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Ophthalmic Genetics|February 2, 2018
The distinct optic disk and peripapillary appearance in Donnai-Barrow syndromeArif O Khan, Nicola G GhaziOphthalmic Genetics|November 4, 2017
Successful conservative treatment of massive choroidal relapse in 2 retinoblastoma patients monitored by ultrasound biomicroscopy and/or spectral domain optic coherence tomographyChristina Stathopoulos, Marie-Claire Gaillard, Francesco Puccinelli, et al.Ophthalmic Genetics|November 8, 2017
A new perspective on the genetics of keratoconus: why have we not been more successful?Hanne Valgaeren, Carina Koppen, Guy Van CampOphthalmic Genetics|December 28, 2018
Early posterior vitreous detachment is associated with LAMA5 dominant mutationFilomena Napolitano, Valentina Di Iorio, Giuseppe Di Iorio, et al.Ophthalmic Genetics|February 10, 2018
OCT-guided management of subclinical recurrent retinoblastomaMarie-Claire Gaillard, Susan Houghton, Christina Stathopoulos, et al.Ophthalmic Genetics|September 27, 2007
PAX6 mutations may be associated with high myopiaAlex W Hewitt, Lisa S Kearns, Robyn V Jamieson, et al.Ophthalmic Genetics|September 4, 2008
Familial aortic dissection and congenital iris flocculi with hypertensionPrasit Phowthongkum, Patinut Burapasubkajorn, Pongsak Intarabeth, et al.Ophthalmic Genetics|September 4, 2008
Bardet-biedl syndrome: an atypical phenotype in brothers with a proven BBS1 mutationPaul S Cannon, Jill Clayton-Smith, Philip L Beales, et al.Ophthalmic Genetics|September 4, 2008
Mutation analysis of the VMD2 gene in thai families with best macular dystrophyLa-ongsri Atchaneeyasakul, Worapoj Jinda, Natta Sakolsatayadorn, et al.Ophthalmic Genetics|December 7, 2006
From vivarium to bedside: lessons learned from animal modelsEwa Budzynski, Yongsuk Lee, Kenji Sakamoto, et al.Pageof 185