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Ophthalmic genetics

Showing results (1-10 of 2,048) with videos related to

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Ophthalmic Genetics|October 14, 2022
Readability, Content, and Accountability Assessment of Online Health Information for Retinitis Pigmentosa & Retinitis Pigmentosa Treatment OptionsStacy Partin, Eleanor Westfall, Gregory Sanda, et al.
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|September 3, 2015
Association between the CDKN2B-AS1 Gene and Primary Open Angle Glaucoma with High Myopia in Japanese PatientsYugo Kimura, Tadamichi Akagi, Masahiro Miyake, 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|March 12, 2016
Novel mutations in the L visual pigment gene found in Japanese men with protan color-vision defect having a normal order L/M gene arraySanae Muraki, Hisao Ueyama, Shoko Tanabe, 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|February 23, 2016
Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45Mélanie Fradin, Estelle Colin, Daniele Hannouche-Bared, et al.
Ophthalmic Genetics|March 5, 2016
Evaluation of C-reactive protein and CC-cytokine ligand 2 polymorphism interaction for age-related macular degenerationMohammad Hossein Jabbarpoor Bonyadi, Tahereh Mohammadian, Mortaza Bonyadi, et al.
Pageof 205

Showing results (1-10 of 2,048) with videos related to

Sort By:
Pageof 205
Ophthalmic Genetics|October 14, 2022
Readability, Content, and Accountability Assessment of Online Health Information for Retinitis Pigmentosa & Retinitis Pigmentosa Treatment OptionsStacy Partin, Eleanor Westfall, Gregory Sanda, et al.
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|September 3, 2015
Association between the CDKN2B-AS1 Gene and Primary Open Angle Glaucoma with High Myopia in Japanese PatientsYugo Kimura, Tadamichi Akagi, Masahiro Miyake, 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|March 12, 2016
Novel mutations in the L visual pigment gene found in Japanese men with protan color-vision defect having a normal order L/M gene arraySanae Muraki, Hisao Ueyama, Shoko Tanabe, 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|February 23, 2016
Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45Mélanie Fradin, Estelle Colin, Daniele Hannouche-Bared, et al.
Ophthalmic Genetics|March 5, 2016
Evaluation of C-reactive protein and CC-cytokine ligand 2 polymorphism interaction for age-related macular degenerationMohammad Hossein Jabbarpoor Bonyadi, Tahereh Mohammadian, Mortaza Bonyadi, et al.
Pageof 205