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    Results: 1 to 50 of 88

    1.

    Near-infrared reflectance imaging of neovascular age-related macular degeneration.

    Theelen T, Berendschot TT, Hoyng CB, Boon CJ, Klevering BJ.

    Graefes Arch Clin Exp Ophthalmol. 2009 Dec;247(12):1625-33. Epub 2009 Jul 30.PMID: 19641931 [PubMed - in process]Related articlesFree article

    2.

    Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

    Thiadens AA, den Hollander AI, Roosing S, Nabuurs SB, Zekveld-Vroon RC, Collin RW, De Baere E, Koenekoop RK, van Schooneveld MJ, Strom TM, van Lith-Verhoeven JJ, Lotery AJ, van Moll-Ramirez N, Leroy BP, van den Born LI, Hoyng CB, Cremers FP, Klaver CC.

    Am J Hum Genet. 2009 Aug;85(2):240-7. Epub 2009 Jul 16.PMID: 19615668 [PubMed - indexed for MEDLINE]Related articles

    3.

    Genetic etiology and clinical consequences of complete and incomplete achromatopsia.

    Thiadens AA, Slingerland NW, Roosing S, van Schooneveld MJ, van Lith-Verhoeven JJ, van Moll-Ramirez N, van den Born LI, Hoyng CB, Cremers FP, Klaver CC.

    Ophthalmology. 2009 Oct;116(10):1984-9.e1. Epub 2009 Jul 9.PMID: 19592100 [PubMed - indexed for MEDLINE]Related articles

    4.

    Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.

    Boon CJ, Theelen T, Hoyng CB.

    Am J Ophthalmol. 2009 Jul;148(1):173-4; author reply 174-5. No abstract available. PMID: 19540988 [PubMed - indexed for MEDLINE]Related articles

    5.

    The spectrum of ocular phenotypes caused by mutations in the BEST1 gene.

    Boon CJ, Klevering BJ, Leroy BP, Hoyng CB, Keunen JE, den Hollander AI.

    Prog Retin Eye Res. 2009 May;28(3):187-205. Epub 2009 Apr 16. Review.PMID: 19375515 [PubMed - indexed for MEDLINE]Related articles

    6.

    Clinical and molecular genetic analysis of best vitelliform macular dystrophy.

    Boon CJ, Theelen T, Hoefsloot EH, van Schooneveld MJ, Keunen JE, Cremers FP, Klevering BJ, Hoyng CB.

    Retina. 2009 Jun;29(6):835-47.PMID: 19357557 [PubMed - indexed for MEDLINE]Related articles

    7.

    The spectrum of phenotypes caused by variants in the CFH gene.

    Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI.

    Mol Immunol. 2009 May;46(8-9):1573-94. Epub 2009 Mar 17. Review.PMID: 19297022 [PubMed - indexed for MEDLINE]Related articles

    8.

    Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.

    Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RW, Hoyng CB, Lopez I, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK, Chen R.

    Am J Hum Genet. 2009 Mar;84(3):380-7. Epub 2009 Mar 5.PMID: 19268277 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Central areolar choroidal dystrophy.

    Boon CJ, Klevering BJ, Cremers FP, Zonneveld-Vrieling MN, Theelen T, Den Hollander AI, Hoyng CB.

    Ophthalmology. 2009 Apr;116(4):771-82, 782.e1. Epub 2009 Feb 25.PMID: 19243827 [PubMed - indexed for MEDLINE]Related articles

    10.

    A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.

    Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI.

    Invest Ophthalmol Vis Sci. 2009 May;50(5):2344-50. Epub 2008 Dec 13.PMID: 19074807 [PubMed - indexed for MEDLINE]Related articles

    11.

    Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa.

    Collin RW, Littink KW, Klevering BJ, van den Born LI, Koenekoop RK, Zonneveld MN, Blokland EA, Strom TM, Hoyng CB, den Hollander AI, Cremers FP.

    Am J Hum Genet. 2008 Nov;83(5):594-603. Epub 2008 Oct 30.PMID: 18976725 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Intravenous diclofenac as prophylactic treatment for verteporfin-associated low back pain.

    Theelen T, Hoyng CB.

    Eur J Ophthalmol. 2008 Sep-Oct;18(5):805-8.PMID: 18850562 [PubMed - indexed for MEDLINE]Related articles

    13.

    Reflux after intravitreal injection of bevacizumab.

    Boon CJ, Crama N, Klevering BJ, van Kuijk FJ, Hoyng CB.

    Ophthalmology. 2008 Jul;115(7):1270; author reply 1271. No abstract available. PMID: 18598829 [PubMed - indexed for MEDLINE]Related articles

    14.

    Intravitreal triamcinolone for the treatment of refractory macular edema in idiopathic intermediate or posterior uveitis.

    Hogewind BF, Zijlstra C, Klevering BJ, Hoyng CB.

    Eur J Ophthalmol. 2008 May-Jun;18(3):429-34.PMID: 18465727 [PubMed - indexed for MEDLINE]Related articles

    15.

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

    Theelen T, Boon CJ, Klevering BJ, Hoyng CB.

    Ophthalmologe. 2008 Nov;105(11):1013-22. German. PMID: 18415102 [PubMed - indexed for MEDLINE]Related articles

    16.

    Novel human pathological mutations. Gene symbol: MYOC. Disease: primary open angle glaucoma.

    Mukhopadhyay A, Hogewind BF, Theelen T, Cremers FP, Hoyng CB.

    Hum Genet. 2007 Dec;122(5):553. No abstract available. PMID: 18383598 [PubMed - indexed for MEDLINE]Related articles

    17.

    Hypopigmentary fundus changes with cutaneous vitiligo.

    Vingerling JR, Owens S, van der Meijden WI, Hoyng CB, Bird AC.

    Arch Ophthalmol. 2008 Mar;126(3):439. No abstract available. PMID: 18332336 [PubMed - indexed for MEDLINE]Related articles

    18.

    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.

    Prog Retin Eye Res. 2008 Mar;27(2):213-35. Epub 2008 Jan 26. Review.PMID: 18328765 [PubMed - indexed for MEDLINE]Related articles

    19.

    Fundus autofluorescence imaging of retinal dystrophies.

    Boon CJ, Jeroen Klevering B, Keunen JE, Hoyng CB, Theelen T.

    Vision Res. 2008 Nov;48(26):2569-77. Epub 2008 Mar 4.PMID: 18289629 [PubMed - indexed for MEDLINE]Related articles

    20.

    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.

    Am J Hum Genet. 2008 Feb;82(2):516-23.PMID: 18252232 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Octreotide acetate in dominant cystoid macular dystrophy.

    Hogewind BF, Pieters G, Hoyng CB.

    Eur J Ophthalmol. 2008 Jan-Feb;18(1):99-103.PMID: 18203093 [PubMed - indexed for MEDLINE]Related articles

    22.

    Analysis of visual pigment by fundus autofluorescence.

    Theelen T, Berendschot TT, Boon CJ, Hoyng CB, Klevering BJ.

    Exp Eye Res. 2008 Feb;86(2):296-304. Epub 2007 Nov 12.PMID: 18096158 [PubMed - indexed for MEDLINE]Related articles

    23.

    [The Dutch version of the Radner Reading Chart for assessing vision function]

    Maaijwee KJ, Meulendijks CF, Radner W, van Meurs JC, Hoyng CB.

    Ned Tijdschr Geneeskd. 2007 Nov 10;151(45):2494-7. Review. Dutch. PMID: 18062591 [PubMed - indexed for MEDLINE]Related articles

    24.

    Identification and functional characterization of a novel MYOC mutation in two primary open angle glaucoma families from The Netherlands.

    Hogewind BF, Gaplovska-Kysela K, Theelen T, Cremers FP, Yam GH, Hoyng CB, Mukhopadhyay A.

    Mol Vis. 2007 Sep 27;13:1793-801.PMID: 17960117 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Clinical and genetic heterogeneity in multifocal vitelliform dystrophy.

    Boon CJ, Klevering BJ, den Hollander AI, Zonneveld MN, Theelen T, Cremers FP, Hoyng CB.

    Arch Ophthalmol. 2007 Aug;125(8):1100-6.PMID: 17698758 [PubMed - indexed for MEDLINE]Related articlesFree article

    26.

    Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosa.

    den Hollander AI, van Lith-Verhoeven JJ, Arends ML, Strom TM, Cremers FP, Hoyng CB.

    Arch Ophthalmol. 2007 Jul;125(7):932-5.PMID: 17620573 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    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.

    Br J Ophthalmol. 2007 Nov;91(11):1504-11. Epub 2007 May 15.PMID: 17504850 [PubMed - indexed for MEDLINE]Related articles

    28.

    Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.

    den Hollander AI, Koenekoop RK, Yzer S, Lopez I, Arends ML, Voesenek KE, Zonneveld MN, Strom TM, Meitinger T, Brunner HG, Hoyng CB, van den Born LI, Rohrschneider K, Cremers FP.

    Am J Hum Genet. 2006 Sep;79(3):556-61. Epub 2006 Jul 11.PMID: 16909394 [PubMed - indexed for MEDLINE]Related articlesFree article

    29.

    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.

    Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3565-72.PMID: 16877430 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    Long-term evaluation of eccentric viewing spectacles in patients with bilateral central scotomas.

    Verezen CA, Meulendijks CF, Hoyng CB, Klevering BJ.

    Optom Vis Sci. 2006 Feb;83(2):88-95.PMID: 16501410 [PubMed - indexed for MEDLINE]Related articles

    31.

    Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.

    Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4328-35.PMID: 16249515 [PubMed - indexed for MEDLINE]Related articlesFree article

    32.

    Genetic risk of rhegmatogenous retinal detachment: a familial aggregation study.

    Go SL, Hoyng CB, Klaver CC.

    Arch Ophthalmol. 2005 Sep;123(9):1237-41.PMID: 16157805 [PubMed - indexed for MEDLINE]Related articles

    33.

    Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.

    van den Hurk JA, Rashbass P, Roepman R, Davis J, Voesenek KE, Arends ML, Zonneveld MN, van Roekel MH, Cameron K, Rohrschneider K, Heckenlively JR, Koenekoop RK, Hoyng CB, Cremers FP, den Hollander AI.

    Mol Vis. 2005 Apr 15;11:263-73.PMID: 15851977 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

    Zeitz C, Minotti R, Feil S, Mátyás G, Cremers FP, Hoyng CB, Berger W.

    Mol Vis. 2005 Mar 2;11:179-83.PMID: 15761389 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.

    Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, Kellner U, Lorenz B, Salati R, Jurklies B, Farkas A, Andreasson S, Weleber RG, Jacobson SG, Rudolph G, Castellan C, Dollfus H, Legius E, Anastasi M, Bitoun P, Lev D, Sieving PA, Munier FL, Zrenner E, Sharpe LT, Cremers FP, Wissinger B.

    Eur J Hum Genet. 2005 Mar;13(3):302-8.PMID: 15657609 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

    The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.

    Klevering BJ, Deutman AF, Maugeri A, Cremers FP, Hoyng CB.

    Graefes Arch Clin Exp Ophthalmol. 2005 Feb;243(2):90-100. Epub 2004 Dec 22.PMID: 15614537 [PubMed - indexed for MEDLINE]Related articles

    37.

    A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy.

    Maugeri A, Meire F, Hoyng CB, Vink C, Van Regemorter N, Karan G, Yang Z, Cremers FP, Zhang K.

    Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4263-7.PMID: 15557430 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa.

    Klevering BJ, Yzer S, Rohrschneider K, Zonneveld M, Allikmets R, van den Born LI, Maugeri A, Hoyng CB, Cremers FP.

    Eur J Hum Genet. 2004 Dec;12(12):1024-32.PMID: 15494742 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Ocular syphilis acquired through oral sex in two HIV-infected patients.

    McCall MB, van Lith-Verhoeven JJ, van Crevel R, Crama N, Koopmans PP, Hoyng CB, van der Ven AJ.

    Neth J Med. 2004 Jun;62(6):206-8.PMID: 15460502 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    CRB1 mutation spectrum in inherited retinal dystrophies.

    den Hollander AI, Davis J, van der Velde-Visser SD, Zonneveld MN, Pierrottet CO, Koenekoop RK, Kellner U, van den Born LI, Heckenlively JR, Hoyng CB, Handford PA, Roepman R, Cremers FP.

    Hum Mutat. 2004 Nov;24(5):355-69. Review.PMID: 15459956 [PubMed - indexed for MEDLINE]Related articles

    41.

    Identification of novel locus for autosomal dominant butterfly shaped macular dystrophy on 5q21.2-q33.2.

    den Hollander AI, van Lith-Verhoeven JJ, Kersten FF, Heister JG, de Kovel CG, Deutman AF, Hoyng CB, Cremers FP.

    J Med Genet. 2004 Sep;41(9):699-702. No abstract available. PMID: 15342701 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome.

    Theelen T, Go SL, Tilanus MA, Klevering BJ, Deutman AF, Cremers FP, Hoyng CB.

    Graefes Arch Clin Exp Ophthalmol. 2004 Oct;242(10):892-7. Epub 2004 Apr 2.PMID: 15064954 [PubMed - indexed for MEDLINE]Related articles

    43.

    Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.

    Klevering BJ, Maugeri A, Wagner A, Go SL, Vink C, Cremers FP, Hoyng CB.

    Ophthalmology. 2004 Mar;111(3):546-53.PMID: 15019334 [PubMed - indexed for MEDLINE]Related articles

    44.

    Cutaneous vitiligo associated with choroidal hypopigmentation.

    Vingerling JR, Owens S, van der Meijden WI, Hoyng CB, Bird AC.

    Eye (Lond). 2004 Sep;18(9):939-40. No abstract available. PMID: 15002019 [PubMed - indexed for MEDLINE]Related articles

    45.

    Prevalence of remediable disability due to low vision among institutionalised elderly people.

    de Winter LJ, Hoyng CB, Froeling PG, Meulendijks CF, van der Wilt GJ.

    Gerontology. 2004 Mar-Apr;50(2):96-101.PMID: 14963376 [PubMed - indexed for MEDLINE]Related articles

    46.

    The expanding roles of ABCA4 and CRB1 in inherited blindness.

    Cremers FP, Maugeri A, den Hollander AI, Hoyng CB.

    Novartis Found Symp. 2004;255:68-79; discussion 79-84, 177-8.PMID: 14750597 [PubMed - indexed for MEDLINE]Related articles

    47.

    Etanercept in the treatment of patients with primary Sjögren's syndrome: a pilot study.

    Zandbelt MM, de Wilde P, van Damme P, Hoyng CB, van de Putte L, van den Hoogen F.

    J Rheumatol. 2004 Jan;31(1):96-101.PMID: 14705226 [PubMed - indexed for MEDLINE]Related articles

    48.

    The benign concentric annular macular dystrophy locus maps to 6p12.3-q16.

    van Lith-Verhoeven JJ, Hoyng CB, van den Helm B, Deutman AF, Brink HM, Kemperman MH, de Jong WH, Kremer H, Cremers FP.

    Invest Ophthalmol Vis Sci. 2004 Jan;45(1):30-5.PMID: 14691150 [PubMed - indexed for MEDLINE]Related articlesFree article

    49.

    A peculiar autosomal dominant macular dystrophy caused by an asparagine deletion at codon 169 in the peripherin/RDS gene.

    van Lith-Verhoeven JJ, van den Helm B, Deutman AF, Bergen AA, Cremers FP, Hoyng CB, de Jong PT.

    Arch Ophthalmol. 2003 Oct;121(10):1452-7.PMID: 14557182 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

    Jaakson K, Zernant J, Külm M, Hutchinson A, Tonisson N, Glavac D, Ravnik-Glavac M, Hawlina M, Meltzer MR, Caruso RC, Testa F, Maugeri A, Hoyng CB, Gouras P, Simonelli F, Lewis RA, Lupski JR, Cremers FP, Allikmets R.

    Hum Mutat. 2003 Nov;22(5):395-403.PMID: 14517951 [PubMed - indexed for MEDLINE]Related articles

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