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Andrew R Webster

Showing results (91-100 of 372) with videos related to

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Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Investigative Ophthalmology & Visual Science|February 27, 2024
PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum DiseaseMalena Daich Varela, Elena Schiff, Samantha Malka, et al.
Investigative Ophthalmology & Visual Science|January 16, 2014
Vision in observers with enhanced S-cone syndrome: an excess of s-cones but connected mainly to conventional s-cone pathwaysCaterina Ripamonti, Jonathan Aboshiha, G Bruce Henning, et al.
Ophthalmology|August 6, 2023
Coats-like Vasculopathy in Inherited Retinal Disease: Prevalence, Characteristics, Genetics, and ManagementMalena Daich Varela, Giovanni Marco Conti, Samantha Malka, et al.
Ophthalmology|March 5, 2013
A phenotype-genotype correlation study of X-linked retinoschisisAjoy Vincent, Anthony G Robson, Magella M Neveu, et al.
The British Journal of Ophthalmology|October 7, 2018
Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosaGerald Liew, Stacey Strong, Patrick Bradley, et al.
Retina (Philadelphia, Pa.)|April 12, 2021
AN ASSOCIATION BETWEEN STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS, PERIPHERAL RETINOSCHISIS, AND POSTERIOR HYALOID ATTACHMENTEdward Bloch, Blanca Flores-Sánchez, Odysseas Georgiadis, et al.
Ophthalmic Genetics|May 22, 2025
<i>DYRK1A</i> syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotypeSiying Lin, Eleanor Hay, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 20, 2010
Choroidal imaging in inherited retinal disease using the technique of enhanced depth imaging optical coherence tomographyJonathan Yeoh, Waheeda Rahman, Fred Chen, et al.
Pageof 38

Showing results (91-100 of 372) with videos related to

Sort By:
Pageof 38
Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Investigative Ophthalmology & Visual Science|February 27, 2024
PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum DiseaseMalena Daich Varela, Elena Schiff, Samantha Malka, et al.
Investigative Ophthalmology & Visual Science|January 16, 2014
Vision in observers with enhanced S-cone syndrome: an excess of s-cones but connected mainly to conventional s-cone pathwaysCaterina Ripamonti, Jonathan Aboshiha, G Bruce Henning, et al.
Ophthalmology|August 6, 2023
Coats-like Vasculopathy in Inherited Retinal Disease: Prevalence, Characteristics, Genetics, and ManagementMalena Daich Varela, Giovanni Marco Conti, Samantha Malka, et al.
Ophthalmology|March 5, 2013
A phenotype-genotype correlation study of X-linked retinoschisisAjoy Vincent, Anthony G Robson, Magella M Neveu, et al.
The British Journal of Ophthalmology|October 7, 2018
Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosaGerald Liew, Stacey Strong, Patrick Bradley, et al.
Retina (Philadelphia, Pa.)|April 12, 2021
AN ASSOCIATION BETWEEN STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS, PERIPHERAL RETINOSCHISIS, AND POSTERIOR HYALOID ATTACHMENTEdward Bloch, Blanca Flores-Sánchez, Odysseas Georgiadis, et al.
Ophthalmic Genetics|May 22, 2025
<i>DYRK1A</i> syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotypeSiying Lin, Eleanor Hay, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 20, 2010
Choroidal imaging in inherited retinal disease using the technique of enhanced depth imaging optical coherence tomographyJonathan Yeoh, Waheeda Rahman, Fred Chen, et al.
Pageof 38