Hoyng CB - Search Results

1

Imaging diabetic retinal disease: clinical imaging requirements.

Schreur V, Larsen MB, Sobrin L, Bhavsar AR, den Hollander AI, Klevering BJ, Hoyng CB, de Jong EK, Grauslund J, Peto T. Schreur V, et al. Among authors: hoyng cb. Acta Ophthalmol. 2022 Nov;100(7):752-762. doi: 10.1111/aos.15110. Epub 2022 Feb 9. Acta Ophthalmol. 2022. PMID: 35142031 Free article. Review.

2

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

3

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

4

Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22.

den Hollander AI, van der Velde-Visser SD, Pinckers AJ, Hoyng CB, Brunner HG, Cremers FP. den Hollander AI, et al. Among authors: hoyng cb. Hum Genet. 1999 Jan;104(1):73-6. doi: 10.1007/s004390050912. Hum Genet. 1999. PMID: 10071195

5

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization.

den Hollander AI, van Driel MA, de Kok YJ, van de Pol DJ, Hoyng CB, Brunner HG, Deutman AF, Cremers FP. den Hollander AI, et al. Among authors: hoyng cb. Genomics. 1999 Jun 15;58(3):240-9. doi: 10.1006/geno.1999.5823. Genomics. 1999. PMID: 10373321

6

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene.

Klevering BJ, van Driel M, van de Pol DJ, Pinckers AJ, Cremers FP, Hoyng CB. Klevering BJ, et al. Among authors: hoyng cb. Br J Ophthalmol. 1999 Aug;83(8):914-8. doi: 10.1136/bjo.83.8.914. Br J Ophthalmol. 1999. PMID: 10413692 Free PMC article.

7

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.

Maugeri A, Klevering BJ, Rohrschneider K, Blankenagel A, Brunner HG, Deutman AF, Hoyng CB, Cremers FP. Maugeri A, et al. Among authors: hoyng cb. Am J Hum Genet. 2000 Oct;67(4):960-6. doi: 10.1086/303079. Epub 2000 Aug 24. Am J Hum Genet. 2000. PMID: 10958761 Free PMC article.

8

Central areolar choroidal dystrophy associated with dominantly inherited drusen.

Klevering BJ, van Driel M, van Hogerwou AJ, van De Pol DJ, Deutman AF, Pinckers AJ, Cremers FP, Hoyng CB. Klevering BJ, et al. Among authors: hoyng cb. Br J Ophthalmol. 2002 Jan;86(1):91-6. doi: 10.1136/bjo.86.1.91. Br J Ophthalmol. 2002. PMID: 11801511 Free PMC article.

9

Phenotypic spectrum of autosomal recessive cone-rod dystrophies caused by mutations in the ABCA4 (ABCR) gene.

Klevering BJ, Blankenagel A, Maugeri A, Cremers FP, Hoyng CB, Rohrschneider K. Klevering BJ, et al. Among authors: hoyng cb. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1980-5. Invest Ophthalmol Vis Sci. 2002. PMID: 12037008

10

[From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].

Cremers FP, Maugeri A, Klevering BJ, Hoefsloot LH, Hoyng CB. Cremers FP, et al. Among authors: hoyng cb. Ned Tijdschr Geneeskd. 2002 Aug 24;146(34):1581-4. Ned Tijdschr Geneeskd. 2002. PMID: 12224481 Review. Dutch.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

417 results

Search Page

Filters