Deutman AF - 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: deutman af. 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: deutman af. 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

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. van Lith-Verhoeven JJ, et al. Among authors: deutman af. Arch Ophthalmol. 2003 Oct;121(10):1452-7. doi: 10.1001/archopht.121.10.1452. Arch Ophthalmol. 2003. PMID: 14557182

4

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

5

Congenital arteriovenous communications and the development of two types of leaking retinal macroaneurysms.

Tilanus MD, Hoyng C, Deutman AF, Cruysberg JR, Aandekerk AL. Tilanus MD, et al. Among authors: deutman af. Am J Ophthalmol. 1991 Jul 15;112(1):31-3. doi: 10.1016/s0002-9394(14)76208-7. Am J Ophthalmol. 1991. PMID: 1882918

6

Early findings in central areolar choroidal dystrophy.

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

7

X-linked cone dystrophy. An overlooked diagnosis?

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

8

The development of central areolar choroidal dystrophy.

Hoyng CB, Deutman AF. Hoyng CB, et al. Among authors: deutman af. 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.

9

Central areolar choroidal dystrophy and slowly progressive sensorineural hearing loss.

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

10

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: deutman af. Ophthalmology. 2001 Aug;108(8):1479-84. doi: 10.1016/s0161-6420(01)00640-6. Ophthalmology. 2001. PMID: 11470705

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

160 results

Search Page