Derks TGJ - Search Results

1

A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers: from bedside to home site monitoring.

Hoogeveen IJ, Peeks F, de Boer F, Lubout CMA, de Koning TJ, Te Boekhorst S, Zandvoort RJ, Burghard R, van Spronsen FJ, Derks TGJ. Hoogeveen IJ, et al. Among authors: derks tgj. J Inherit Metab Dis. 2018 Nov;41(6):929-936. doi: 10.1007/s10545-018-0167-2. Epub 2018 Mar 29. J Inherit Metab Dis. 2018. PMID: 29600495 Free PMC article.

2

Safe and unsafe duration of fasting for children with MCAD deficiency.

Derks TG, van Spronsen FJ, Rake JP, van der Hilst CS, Span MM, Smit GP. Derks TG, et al. Eur J Pediatr. 2007 Jan;166(1):5-11. doi: 10.1007/s00431-006-0186-0. Epub 2006 Jun 21. Eur J Pediatr. 2007. PMID: 16788829

3

Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency.

Derks TG, Boer TS, van Assen A, Bos T, Ruiter J, Waterham HR, Niezen-Koning KE, Wanders RJ, Rondeel JM, Loeber JG, Ten Kate LP, Smit GP, Reijngoud DJ. Derks TG, et al. J Inherit Metab Dis. 2008 Feb;31(1):88-96. doi: 10.1007/s10545-007-0492-3. Epub 2008 Jan 14. J Inherit Metab Dis. 2008. PMID: 18188679

4

Dietary treatment of glycogen storage disease type Ia: uncooked cornstarch and/or continuous nocturnal gastric drip-feeding?

Derks TG, Martens DH, Sentner CP, van Rijn M, de Boer F, Smit GP, van Spronsen FJ. Derks TG, et al. Mol Genet Metab. 2013 May;109(1):1-2. doi: 10.1016/j.ymgme.2013.02.005. Epub 2013 Feb 15. Mol Genet Metab. 2013. PMID: 23480859 No abstract available.

5

Single amino acid supplementation in aminoacidopathies: a systematic review.

van Vliet D, Derks TG, van Rijn M, de Groot MJ, MacDonald A, Heiner-Fokkema MR, van Spronsen FJ. van Vliet D, et al. Orphanet J Rare Dis. 2014 Jan 13;9:7. doi: 10.1186/1750-1172-9-7. Orphanet J Rare Dis. 2014. PMID: 24422943 Free PMC article. Review.

6

Experimental evidence for protein oxidative damage and altered antioxidant defense in patients with medium-chain acyl-CoA dehydrogenase deficiency.

Derks TG, Touw CM, Ribas GS, Biancini GB, Vanzin CS, Negretto G, Mescka CP, Reijngoud DJ, Smit GP, Wajner M, Vargas CR. Derks TG, et al. J Inherit Metab Dis. 2014 Sep;37(5):783-9. doi: 10.1007/s10545-014-9700-0. Epub 2014 Mar 13. J Inherit Metab Dis. 2014. PMID: 24623196

7

Recombinant phenylalanine ammonia lyase in phenylketonuria.

van Spronsen FJ, Derks TG. van Spronsen FJ, et al. Lancet. 2014 Jul 5;384(9937):6-8. doi: 10.1016/S0140-6736(13)62075-9. Epub 2014 Apr 14. Lancet. 2014. PMID: 24742999 No abstract available.

8

Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children.

Brown LM, Corrado MM, van der Ende RM, Derks TG, Chen MA, Siegel S, Hoyt K, Correia CE, Lumpkin C, Flanagan TB, Carreras CT, Weinstein DA. Brown LM, et al. J Inherit Metab Dis. 2015 May;38(3):489-93. doi: 10.1007/s10545-014-9744-1. Epub 2014 Jul 29. J Inherit Metab Dis. 2015. PMID: 25070466

9

Dietary management in glycogen storage disease type III: what is the evidence?

Derks TG, Smit GP. Derks TG, et al. J Inherit Metab Dis. 2015 May;38(3):545-50. doi: 10.1007/s10545-014-9756-x. Epub 2014 Aug 28. J Inherit Metab Dis. 2015. PMID: 25164784 Review.

10

In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases.

Nalin T, Venema K, Weinstein DA, de Souza CF, Perry ID, van Wandelen MT, van Rijn M, Smit GP, Schwartz IV, Derks TG. Nalin T, et al. J Inherit Metab Dis. 2015 May;38(3):529-36. doi: 10.1007/s10545-014-9763-y. Epub 2014 Sep 16. J Inherit Metab Dis. 2015. PMID: 25224825

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