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

Edwin M Stone

Showing results (141-150 of 384) with videos related to

Pageof 39
Sort By:
Journal of Glaucoma|June 16, 2023
Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States PopulationErin A Boese, Wallace L M Alward, Young H Kwon, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|September 15, 2015
Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trialBudd A Tucker, Cathryn M Cranston, Kristin A Anfinson, et al.
Eye (London, England)|July 18, 2018
Evaluation of serum and ocular levels of membrane attack complex and C-reactive protein in CFH-genotyped human donorsKathleen R Chirco, Miles J Flamme-Wiese, Jill S Wiley, et al.
American Journal of Ophthalmology|December 10, 2002
A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutationThomas A Graul, Young H Kwon, M Bridget Zimmerman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2008
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosaJohn H Fingert, Kean Oh, Mina Chung, et al.
American Journal of Ophthalmology|March 17, 2007
Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cuppingRobert A Honkanen, Lee M Jampol, John H Fingert, et al.
Investigative Ophthalmology & Visual Science|August 1, 2013
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1Seongjin Seo, Robert F Mullins, Alina V Dumitrescu, et al.
Investigative Ophthalmology & Visual Science|May 2, 2013
Human photoreceptor outer segments shorten during light adaptationMichael D Abràmoff, Robert F Mullins, Kyungmoo Lee, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Investigative Ophthalmology & Visual Science|February 20, 2014
Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutationsWei Chieh Huang, Artur V Cideciyan, Alejandro J Roman, et al.
Pageof 39

Showing results (141-150 of 384) with videos related to

Sort By:
Pageof 39
Journal of Glaucoma|June 16, 2023
Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States PopulationErin A Boese, Wallace L M Alward, Young H Kwon, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|September 15, 2015
Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trialBudd A Tucker, Cathryn M Cranston, Kristin A Anfinson, et al.
Eye (London, England)|July 18, 2018
Evaluation of serum and ocular levels of membrane attack complex and C-reactive protein in CFH-genotyped human donorsKathleen R Chirco, Miles J Flamme-Wiese, Jill S Wiley, et al.
American Journal of Ophthalmology|December 10, 2002
A case-control comparison of the clinical characteristics of glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutationThomas A Graul, Young H Kwon, M Bridget Zimmerman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2008
Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosaJohn H Fingert, Kean Oh, Mina Chung, et al.
American Journal of Ophthalmology|March 17, 2007
Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cuppingRobert A Honkanen, Lee M Jampol, John H Fingert, et al.
Investigative Ophthalmology & Visual Science|August 1, 2013
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1Seongjin Seo, Robert F Mullins, Alina V Dumitrescu, et al.
Investigative Ophthalmology & Visual Science|May 2, 2013
Human photoreceptor outer segments shorten during light adaptationMichael D Abràmoff, Robert F Mullins, Kyungmoo Lee, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Investigative Ophthalmology & Visual Science|February 20, 2014
Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutationsWei Chieh Huang, Artur V Cideciyan, Alejandro J Roman, et al.
Pageof 39