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Stephen Tsang

Showing results (11-20 of 27) with videos related to

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Advances in Experimental Medicine and Biology|July 30, 2025
Inborn Errors of Metabolism: Refsum DiseaseSitara Hirji, Stephen Tsang, Tarun Sharma, et al.
Ophthalmic Genetics|November 12, 2010
Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3Krishna Mukkamala, Ronald C Gentile, Judith Willner, et al.
Journal of Neuroscience Research|April 28, 2018
Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt diseaseMaarjaliis Paavo, Winston Lee, Rando Allikmets, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 21, 2015
Resolution of foveal schisis in X-linked retinoschisis in the setting of retinal detachmentMrinali Patel Gupta, George Parlitsis, Stephen Tsang, et al.
Retina (Philadelphia, Pa.)|April 17, 2023
Foveal Development and Posterior Precortical Vitreous Pocket FormationDaniel Oh, Juliet Esselfie, Stephen Tsang, et al.
Retinal Cases & Brief Reports|November 13, 2014
Electroretinography and microperimetry as noninvasive diagnostic tools for cilioretinal artery occlusionSamir R Tari, Vivienne C Greenstein, Stephen Tsang, et al.
Advances in Experimental Medicine and Biology|July 30, 2025
Ciliopathy: Bardet-Biedl SyndromeAhmet Hondur, Stephen Tsang, Alicia R P Aycinena, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 28, 2015
Recessive Stargardt disease phenocopying hydroxychloroquine retinopathyKalev Nõupuu, Winston Lee, Jana Zernant, et al.
Retina (Philadelphia, Pa.)|May 17, 2013
Outer retinal tubulation in degenerative retinal disordersNaomi R Goldberg, Jonathan P Greenberg, Ketan Laud, et al.
American Journal of Ophthalmology Case Reports|June 14, 2019
Utility of <i>en-face</i> imaging in diagnosis of occult macular dystrophy with RP1L1 mutation: A case seriesMerry Zc Ruan, S Amal Hussnain, Amanda Thomas, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Advances in Experimental Medicine and Biology|July 30, 2025
Inborn Errors of Metabolism: Refsum DiseaseSitara Hirji, Stephen Tsang, Tarun Sharma, et al.
Ophthalmic Genetics|November 12, 2010
Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3Krishna Mukkamala, Ronald C Gentile, Judith Willner, et al.
Journal of Neuroscience Research|April 28, 2018
Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt diseaseMaarjaliis Paavo, Winston Lee, Rando Allikmets, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 21, 2015
Resolution of foveal schisis in X-linked retinoschisis in the setting of retinal detachmentMrinali Patel Gupta, George Parlitsis, Stephen Tsang, et al.
Retina (Philadelphia, Pa.)|April 17, 2023
Foveal Development and Posterior Precortical Vitreous Pocket FormationDaniel Oh, Juliet Esselfie, Stephen Tsang, et al.
Retinal Cases & Brief Reports|November 13, 2014
Electroretinography and microperimetry as noninvasive diagnostic tools for cilioretinal artery occlusionSamir R Tari, Vivienne C Greenstein, Stephen Tsang, et al.
Advances in Experimental Medicine and Biology|July 30, 2025
Ciliopathy: Bardet-Biedl SyndromeAhmet Hondur, Stephen Tsang, Alicia R P Aycinena, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 28, 2015
Recessive Stargardt disease phenocopying hydroxychloroquine retinopathyKalev Nõupuu, Winston Lee, Jana Zernant, et al.
Retina (Philadelphia, Pa.)|May 17, 2013
Outer retinal tubulation in degenerative retinal disordersNaomi R Goldberg, Jonathan P Greenberg, Ketan Laud, et al.
American Journal of Ophthalmology Case Reports|June 14, 2019
Utility of <i>en-face</i> imaging in diagnosis of occult macular dystrophy with RP1L1 mutation: A case seriesMerry Zc Ruan, S Amal Hussnain, Amanda Thomas, et al.
Pageof 3