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Gerald A Fishman

Showing results (141-150 of 176) with videos related to

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Retina (Philadelphia, Pa.)|January 29, 2011
Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patientsTyson R Kinnick, Robert F Mullins, Sundeep Dev, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
Translational Vision Science & Technology|January 29, 2021
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in AchromatopsiaKatie M Litts, Erica N Woertz, Michalis Georgiou, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Ophthalmology Science|April 28, 2025
Longitudinal Imaging of the Parafoveal Cone Mosaic in Congenital AchromatopsiaNickolas Chen, Katie M Litts, Danica Nikezic, et al.
Molecular Vision|April 28, 2021
Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerationsGang Zou, Tao Zhang, Xuesen Cheng, 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|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Plos Genetics|March 30, 2022
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 diseaseJana Zernant, Winston Lee, Jun Wang, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosisSuzanne Yzer, Gerald A Fishman, Julie Racine, et al.
Pageof 18

Showing results (141-150 of 176) with videos related to

Sort By:
Pageof 18
Retina (Philadelphia, Pa.)|January 29, 2011
Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patientsTyson R Kinnick, Robert F Mullins, Sundeep Dev, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
Translational Vision Science & Technology|January 29, 2021
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in AchromatopsiaKatie M Litts, Erica N Woertz, Michalis Georgiou, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Ophthalmology Science|April 28, 2025
Longitudinal Imaging of the Parafoveal Cone Mosaic in Congenital AchromatopsiaNickolas Chen, Katie M Litts, Danica Nikezic, et al.
Molecular Vision|April 28, 2021
Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerationsGang Zou, Tao Zhang, Xuesen Cheng, 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|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Plos Genetics|March 30, 2022
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 diseaseJana Zernant, Winston Lee, Jun Wang, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosisSuzanne Yzer, Gerald A Fishman, Julie Racine, et al.
Pageof 18