Hoyng CB - Search Results

1

Boon CJ, Klevering BJ, Cremers FP, Zonneveld-Vrieling MN, Theelen T, Den Hollander AI, Hoyng CB. Boon CJ, et al. Among authors: hoyng cb. 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

2

Juvenile atrophy of pigment epithelium and choriocapillaris.

Hoyng C, Pinckers A, Deutman A. Hoyng C, et al. Graefes Arch Clin Exp Ophthalmol. 1992;230(3):230-2. doi: 10.1007/BF00176294. Graefes Arch Clin Exp Ophthalmol. 1992. PMID: 1597287

3

Early findings in central areolar choroidal dystrophy.

Hoyng CB, Pinckers AJ, Deutman AF. Hoyng CB, et al. Acta Ophthalmol (Copenh). 1990 Jun;68(3):356-60. doi: 10.1111/j.1755-3768.1990.tb01940.x. Acta Ophthalmol (Copenh). 1990. PMID: 2392919

4

Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.

Hoyng CB, Heutink P, Testers L, Pinckers A, Deutman AF, Oostra BA. Hoyng CB, et al. Am J Ophthalmol. 1996 Jun;121(6):623-9. doi: 10.1016/s0002-9394(14)70627-0. Am J Ophthalmol. 1996. PMID: 8644804 Free article.

5

The development of central areolar choroidal dystrophy.

Hoyng CB, Deutman AF. Hoyng CB, et al. Graefes Arch Clin Exp Ophthalmol. 1996 Feb;234(2):87-93. doi: 10.1007/BF00695246. Graefes Arch Clin Exp Ophthalmol. 1996. PMID: 8720677 Free article.

6

Genetic fine mapping of the gene for recessive Stargardt disease.

Hoyng CB, Poppelaars F, van de Pol TJ, Kremer H, Pinckers AJ, Deutman AF, Cremers FP. Hoyng CB, et al. Hum Genet. 1996 Oct;98(4):500-4. doi: 10.1007/s004390050247. Hum Genet. 1996. PMID: 8792830 Free article.

7

Central areolar choroidal dystrophy and slowly progressive sensorineural hearing loss.

Hoyng CB, van Rijn PM, Deutman AF. Hoyng CB, et al. Acta Ophthalmol Scand. 1996 Dec;74(6):639-41. doi: 10.1111/j.1600-0420.1996.tb00753.x. Acta Ophthalmol Scand. 1996. PMID: 9017060

8

Visual acuity and scar size in eyes with age-related subfoveal choroidal neovascular lesions, 30 months after radiation therapy.

Bergnik GJ, Hoyng CB, van der Maazen RW, Deutman AF, van Daal WA. Bergnik GJ, et al. Among authors: hoyng cb. Doc Ophthalmol. 1996-1997;92(1):61-75. doi: 10.1007/BF02583278. Doc Ophthalmol. 1996. PMID: 9181334

9

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.

Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Deutman AF, Hoyng CB. Cremers FP, et al. Among authors: hoyng cb. Hum Mol Genet. 1998 Mar;7(3):355-62. doi: 10.1093/hmg/7.3.355. Hum Mol Genet. 1998. PMID: 9466990

10

ABCR unites what ophthalmologists divide(s).

van Driel MA, Maugeri A, Klevering BJ, Hoyng CB, Cremers FP. van Driel MA, et al. Among authors: hoyng cb. Ophthalmic Genet. 1998 Sep;19(3):117-22. doi: 10.1076/opge.19.3.117.2187. Ophthalmic Genet. 1998. PMID: 9810566 Review.

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