Derks TGJ - Search Results

1

Abnormal glucose homeostasis and fasting intolerance in patients with congenital porto-systemic shunts.

van Albada ME, Shah P, Derks TGJ, Fuchs S, Jans JJM, McLin V, van der Doef HPJ. van Albada ME, et al. Among authors: derks tgj. Front Endocrinol (Lausanne). 2023 Aug 18;14:1190473. doi: 10.3389/fendo.2023.1190473. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37664849 Free PMC article. Review.

2

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

3

Erratum to: 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 Sep;38(5):987. doi: 10.1007/s10545-015-9858-0. J Inherit Metab Dis. 2015. PMID: 25989743 Free article. No abstract available.

4

[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.

5

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.

6

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

7

Determination of amylose/amylopectin ratio of starches.

Nalin T, Sperb-Ludwig F, Venema K, Derks TG, Schwartz IV. Nalin T, et al. J Inherit Metab Dis. 2015 Sep;38(5):985-6. doi: 10.1007/s10545-015-9850-8. Epub 2015 Apr 29. J Inherit Metab Dis. 2015. PMID: 25921820 No abstract available.

8

Clinical pathways for inborn errors of metabolism: warranted and feasible.

Demirdas S, van Kessel IN, Korndewal MJ, Hollak CE, Meutgeert H, Klaren A, van Rijn M, van Spronsen FJ, Bosch AM; Dutch working Group. Demirdas S, et al. Orphanet J Rare Dis. 2013 Feb 25;8:37. doi: 10.1186/1750-1172-8-37. Orphanet J Rare Dis. 2013. PMID: 23442887 Free PMC article.

9

Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study.

Global PaedSurg Research Collaboration. Global PaedSurg Research Collaboration. Lancet. 2021 Jul 24;398(10297):325-339. doi: 10.1016/S0140-6736(21)00767-4. Epub 2021 Jul 13. Lancet. 2021. PMID: 34270932 Free PMC article.

10

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

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