Derks TGJ - Search Results

1

Repurposing empagliflozin in individuals with glycogen storage disease Ib: A value-based healthcare approach and systematic benefit-risk assessment.

Derks TGJ, Venema A, Köller C, Bos E, Overduin RJ, Stolwijk NN, Hofbauer P, Bolhuis MS, van Eenennaam F, Groen H, Hollak CEM, Wortmann SB. Derks TGJ, et al. J Inherit Metab Dis. 2024 Mar;47(2):244-254. doi: 10.1002/jimd.12714. Epub 2024 Jan 7. J Inherit Metab Dis. 2024. PMID: 38185897

2

[Deficiency of the fatty-acid oxidising enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in an adult, detected during a neonatal screening programme].

Derks TG, Jakobs H, Gerding A, Niezen-Koning KE, Reijngoud DJ, Smit GP. Derks TG, et al. Ned Tijdschr Geneeskd. 2004 Oct 30;148(44):2185-90. Ned Tijdschr Geneeskd. 2004. PMID: 15559414 Dutch.

3

Acute hepatic steatosis in mice by blocking beta-oxidation does not reduce insulin sensitivity of very-low-density lipoprotein production.

Grefhorst A, Hoekstra J, Derks TG, Ouwens DM, Baller JF, Havinga R, Havekes LM, Romijn JA, Kuipers F. Grefhorst A, et al. Am J Physiol Gastrointest Liver Physiol. 2005 Sep;289(3):G592-8. doi: 10.1152/ajpgi.00063.2005. Epub 2005 Apr 7. Am J Physiol Gastrointest Liver Physiol. 2005. PMID: 15817811 Free article.

4

Cost-effectiveness of neonatal screening for medium chain acyl-CoA dehydrogenase deficiency: the homogeneous population of The Netherlands.

van der Hilst CS, Derks TG, Reijngoud DJ, Smit GP, TenVergert EM. van der Hilst CS, et al. J Pediatr. 2007 Aug;151(2):115-20, 120.e1-3. doi: 10.1016/j.jpeds.2007.03.013. J Pediatr. 2007. PMID: 17643759

5

Analysis of body composition and nutritional status in Brazilian phenylketonuria patients.

Mazzola PN, Nalin T, Castro K, van Rijn M, Derks TG, Perry ID, Mainieri AS, Schwartz IV. Mazzola PN, et al. Mol Genet Metab Rep. 2016 Jan 9;6:16-20. doi: 10.1016/j.ymgmr.2015.12.003. eCollection 2016 Mar. Mol Genet Metab Rep. 2016. PMID: 27014574 Free PMC article.

6

MPV17: fatal hepatocerebral presentation in a Brazilian infant.

Nogueira C, de Souza CF, Husny A, Derks TG, Santorelli FM, Vilarinho L. Nogueira C, et al. Mol Genet Metab. 2012 Dec;107(4):764. doi: 10.1016/j.ymgme.2012.10.010. Epub 2012 Oct 23. Mol Genet Metab. 2012. PMID: 23137571 No abstract available.

7

Mutations in RARS cause hypomyelination.

Wolf NI, Salomons GS, Rodenburg RJ, Pouwels PJ, Schieving JH, Derks TG, Fock JM, Rump P, van Beek DM, van der Knaap MS, Waisfisz Q. Wolf NI, et al. Ann Neurol. 2014 Jul;76(1):134-9. doi: 10.1002/ana.24167. Epub 2014 May 16. Ann Neurol. 2014. PMID: 24777941

8

Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD⁺ in medium-chain acyl-CoA dehydrogenase knockout mice.

Martines AMF, Gerding A, Stolle S, Vieira-Lara MA, Wolters JC, Jurdzinski A, Bongiovanni L, de Bruin A, van der Vlies P, van der Vries G, Bloks VW, Derks TGJ, Reijngoud DJ, Bakker BM. Martines AMF, et al. Among authors: derks tgj. Sci Rep. 2019 Oct 10;9(1):14539. doi: 10.1038/s41598-019-50758-0. Sci Rep. 2019. PMID: 31601874 Free PMC article.

9

Acute exercise in treated phenylketonuria patients: Physical activity and biochemical response.

Mazzola PN, Teixeira BC, Schirmbeck GH, Reischak-Oliveira A, Derks TGJ, van Spronsen FJ, Dutra-Filho CS, Schwartz IVD. Mazzola PN, et al. Among authors: derks tgj. Mol Genet Metab Rep. 2015 Oct 22;5:55-59. doi: 10.1016/j.ymgmr.2015.10.003. eCollection 2015 Dec. Mol Genet Metab Rep. 2015. PMID: 28649544 Free PMC article.

10

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.

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