Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Samuel G Jacobson

Showing results (21-30 of 224) with videos related to

Pageof 23
Sort By:
Ophthalmology|July 3, 2002
Early age-related maculopathy and self-reported visual difficulty in daily lifeKay Scilley, Gregory R Jackson, Artur V Cideciyan, et al.
Experimental Eye Research|July 20, 2002
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotypeTomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, et al.
BMC Ophthalmology|August 9, 2015
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrastAlejandro J Roman, Artur V Cideciyan, Rodrigo Matsui, et al.
Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.
American Journal of Human Genetics|June 22, 2002
Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsiaSusanne Kohl, Britta Baumann, Thomas Rosenberg, et al.
Investigative Ophthalmology & Visual Science|January 24, 2013
Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutationsAlejandro J Roman, Artur V Cideciyan, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Human Molecular Genetics|April 3, 2009
Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetateTadao Maeda, Artur V Cideciyan, Akiko Maeda, et al.
Investigative Ophthalmology & Visual Science|September 13, 2018
Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 YearsArtur V Cideciyan, Jason Charng, Alejandro J Roman, et al.
Pageof 23

Showing results (21-30 of 224) with videos related to

Sort By:
Pageof 23
Ophthalmology|July 3, 2002
Early age-related maculopathy and self-reported visual difficulty in daily lifeKay Scilley, Gregory R Jackson, Artur V Cideciyan, et al.
Experimental Eye Research|July 20, 2002
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotypeTomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, et al.
BMC Ophthalmology|August 9, 2015
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrastAlejandro J Roman, Artur V Cideciyan, Rodrigo Matsui, et al.
Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.
American Journal of Human Genetics|June 22, 2002
Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsiaSusanne Kohl, Britta Baumann, Thomas Rosenberg, et al.
Investigative Ophthalmology & Visual Science|January 24, 2013
Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutationsAlejandro J Roman, Artur V Cideciyan, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Human Molecular Genetics|April 3, 2009
Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetateTadao Maeda, Artur V Cideciyan, Akiko Maeda, et al.
Investigative Ophthalmology & Visual Science|September 13, 2018
Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 YearsArtur V Cideciyan, Jason Charng, Alejandro J Roman, et al.
Pageof 23