Preece MA - Search Results

1

Wilson's Disease and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome in a Child: A Case Report with Lessons Learned!

Fernando M, Vijay S, Santra S, Preece MA, Brown R, Rodrigues A, Gupte GL. Fernando M, et al. Among authors: preece ma. Euroasian J Hepatogastroenterol. 2021 Jul-Dec;11(2):100-102. doi: 10.5005/jp-journals-10018-1351. Euroasian J Hepatogastroenterol. 2021. PMID: 34786365 Free PMC article.

2

The micronutrient status of patients with phenylketonuria on dietary treatment: an ongoing challenge.

Evans S, Daly A, MacDonald J, Preece MA, Santra S, Vijay S, Chakrapani A, MacDonald A. Evans S, et al. Among authors: preece ma. Ann Nutr Metab. 2014;65(1):42-8. doi: 10.1159/000363391. Epub 2014 Sep 4. Ann Nutr Metab. 2014. PMID: 25196394

3

The safety of Lipistart, a medium-chain triglyceride based formula, in the dietary treatment of long-chain fatty acid disorders: a phase I study.

MacDonald A, Webster R, Whitlock M, Gerrard A, Daly A, Preece MA, Evans S, Ashmore C, Chakrapani A, Vijay S, Santra S. MacDonald A, et al. Among authors: preece ma. J Pediatr Endocrinol Metab. 2018 Mar 28;31(3):297-304. doi: 10.1515/jpem-2017-0426. J Pediatr Endocrinol Metab. 2018. PMID: 29425111 Clinical Trial.

4

How to use a controlled fast to investigate hypoglycaemia.

Sreekantam S, Preece MA, Vijay S, Raiman J, Santra S. Sreekantam S, et al. Among authors: preece ma. Arch Dis Child Educ Pract Ed. 2017 Feb;102(1):28-36. doi: 10.1136/archdischild-2015-308702. Epub 2016 Aug 24. Arch Dis Child Educ Pract Ed. 2017. PMID: 27557839 Review.

5

Natural Protein Tolerance and Metabolic Control in Patients with Hereditary Tyrosinaemia Type 1.

Yilmaz O, Daly A, Pinto A, Ashmore C, Evans S, Gupte G, Santra S, Preece MA, Mckiernan P, Kitchen S, Ayhan NY, MacDonald A. Yilmaz O, et al. Among authors: preece ma. Nutrients. 2020 Apr 19;12(4):1148. doi: 10.3390/nu12041148. Nutrients. 2020. PMID: 32325917 Free PMC article.

6

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. Among authors: preece ma. 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.

7

Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis.

Santra S, Cameron JM, Shyr C, Zhang L, Drögemöller B, Ross CJ, Wasserman WW, Wevers RA, Rodenburg RJ, Gupte G, Preece MA, van Karnebeek CD. Santra S, et al. Among authors: preece ma. Mol Genet Metab. 2016 May;118(1):21-7. doi: 10.1016/j.ymgme.2016.03.001. Epub 2016 Mar 4. Mol Genet Metab. 2016. PMID: 26971250

8

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Rodrigues AF, Gray RG, Preece MA, Brown R, Hill FG, Baumann U, McKiernan PJ. Rodrigues AF, et al. Among authors: preece ma. Arch Dis Child. 2006 Oct;91(10):841-4. doi: 10.1136/adc.2005.088013. Epub 2006 May 31. Arch Dis Child. 2006. PMID: 16737996 Free PMC article.

9

Renal tubular function in children with tyrosinaemia type I treated with nitisinone.

Santra S, Preece MA, Hulton SA, McKiernan PJ. Santra S, et al. Among authors: preece ma. J Inherit Metab Dis. 2008 Jun;31(3):399-402. doi: 10.1007/s10545-008-0817-x. Epub 2008 May 23. J Inherit Metab Dis. 2008. PMID: 18509744

10

Dietary practices in glutaric aciduria type 1 over 16 years.

Gokmen-Ozel H, MacDonald A, Daly A, Ashmore C, Preece MA, Hendriksz C, Vijay S, Chakrapani A. Gokmen-Ozel H, et al. Among authors: preece ma. J Hum Nutr Diet. 2012 Dec;25(6):514-9. doi: 10.1111/j.1365-277X.2012.01269.x. Epub 2012 Jul 30. J Hum Nutr Diet. 2012. PMID: 22845646

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