Deutman AF - Search Results

1

Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea.

van Lith-Verhoeven JJ, Cremers FP, van den Helm B, Hoyng CB, Deutman AF. van Lith-Verhoeven JJ, et al. Among authors: deutman af. Mol Vis. 2003 Apr 24;9:138-43. Mol Vis. 2003. PMID: 12724643 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

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. van Lith-Verhoeven JJ, et al. Among authors: deutman af. Invest Ophthalmol Vis Sci. 2004 Jan;45(1):30-5. doi: 10.1167/iovs.03-0392. Invest Ophthalmol Vis Sci. 2004. PMID: 14691150

5

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

6

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.

7

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.

de Brouwer AP, Pennings RJ, Roeters M, Van Hauwe P, Astuto LM, Hoefsloot LH, Huygen PL, van den Helm B, Deutman AF, Bork JM, Kimberling WJ, Cremers FP, Cremers CW, Kremer H. de Brouwer AP, et al. Among authors: deutman af. Hum Genet. 2003 Feb;112(2):156-63. doi: 10.1007/s00439-002-0833-0. Epub 2002 Oct 29. Hum Genet. 2003. PMID: 12522556

8

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

Theelen T, Go SL, Tilanus MA, Klevering BJ, Deutman AF, Cremers FP, Hoyng CB. Theelen T, et al. Among authors: deutman af. Graefes Arch Clin Exp Ophthalmol. 2004 Oct;242(10):892-7. doi: 10.1007/s00417-004-0903-1. Epub 2004 Apr 2. Graefes Arch Clin Exp Ophthalmol. 2004. PMID: 15064954

9

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

Klevering BJ, Deutman AF, Maugeri A, Cremers FP, Hoyng CB. Klevering BJ, et al. Among authors: deutman af. Graefes Arch Clin Exp Ophthalmol. 2005 Feb;243(2):90-100. doi: 10.1007/s00417-004-1079-4. Epub 2004 Dec 22. Graefes Arch Clin Exp Ophthalmol. 2005. PMID: 15614537

10

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

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