Derks TG - Search Results

1

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.

2

The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study.

Derks TG, Duran M, Waterham HR, Reijngoud DJ, Ten Kate LP, Smit GP. Derks TG, et al. Eur J Hum Genet. 2005 Aug;13(8):947-52. doi: 10.1038/sj.ejhg.5201428. Eur J Hum Genet. 2005. PMID: 15870827

3

The natural history of medium-chain acyl CoA dehydrogenase deficiency in the Netherlands: clinical presentation and outcome.

Derks TG, Reijngoud DJ, Waterham HR, Gerver WJ, van den Berg MP, Sauer PJ, Smit GP. Derks TG, et al. J Pediatr. 2006 May;148(5):665-670. doi: 10.1016/j.jpeds.2005.12.028. J Pediatr. 2006. PMID: 16737882

4

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

5

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. Among authors: derks tg. J Pediatr. 2007 Aug;151(2):115-20, 120.e1-3. doi: 10.1016/j.jpeds.2007.03.013. J Pediatr. 2007. PMID: 17643759

6

Inhibition of mitochondrial fatty acid oxidation in vivo only slightly suppresses gluconeogenesis but enhances clearance of glucose in mice.

Derks TG, van Dijk TH, Grefhorst A, Rake JP, Smit GP, Kuipers F, Reijngoud DJ. Derks TG, et al. Hepatology. 2008 Mar;47(3):1032-42. doi: 10.1002/hep.22101. Hepatology. 2008. PMID: 18302288

7

Disturbed hepatic carbohydrate management during high metabolic demand in medium-chain acyl-CoA dehydrogenase (MCAD)-deficient mice.

Herrema H, Derks TG, van Dijk TH, Bloks VW, Gerding A, Havinga R, Tietge UJ, Müller M, Smit GP, Kuipers F, Reijngoud DJ. Herrema H, et al. Among authors: derks tg. Hepatology. 2008 Jun;47(6):1894-904. doi: 10.1002/hep.22284. Hepatology. 2008. PMID: 18459129

8

Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study.

Touw CM, Smit GP, de Vries M, de Klerk JB, Bosch AM, Visser G, Mulder MF, Rubio-Gozalbo ME, Elvers B, Niezen-Koning KE, Wanders RJ, Waterham HR, Reijngoud DJ, Derks TG. Touw CM, et al. Among authors: derks tg. Orphanet J Rare Dis. 2012 May 25;7:30. doi: 10.1186/1750-1172-7-30. Orphanet J Rare Dis. 2012. PMID: 22630369 Free PMC article.

9

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.

10

In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.

Touw CM, Smit GP, Niezen-Koning KE, Bosgraaf-de Boer C, Gerding A, Reijngoud DJ, Derks TG. Touw CM, et al. Among authors: derks tg. Orphanet J Rare Dis. 2013 Mar 20;8:43. doi: 10.1186/1750-1172-8-43. Orphanet J Rare Dis. 2013. PMID: 23509891 Free PMC article.

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