010-9224-1. Epub 2010 Oct 13. J Inherit Metab Dis. 2010. PMID: 20941642 Clinical Trial.

3

The effects of sapropterin on urinary monoamine metabolites in phenylketonuria.

Douglas TD, Jinnah HA, Bernhard D, Singh RH. Douglas TD, et al. Mol Genet Metab. 2013 Jul;109(3):243-50. doi: 10.1016/j.ymgme.2013.04.017. Epub 2013 May 1. Mol Genet Metab. 2013. PMID: 23712020

4

Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride.

Douglas TD, Ramakrishnan U, Kable JA, Singh RH. Douglas TD, et al. Health Qual Life Outcomes. 2013 Dec 30;11:218. doi: 10.1186/1477-7525-11-218. Health Qual Life Outcomes. 2013. PMID: 24373161 Free PMC article.

5

Protein intake and physical activity are associated with body composition in individuals with phenylalanine hydroxylase deficiency.

Jani R, Coakley K, Douglas T, Singh R. Jani R, et al. Mol Genet Metab. 2017 Jun;121(2):104-110. doi: 10.1016/j.ymgme.2017.04.012. Epub 2017 Apr 28. Mol Genet Metab. 2017. PMID: 28465125

6

Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency.

Coakley KE, Douglas TD, Goodman M, Ramakrishnan U, Dobrowolski SF, Singh RH. Coakley KE, et al. Among authors: douglas td. J Inherit Metab Dis. 2016 May;39(3):363-372. doi: 10.1007/s10545-015-9910-0. Epub 2016 Feb 16. J Inherit Metab Dis. 2016. PMID: 26883219

7

Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach.

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, Rohr F. Singh RH, et al. Among authors: douglas td. Mol Genet Metab. 2016 Jun;118(2):72-83. doi: 10.1016/j.ymgme.2016.04.008. Epub 2016 Apr 17. Mol Genet Metab. 2016. PMID: 27211276 Review.

8

Large neutral amino acid status in association with P:T ratio and diet in adult and pediatric patients with phenylketonuria.

Douglas TD, Nucci AM, Berry AM, Henes ST, Singh RH. Douglas TD, et al. JIMD Rep. 2019 Sep 16;50(1):50-59. doi: 10.1002/jmd2.12076. eCollection 2019 Nov. JIMD Rep. 2019. PMID: 31741827 Free PMC article.

9

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).

Douglas TD, Newby LK, Eckstrand J, Wixted D, Singh RH. Douglas TD, et al. Mol Genet Metab Rep. 2020 Oct 14;25:100651. doi: 10.1016/j.ymgmr.2020.100651. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33088714 Free PMC article.

10

Accuracy of six anthropometric skinfold formulas versus air displacement plethysmography for estimating percent body fat in female adolescents with phenylketonuria.

Douglas TD, Kennedy MJ, Quirk ME, Yi SH, Singh RH. Douglas TD, et al. JIMD Rep. 2013;10:23-31. doi: 10.1007/8904_2012_196. Epub 2012 Dec 29. JIMD Rep. 2013. PMID: 23430796 Free PMC article.

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