Hollak CE - Search Results

1

High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trial.

ten Hoedt AE, de Sonneville LM, Francois B, ter Horst NM, Janssen MC, Rubio-Gozalbo ME, Wijburg FA, Hollak CE, Bosch AM. ten Hoedt AE, et al. Among authors: hollak ce. J Inherit Metab Dis. 2011 Feb;34(1):165-71. doi: 10.1007/s10545-010-9253-9. Epub 2010 Dec 10. J Inherit Metab Dis. 2011. PMID: 21153445 Free PMC article. Clinical Trial.

2

The effect of enzyme therapy in a patient with Gaucher disease type III.

Bosman DK, Hollak CE, Aerts JM, Bakker HD. Bosman DK, et al. Among authors: hollak ce. J Inherit Metab Dis. 1996;19(5):703-4. doi: 10.1007/BF01799852. J Inherit Metab Dis. 1996. PMID: 8892032 No abstract available.

3

The natural course of Gaucher disease in The Netherlands: implications for monitoring of disease manifestations.

Maaswinkel-Mooij P, Hollak C, van Eysden-Plaisier M, Prins M, Aerts H, Pöll R. Maaswinkel-Mooij P, et al. J Inherit Metab Dis. 2000 Feb;23(1):77-82. doi: 10.1023/a:1005655031239. J Inherit Metab Dis. 2000. PMID: 10682310

4

Clinically relevant therapeutic endpoints in type I Gaucher disease.

Hollak CE, Maas M, Aerts JM. Hollak CE, et al. J Inherit Metab Dis. 2001;24 Suppl 2:97-105; discussion 87-8. doi: 10.1023/a:1012492429191. J Inherit Metab Dis. 2001. PMID: 11758685 Review.

5

Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick disease.

Brinkman J, Wijburg FA, Hollak CE, Groener JE, Verhoek M, Scheij S, Aten J, Boot RG, Aerts JM. Brinkman J, et al. Among authors: hollak ce. J Inherit Metab Dis. 2005;28(1):13-20. doi: 10.1007/s10545-005-4416-9. J Inherit Metab Dis. 2005. PMID: 15702402

6

Manifestations of Fabry disease in placental tissue.

Vedder AC, Strijland A, vd Bergh Weerman MA, Florquin S, Aerts JM, Hollak CE. Vedder AC, et al. Among authors: hollak ce. J Inherit Metab Dis. 2006 Feb;29(1):106-11. doi: 10.1007/s10545-006-0196-0. J Inherit Metab Dis. 2006. PMID: 16601876

7

CCL18: a urinary marker of Gaucher cell burden in Gaucher patients.

Boot RG, Verhoek M, Langeveld M, Renkema GH, Hollak CE, Weening JJ, Donker-Koopman WE, Groener JE, Aerts JM. Boot RG, et al. Among authors: hollak ce. J Inherit Metab Dis. 2006 Aug;29(4):564-71. doi: 10.1007/s10545-006-0318-8. Epub 2006 May 30. J Inherit Metab Dis. 2006. PMID: 16736095

8

Substrate reduction therapy of glycosphingolipid storage disorders.

Aerts JM, Hollak CE, Boot RG, Groener JE, Maas M. Aerts JM, et al. Among authors: hollak ce. J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):449-56. doi: 10.1007/s10545-006-0272-5. J Inherit Metab Dis. 2006. PMID: 16763917

9

Restricted upper extremity range of motion in mucopolysaccharidosis type I: no response to one year of enzyme replacement therapy.

Cox-Brinkman J, Smeulders MJ, Hollak CE, Wijburg FA. Cox-Brinkman J, et al. Among authors: hollak ce. J Inherit Metab Dis. 2007 Feb;30(1):47-50. doi: 10.1007/s10545-006-0490-x. Epub 2006 Dec 11. J Inherit Metab Dis. 2007. PMID: 17160613

10

The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels.

Vedder AC, Linthorst GE, van Breemen MJ, Groener JE, Bemelman FJ, Strijland A, Mannens MM, Aerts JM, Hollak CE. Vedder AC, et al. Among authors: hollak ce. J Inherit Metab Dis. 2007 Feb;30(1):68-78. doi: 10.1007/s10545-006-0484-8. Epub 2007 Jan 5. J Inherit Metab Dis. 2007. PMID: 17206462

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