Hoyng CB - Search Results

1

A Deep Learning Model for Segmentation of Geographic Atrophy to Study Its Long-Term Natural History.

Liefers B, Colijn JM, González-Gonzalo C, Verzijden T, Wang JJ, Joachim N, Mitchell P, Hoyng CB, van Ginneken B, Klaver CCW, Sánchez CI. Liefers B, et al. Among authors: hoyng cb. Ophthalmology. 2020 Aug;127(8):1086-1096. doi: 10.1016/j.ophtha.2020.02.009. Epub 2020 Feb 15. Ophthalmology. 2020. PMID: 32197912 Free article.

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

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. Am J Ophthalmol. 1991 Jul 15;112(1):31-3. doi: 10.1016/s0002-9394(14)76208-7. Am J Ophthalmol. 1991. PMID: 1882918

4

Pigmentary irregularities and optic disc edema after heart transplantation.

Klaver CC, Hoyng CB, de Jong PT. Klaver CC, et al. Among authors: hoyng cb. Arch Ophthalmol. 1995 Oct;113(10):1281-5. doi: 10.1001/archopht.1995.01100100069031. Arch Ophthalmol. 1995. PMID: 7575260 Free article.

5

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.

6

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

7

Genetic risk of rhegmatogenous retinal detachment: a familial aggregation study.

Go SL, Hoyng CB, Klaver CC. Go SL, et al. Among authors: hoyng cb. Arch Ophthalmol. 2005 Sep;123(9):1237-41. doi: 10.1001/archopht.123.9.1237. Arch Ophthalmol. 2005. PMID: 16157805

8

Central areolar choroidal dystrophy.

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

9

The spectrum of phenotypes caused by variants in the CFH gene.

Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI. Boon CJ, et al. Among authors: hoyng cb. Mol Immunol. 2009 May;46(8-9):1573-94. doi: 10.1016/j.molimm.2009.02.013. Epub 2009 Mar 17. Mol Immunol. 2009. PMID: 19297022 Review.

10

Genetic etiology and clinical consequences of complete and incomplete achromatopsia.

Thiadens AA, Slingerland NW, Roosing S, van Schooneveld MJ, van Lith-Verhoeven JJ, van Moll-Ramirez N, van den Born LI, Hoyng CB, Cremers FP, Klaver CC. Thiadens AA, et al. Among authors: hoyng cb. Ophthalmology. 2009 Oct;116(10):1984-9.e1. doi: 10.1016/j.ophtha.2009.03.053. Epub 2009 Jul 9. Ophthalmology. 2009. PMID: 19592100

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