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Gerald A Fishman

Showing results (151-160 of 176) with videos related to

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Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Translational Vision Science & Technology|March 17, 2016
Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt DiseaseMoataz M Razeen, Robert F Cooper, Christopher S Langlo, et al.
Investigative Ophthalmology & Visual Science|May 31, 2002
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseasesDror Sharon, Hiroyuki Yamamoto, Terri L McGee, et al.
Current Eye Research|February 29, 2020
Interocular Symmetry of Foveal Cone Topography in Congenital AchromatopsiaKatie M Litts, Michalis Georgiou, Christopher S Langlo, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneTomas R Burke, Gerald A Fishman, Jana Zernant, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Pageof 18

Showing results (151-160 of 176) with videos related to

Sort By:
Pageof 18
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Translational Vision Science & Technology|March 17, 2016
Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt DiseaseMoataz M Razeen, Robert F Cooper, Christopher S Langlo, et al.
Investigative Ophthalmology & Visual Science|May 31, 2002
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseasesDror Sharon, Hiroyuki Yamamoto, Terri L McGee, et al.
Current Eye Research|February 29, 2020
Interocular Symmetry of Foveal Cone Topography in Congenital AchromatopsiaKatie M Litts, Michalis Georgiou, Christopher S Langlo, et al.
Journal of Medical Genetics|May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient populationGail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneTomas R Burke, Gerald A Fishman, Jana Zernant, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathyTomas S Aleman, Nagasamy Soumittra, Artur V Cideciyan, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Pageof 18