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Venki Sundaram

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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.
Ophthalmology|May 15, 2015
Retinal Development in Infants and Young Children with AchromatopsiaHelena Lee, Ravi Purohit, Viral Sheth, et al.
Investigative Ophthalmology & Visual Science|October 4, 2014
Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone healthAdam M Dubis, Robert F Cooper, Jonathan Aboshiha, et al.
Investigative Ophthalmology & Visual Science|August 9, 2014
A prospective longitudinal study of retinal structure and function in achromatopsiaJonathan Aboshiha, Adam M Dubis, Jill Cowing, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Ophthalmology|June 10, 2018
Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular DegenerationManjit S Mehat, Venki Sundaram, Caterina Ripamonti, et al.
The New England Journal of Medicine|May 5, 2015
Long-term effect of gene therapy on Leber's congenital amaurosisJames W B Bainbridge, Manjit S Mehat, Venki Sundaram, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
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.
Ophthalmology|May 15, 2015
Retinal Development in Infants and Young Children with AchromatopsiaHelena Lee, Ravi Purohit, Viral Sheth, et al.
Investigative Ophthalmology & Visual Science|October 4, 2014
Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone healthAdam M Dubis, Robert F Cooper, Jonathan Aboshiha, et al.
Investigative Ophthalmology & Visual Science|August 9, 2014
A prospective longitudinal study of retinal structure and function in achromatopsiaJonathan Aboshiha, Adam M Dubis, Jill Cowing, et al.
Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Ophthalmology|June 10, 2018
Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular DegenerationManjit S Mehat, Venki Sundaram, Caterina Ripamonti, et al.
The New England Journal of Medicine|May 5, 2015
Long-term effect of gene therapy on Leber's congenital amaurosisJames W B Bainbridge, Manjit S Mehat, Venki Sundaram, et al.
Pageof 2