Gootjes J - Search Results

1

Laboratory evaluation of a novel capillary blood sampling device for measuring eight clinical chemistry parameters and HbA1c.

Gootjes J, Tel RM, Bergkamp FJ, Gorgels JP. Gootjes J, et al. Clin Chim Acta. 2009 Mar;401(1-2):152-7. doi: 10.1016/j.cca.2008.12.016. Epub 2008 Dec 24. Clin Chim Acta. 2009. PMID: 19138681

2

Jejunal Casein Feeding Is Followed by More Rapid Protein Digestion and Amino Acid Absorption When Compared with Gastric Feeding in Healthy Young Men.

Luttikhold J, van Norren K, Buijs N, Ankersmit M, Heijboer AC, Gootjes J, Rijna H, van Leeuwen PA, van Loon LJ. Luttikhold J, et al. Among authors: gootjes j. J Nutr. 2015 Sep;145(9):2033-8. doi: 10.3945/jn.115.211615. Epub 2015 Jul 29. J Nutr. 2015. PMID: 26224751 Free article. Clinical Trial.

3

Jejunal feeding is followed by a greater rise in plasma cholecystokinin, peptide YY, glucagon-like peptide 1, and glucagon-like peptide 2 concentrations compared with gastric feeding in vivo in humans: a randomized trial.

Luttikhold J, van Norren K, Rijna H, Buijs N, Ankersmit M, Heijboer AC, Gootjes J, Hartmann B, Holst JJ, van Loon LJ, van Leeuwen PA. Luttikhold J, et al. Among authors: gootjes j. Am J Clin Nutr. 2016 Feb;103(2):435-43. doi: 10.3945/ajcn.115.116251. Epub 2016 Jan 13. Am J Clin Nutr. 2016. PMID: 26762368 Free article. Clinical Trial.

4

Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism.

Gootjes J, Schmohl F, Mooijer PA, Dekker C, Mandel H, Topcu M, Huemer M, Von Schütz M, Marquardt T, Smeitink JA, Waterham HR, Wanders RJ. Gootjes J, et al. Hum Mutat. 2004 Aug;24(2):130-9. doi: 10.1002/humu.20062. Hum Mutat. 2004. PMID: 15241794

5

Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder.

Gootjes J, Schmohl F, Waterham HR, Wanders RJ. Gootjes J, et al. Eur J Hum Genet. 2004 Feb;12(2):115-20. doi: 10.1038/sj.ejhg.5201090. Eur J Hum Genet. 2004. PMID: 14571262

6

Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.

Gootjes J, Elpeleg O, Eyskens F, Mandel H, Mitanchez D, Shimozawa N, Suzuki Y, Waterham HR, Wanders RJ. Gootjes J, et al. Pediatr Res. 2004 Mar;55(3):431-6. doi: 10.1203/01.PDR.0000106862.83469.8D. Epub 2003 Nov 19. Pediatr Res. 2004. PMID: 14630978

7

Resolution of the molecular defect in a patient with peroxisomal mosaicism in the liver.

Gootjes J, Mandel H, Mooijer PA, Roels F, Waterham HR, Wanders RJ. Gootjes J, et al. Adv Exp Med Biol. 2003;544:107-11. doi: 10.1007/978-1-4419-9072-3_15. Adv Exp Med Biol. 2003. PMID: 14713221 No abstract available.

8

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.

Raas-Rothschild A, Wanders RJ, Mooijer PA, Gootjes J, Waterham HR, Gutman A, Suzuki Y, Shimozawa N, Kondo N, Eshel G, Espeel M, Roels F, Korman SH. Raas-Rothschild A, et al. Among authors: gootjes j. Am J Hum Genet. 2002 Apr;70(4):1062-8. doi: 10.1086/339766. Epub 2002 Feb 28. Am J Hum Genet. 2002. PMID: 11873320 Free PMC article.

9

Biochemical markers predicting survival in peroxisome biogenesis disorders.

Gootjes J, Mooijer PA, Dekker C, Barth PG, Poll-The BT, Waterham HR, Wanders RJ. Gootjes J, et al. Adv Exp Med Biol. 2003;544:67-8. doi: 10.1007/978-1-4419-9072-3_8. Adv Exp Med Biol. 2003. PMID: 14713214 No abstract available.

10

Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients.

Poll-The BT, Gootjes J, Duran M, De Klerk JB, Wenniger-Prick LJ, Admiraal RJ, Waterham HR, Wanders RJ, Barth PG. Poll-The BT, et al. Among authors: gootjes j. Am J Med Genet A. 2004 May 1;126A(4):333-8. doi: 10.1002/ajmg.a.20664. Am J Med Genet A. 2004. PMID: 15098231

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