Santra S - Search Results

1

Dietary Management, Clinical Status and Outcome of Patients with Citrin Deficiency in the UK.

Pinto A, Ashmore C, Batzios S, Daly A, Dawson C, Dixon M, Evans S, Green D, Gribben J, Hunjan I, Jameson E, Newby C, Pierre G, Rajwal S, Robertson L, Santra S, Sharrard M, Vara R, White L, Wilcox G, Yilmaz O, MacDonald A. Pinto A, et al. Among authors: santra s. Nutrients. 2020 Oct 29;12(11):3313. doi: 10.3390/nu12113313. Nutrients. 2020. PMID: 33137944 Free PMC article.

2

The challenges of vitamin and mineral supplementation in children with inherited metabolic disorders: a prospective trial.

Daly A, Evans S, Chahal S, Surplice I, Vijay S, Santra S, MacDonald A. Daly A, et al. Among authors: santra s. J Hum Nutr Diet. 2016 Aug;29(4):434-40. doi: 10.1111/jhn.12354. Epub 2016 Jan 18. J Hum Nutr Diet. 2016. PMID: 26781762 Clinical Trial.

3

The challenge of nutritional profiling of a protein-free feed module for children on low protein tube feeds with organic acidaemias.

Daly A, Evans S, Ashmore C, Chahal S, Santra S, MacDonald A. Daly A, et al. Among authors: santra s. J Hum Nutr Diet. 2017 Jun;30(3):292-301. doi: 10.1111/jhn.12455. Epub 2017 Mar 10. J Hum Nutr Diet. 2017. PMID: 28294445

4

Refining low protein modular feeds for children on low protein tube feeds with organic acidaemias.

Daly A, Evans S, Ashmore C, Chahal S, Santra S, MacDonald A. Daly A, et al. Among authors: santra s. Mol Genet Metab Rep. 2017 Oct 7;13:99-104. doi: 10.1016/j.ymgmr.2017.08.003. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 29034175 Free PMC article.

5

The Nutritional Intake of Patients with Organic Acidaemias on Enteral Tube Feeding: Can We Do Better?

Daly A, Evans S, Gerrard A, Santra S, Vijay S, MacDonald A. Daly A, et al. Among authors: santra s. JIMD Rep. 2016;28:29-39. doi: 10.1007/8904_2015_443. Epub 2015 Oct 29. JIMD Rep. 2016. PMID: 26510853 Free PMC article.

6

Glycomacropeptide: long-term use and impact on blood phenylalanine, growth and nutritional status in children with PKU.

Daly A, Evans S, Chahal S, Santra S, Pinto A, Jackson R, Gingell C, Rocha J, Van Spronsen FJ, MacDonald A. Daly A, et al. Among authors: santra s. Orphanet J Rare Dis. 2019 Feb 15;14(1):44. doi: 10.1186/s13023-019-1011-y. Orphanet J Rare Dis. 2019. PMID: 30770754 Free PMC article. Review.

7

Glycomacropeptide in children with phenylketonuria: does its phenylalanine content affect blood phenylalanine control?

Daly A, Evans S, Chahal S, Santra S, MacDonald A. Daly A, et al. Among authors: santra s. J Hum Nutr Diet. 2017 Aug;30(4):515-523. doi: 10.1111/jhn.12438. Epub 2017 Jan 22. J Hum Nutr Diet. 2017. PMID: 28111827

8

Long-term outcome of isobutyryl-CoA dehydrogenase deficiency diagnosed following an episode of ketotic hypoglycaemia.

Santra S, Macdonald A, Preece MA, Olsen RK, Andresen BS. Santra S, et al. Mol Genet Metab Rep. 2016 Dec 22;10:28-30. doi: 10.1016/j.ymgmr.2016.11.005. eCollection 2017 Mar. Mol Genet Metab Rep. 2016. PMID: 28053874 Free PMC article.

9

Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England.

Broomfield A, Davison J, Roberts J, Stewart C, Hensman P, Beesley C, Tylee K, Rust S, Schwahn B, Jameson E, Vijay S, Santra S, Sreekantam S, Ramaswami U, Chakrapani A, Raiman J, Cleary MA, Jones SA. Broomfield A, et al. Among authors: santra s. Mol Genet Metab. 2020 Feb;129(2):98-105. doi: 10.1016/j.ymgme.2019.07.016. Epub 2019 Jul 30. Mol Genet Metab. 2020. PMID: 31383595

10

The challenges of managing coexistent disorders with phenylketonuria: 30 cases.

MacDonald A, Ahring K, Almeida MF, Belanger-Quintana A, Blau N, Burlina A, Cleary M, Coskum T, Dokoupil K, Evans S, Feillet F, Giżewska M, Gokmen Ozel H, Lotz-Havla AS, Kamieńska E, Maillot F, Lammardo AM, Muntau AC, Puchwein-Schwepcke A, Robert M, Rocha JC, Santra S, Skeath R, Strączek K, Trefz FK, van Dam E, van Rijn M, van Spronsen F, Vijay S. MacDonald A, et al. Among authors: santra s. Mol Genet Metab. 2015 Dec;116(4):242-51. doi: 10.1016/j.ymgme.2015.10.001. Epub 2015 Oct 9. Mol Genet Metab. 2015. PMID: 26498184

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