Riise R - Search Results

1

Cataract development in Norwegian patients with congenital aniridia.

Edén U, Lagali N, Dellby A, Utheim TP, Riise R, Chen X, Fagerholm P. Edén U, et al. Among authors: riise r. Acta Ophthalmol. 2014 Mar;92(2):e165-7. doi: 10.1111/aos.12225. Epub 2013 Jul 4. Acta Ophthalmol. 2014. PMID: 23826968 Free PMC article. No abstract available.

2

Aniridia among children and teenagers in Sweden and Norway.

Edén U, Beijar C, Riise R, Tornqvist K. Edén U, et al. Among authors: riise r. Acta Ophthalmol. 2008 Nov;86(7):730-4. doi: 10.1111/j.1755-3768.2008.01310.x. Epub 2008 May 19. Acta Ophthalmol. 2008. PMID: 18494744 Free article.

3

Epidemiology of aniridia in Sweden and Norway.

Edén U, Iggman D, Riise R, Tornqvist K. Edén U, et al. Among authors: riise r. Acta Ophthalmol. 2008 Nov;86(7):727-9. doi: 10.1111/j.1755-3768.2008.01309.x. Epub 2008 May 19. Acta Ophthalmol. 2008. PMID: 18494745 Free article.

4

Corneal involvement in congenital aniridia.

Edén U, Riise R, Tornqvist K. Edén U, et al. Among authors: riise r. Cornea. 2010 Oct;29(10):1096-102. doi: 10.1097/ICO.0b013e3181d20493. Cornea. 2010. PMID: 20567200

5

In vivo morphology of the limbal palisades of vogt correlates with progressive stem cell deficiency in aniridia-related keratopathy.

Lagali N, Edén U, Utheim TP, Chen X, Riise R, Dellby A, Fagerholm P. Lagali N, et al. Among authors: riise r. Invest Ophthalmol Vis Sci. 2013 Aug 7;54(8):5333-42. doi: 10.1167/iovs.13-11780. Invest Ophthalmol Vis Sci. 2013. PMID: 23860752

6

Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort study.

Riise R, Ygge J, Lindman C, Stray-Pedersen A, Bek T, Rødningen OK, Heiberg A. Riise R, et al. Acta Ophthalmol Scand. 2007 Aug;85(5):557-62. doi: 10.1111/j.1600-0420.2007.00890.x. Epub 2007 Mar 22. Acta Ophthalmol Scand. 2007. PMID: 17376192 Free article.

7

Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.

Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R. Grøndahl J, et al. Among authors: riise r. Acta Ophthalmol Scand. 2007 May;85(3):287-97. doi: 10.1111/j.1600-0420.2006.00820.x. Acta Ophthalmol Scand. 2007. PMID: 17488458 Free article.

8

Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.

Selmer KK, Grøndahl J, Riise R, Brandal K, Braaten O, Bragadottir R, Undlien DE. Selmer KK, et al. Among authors: riise r. Acta Ophthalmol. 2010 May;88(3):323-8. doi: 10.1111/j.1755-3768.2008.01465.x. Epub 2009 Jan 30. Acta Ophthalmol. 2010. PMID: 19183411 Free article.

9

Hereditary "ant-egg-cataract".

Riise R. Riise R. Acta Ophthalmol (Copenh). 1967;45(3):341-6. Acta Ophthalmol (Copenh). 1967. PMID: 6072625 No abstract available.

10

"Ant-egg" cataract revisited.

Clemmensen K, Enghild JJ, Ivarsen A, Riise R, Vorum H, Heegaard S. Clemmensen K, et al. Among authors: riise r. Graefes Arch Clin Exp Ophthalmol. 2017 Jan;255(1):119-125. doi: 10.1007/s00417-016-3539-z. Epub 2016 Nov 5. Graefes Arch Clin Exp Ophthalmol. 2017. PMID: 27817115

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