Boon CJ - Search Results

1

Clinical and genetic characteristics of late-onset Stargardt's disease.

Westeneng-van Haaften SC, Boon CJ, Cremers FP, Hoefsloot LH, den Hollander AI, Hoyng CB. Westeneng-van Haaften SC, et al. Among authors: boon cj. Ophthalmology. 2012 Jun;119(6):1199-210. doi: 10.1016/j.ophtha.2012.01.005. Epub 2012 Mar 24. Ophthalmology. 2012. PMID: 22449572

2

Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants.

Mukhopadhyay A, Nikopoulos K, Maugeri A, de Brouwer AP, van Nouhuys CE, Boon CJ, Perveen R, Zegers HA, Wittebol-Post D, van den Biesen PR, van der Velde-Visser SD, Brunner HG, Black GC, Hoyng CB, Cremers FP. Mukhopadhyay A, et al. Among authors: boon cj. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3565-72. doi: 10.1167/iovs.06-0141. Invest Ophthalmol Vis Sci. 2006. PMID: 16877430

3

Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus.

Boon CJ, van Schooneveld MJ, den Hollander AI, van Lith-Verhoeven JJ, Zonneveld-Vrieling MN, Theelen T, Cremers FP, Hoyng CB, Klevering BJ. Boon CJ, et al. Br J Ophthalmol. 2007 Nov;91(11):1504-11. doi: 10.1136/bjo.2007.115659. Epub 2007 May 15. Br J Ophthalmol. 2007. PMID: 17504850 Free PMC article.

4

Clinical and genetic heterogeneity in multifocal vitelliform dystrophy.

Boon CJ, Klevering BJ, den Hollander AI, Zonneveld MN, Theelen T, Cremers FP, Hoyng CB. Boon CJ, et al. Arch Ophthalmol. 2007 Aug;125(8):1100-6. doi: 10.1001/archopht.125.8.1100. Arch Ophthalmol. 2007. PMID: 17698758

5

Analysis of visual pigment by fundus autofluorescence.

Theelen T, Berendschot TT, Boon CJ, Hoyng CB, Klevering BJ. Theelen T, et al. Among authors: boon cj. Exp Eye Res. 2008 Feb;86(2):296-304. doi: 10.1016/j.exer.2007.10.022. Epub 2007 Nov 12. Exp Eye Res. 2008. PMID: 18096158

6

Basal laminar drusen caused by compound heterozygous variants in the CFH gene.

Boon CJ, Klevering BJ, Hoyng CB, Zonneveld-Vrieling MN, Nabuurs SB, Blokland E, Cremers FP, den Hollander AI. Boon CJ, et al. Am J Hum Genet. 2008 Feb;82(2):516-23. doi: 10.1016/j.ajhg.2007.11.007. Am J Hum Genet. 2008. PMID: 18252232 Free PMC article.

7

Fundus autofluorescence imaging of retinal dystrophies.

Boon CJ, Jeroen Klevering B, Keunen JE, Hoyng CB, Theelen T. Boon CJ, et al. Vision Res. 2008 Nov;48(26):2569-77. doi: 10.1016/j.visres.2008.01.010. Epub 2008 Mar 4. Vision Res. 2008. PMID: 18289629

8

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene.

Boon CJ, den Hollander AI, Hoyng CB, Cremers FP, Klevering BJ, Keunen JE. Boon CJ, et al. Prog Retin Eye Res. 2008 Mar;27(2):213-35. doi: 10.1016/j.preteyeres.2008.01.002. Epub 2008 Jan 26. Prog Retin Eye Res. 2008. PMID: 18328765 Review.

9

[Fundus autofluorescence in patients with inherited retinal diseases : patterns of fluorescence at two different wavelengths].

Theelen T, Boon CJ, Klevering BJ, Hoyng CB. Theelen T, et al. Among authors: boon cj. Ophthalmologe. 2008 Nov;105(11):1013-22. doi: 10.1007/s00347-008-1695-1. Ophthalmologe. 2008. PMID: 18415102 German.

10

Central areolar choroidal dystrophy.

Boon CJ, Klevering BJ, Cremers FP, Zonneveld-Vrieling MN, Theelen T, Den Hollander AI, Hoyng CB. Boon CJ, et al. Ophthalmology. 2009 Apr;116(4):771-82, 782.e1. doi: 10.1016/j.ophtha.2008.12.019. Epub 2009 Feb 25. Ophthalmology. 2009. PMID: 19243827

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