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Ophthalmic Genetics|October 13, 2022
Multimodal imaging in Schubert-Bornschein congenital stationary night blindnessMaurizio Battaglia Parodi, Alessandro Arrigo, Firuzeh Rajabian, et al.
Ophthalmic Genetics|November 4, 2022
Melphalan toxicity following treatment of retinoblastoma identified by pattern electroretinogramAlkiviades Liasis, Manuel Paez-Escamilla, Jessi Gruszewski, et al.
Ophthalmic Genetics|April 28, 2016
Vitelliform dystrophies: Prevalence in Olmsted County, Minnesota, United StatesLauren A Dalvin, Jose S Pulido, Alan D Marmorstein
Ophthalmic Genetics|April 21, 2016
Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndromeSeyhan Yazar, Maria Franchina, Jamie E Craig, et al.
Ophthalmic Genetics|February 20, 2016
Topical carbonic anhydrase inhibitors in macular edema associated with Alström syndromePaula Larrañaga-Fragoso, Natalia Pastora, Luciano Bravo-Ljubetic, et al.
Ophthalmic Genetics|May 18, 2016
Ocular findings in a patient with Cockayne syndrome with two mutations in the ERCC6 geneYuan Wu, Yajie Zheng, Xiaoming Yan, et al.
Ophthalmic Genetics|April 1, 2016
Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophyYangfan P Liu, Daniëlle G M Bosch, Anna M Siemiatkowska, et al.
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