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Results: 9

1.

Improving cancer patient care: development of a generic cancer consumer quality index questionnaire for cancer patients.

Booij JC, Zegers M, Evers PM, Hendriks M, Delnoij DM, Rademakers JJ.

BMC Cancer. 2013 Apr 23;13:203. doi: 10.1186/1471-2407-13-203.

2.

Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.

Boon CJ, van den Born LI, Visser L, Keunen JE, Bergen AA, Booij JC, Riemslag FC, Florijn RJ, van Schooneveld MJ.

Ophthalmology. 2013 Apr;120(4):809-20. doi: 10.1016/j.ophtha.2012.09.057. Epub 2013 Jan 3.

PMID:
23290749
3.

Assessing quality of care in pediatric asthma: applicability of a revised version of the QUOTE-CNSLD questionnaire.

Kuethe MC, Sixma HJ, Vaessen-Verberne AA, Booij JC, van Aalderen WM.

J Asthma. 2012 Nov;49(9):966-76. doi: 10.3109/02770903.2012.721434. Epub 2012 Oct 1.

PMID:
23025477
4.

Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip.

Booij JC, Bakker A, Kulumbetova J, Moutaoukil Y, Smeets B, Verheij J, Kroes HY, Klaver CC, van Schooneveld M, Bergen AA, Florijn RJ.

Ophthalmology. 2011 Jan;118(1):160-167.e1-3. doi: 10.1016/j.ophtha.2010.04.022.

PMID:
20801516
5.

A new strategy to identify and annotate human RPE-specific gene expression.

Booij JC, ten Brink JB, Swagemakers SM, Verkerk AJ, Essing AH, van der Spek PJ, Bergen AA.

PLoS One. 2010 Mar 9;5(5):e9341. doi: 10.1371/journal.pone.0009341.

6.

Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.

Booij JC, Boon CJ, van Schooneveld MJ, ten Brink JB, Bakker A, de Jong PT, Hoyng CB, Bergen AA, Klaver CC.

Ophthalmology. 2010 Jul;117(7):1415-22. doi: 10.1016/j.ophtha.2009.11.044. Epub 2010 Apr 9.

PMID:
20381869
7.

The dynamic nature of Bruch's membrane.

Booij JC, Baas DC, Beisekeeva J, Gorgels TG, Bergen AA.

Prog Retin Eye Res. 2010 Jan;29(1):1-18. doi: 10.1016/j.preteyeres.2009.08.003. Epub 2009 Sep 10. Review.

PMID:
19747980
8.

Functional annotation of the human retinal pigment epithelium transcriptome.

Booij JC, van Soest S, Swagemakers SM, Essing AH, Verkerk AJ, van der Spek PJ, Gorgels TG, Bergen AA.

BMC Genomics. 2009 Apr 20;10:164. doi: 10.1186/1471-2164-10-164.

9.

Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.

Booij JC, Florijn RJ, ten Brink JB, Loves W, Meire F, van Schooneveld MJ, de Jong PT, Bergen AA.

J Med Genet. 2005 Nov;42(11):e67.

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