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

John H Fingert

Showing results (31-40 of 135) with videos related to

Pageof 14
Sort By:
Vision Research|August 16, 2024
Minimal phenotypes in transgenic mice with the human LOXL1/LOXL1-AS1 locus associated with exfoliation glaucomaKacie J Meyer, Hannah E Mercer, Ben R Roos, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
American Journal of Ophthalmology|February 24, 2019
The Heritability of Pigment Dispersion Syndrome and Pigmentary GlaucomaAnamika Tandon, Ze Zhang, John H Fingert, et al.
Ophthalmic Genetics|May 11, 2010
Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmusJohn H Fingert, Ben Roos, Mari E Eyestone, et al.
Journal of Glaucoma|March 8, 2016
The Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis PatientsJustin M Risma, Shandiz Tehrani, Kai Wang, et al.
Journal of Glaucoma|April 25, 2012
Circumferential iris transillumination defects in exfoliation syndromeJohn H Fingert, James H Burden, Kai Wang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 10, 2006
Case of Stargardt disease caused by uniparental isodisomyJohn H Fingert, David A Eliason, Nicole C Phillips, et al.
Ophthalmology|December 24, 2023
The Effect of Insurance Coverage Laws on Glaucoma Eyedrop Medication UsageNicole Hehr, Patrick B Barlow, Wisam Najdawi, et al.
Current Eye Research|July 31, 2019
Novel Intragenic <i>PAX6</i> Deletion in a Pedigree with Aniridia, Morbid Obesity, and DiabetesErin A Boese, Mallory R Tollefson, Michael J Schnieders, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Pageof 14

Showing results (31-40 of 135) with videos related to

Sort By:
Pageof 14
Vision Research|August 16, 2024
Minimal phenotypes in transgenic mice with the human LOXL1/LOXL1-AS1 locus associated with exfoliation glaucomaKacie J Meyer, Hannah E Mercer, Ben R Roos, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
American Journal of Ophthalmology|February 24, 2019
The Heritability of Pigment Dispersion Syndrome and Pigmentary GlaucomaAnamika Tandon, Ze Zhang, John H Fingert, et al.
Ophthalmic Genetics|May 11, 2010
Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmusJohn H Fingert, Ben Roos, Mari E Eyestone, et al.
Journal of Glaucoma|March 8, 2016
The Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis PatientsJustin M Risma, Shandiz Tehrani, Kai Wang, et al.
Journal of Glaucoma|April 25, 2012
Circumferential iris transillumination defects in exfoliation syndromeJohn H Fingert, James H Burden, Kai Wang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 10, 2006
Case of Stargardt disease caused by uniparental isodisomyJohn H Fingert, David A Eliason, Nicole C Phillips, et al.
Ophthalmology|December 24, 2023
The Effect of Insurance Coverage Laws on Glaucoma Eyedrop Medication UsageNicole Hehr, Patrick B Barlow, Wisam Najdawi, et al.
Current Eye Research|July 31, 2019
Novel Intragenic <i>PAX6</i> Deletion in a Pedigree with Aniridia, Morbid Obesity, and DiabetesErin A Boese, Mallory R Tollefson, Michael J Schnieders, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Pageof 14