Pinckers A - Search Results

1

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. Among authors: pinckers a. 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.

2

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: pinckers aj. 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.

3

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: pinckers aj. 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.

4

Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus.

Driessen CA, Janssen BP, Winkens HJ, Kuhlmann LD, Van Vugt AH, Pinckers AJ, Deutman AF, Janssen JJ. Driessen CA, et al. Among authors: pinckers aj. Ophthalmology. 2001 Aug;108(8):1479-84. doi: 10.1016/s0161-6420(01)00640-6. Ophthalmology. 2001. PMID: 11470705

5

Early findings in central areolar choroidal dystrophy.

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

6

Gyrate atrophy and choroidal neovascularization.

Marano F, Deutman AF, Pinckers AJ, Aandekerk AL. Marano F, et al. Among authors: pinckers aj. Arch Ophthalmol. 1996 Oct;114(10):1295. doi: 10.1001/archopht.1996.01100140495035. Arch Ophthalmol. 1996. PMID: 8859105 Free article. No abstract available.

7

Juvenile atrophy of pigment epithelium and choriocapillaris.

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

8

X-linked cone dystrophy. An overlooked diagnosis?

Pinckers A, Deutman AF. Pinckers A, et al. Int Ophthalmol. 1987 Aug;10(4):241-3. doi: 10.1007/BF00155631. Int Ophthalmol. 1987. PMID: 3498700

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: pinckers aj. Hum Mol Genet. 1998 Mar;7(3):355-62. doi: 10.1093/hmg/7.3.355. Hum Mol Genet. 1998. PMID: 9466990

10

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: pinckers aj. Hum Genet. 1999 Jan;104(1):73-6. doi: 10.1007/s004390050912. Hum Genet. 1999. PMID: 10071195

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