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Richard W Yee

Showing results (21-30 of 31) with videos related to

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Cureus|October 16, 2023
Topical Spironolactone in the Treatment of Ocular Graft-Versus-Host DiseaseCalvin W Wong, Annie A Yang, Chia-Yang Liu, et al.
Journal of Cataract and Refractive Surgery|July 5, 2003
Cleavage of corneal basement membrane components by ethanol exposure in laser-assisted subepithelial keratectomyEdgar M Espana, Martin Grueterich, Antonio Mateo, et al.
Investigative Ophthalmology & Visual Science|May 2, 2009
CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosisTimothy T McMahon, Linda S Kim, Gerald A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 19, 2014
Bis(zinc-dipicolylamine), Zn-DPA, a new marker for apoptosisJacky M K Kwong, Celia Hoang, Reshil T Dukes, et al.
The Ocular Surface|October 18, 2024
Mineralocorticoid receptor expression and the effects of the mineralocorticoid receptor antagonist spironolactone in a murine model of graft-versus-host diseaseShinri Sato, Yoko Ogawa, Calvin W Wong, et al.
Cornea|December 18, 2004
Recurrence of chromosome 10 Thiel-Behnke corneal dystrophy (CDB2) after excimer laser phototherapeutic keratectomy or penetrating keratoplastyHani M Sorour, Steven B Yee, Neal J Peterson, et al.
Journal of Clinical Medicine|March 14, 2026
Current Diagnosis and Management of Ocular Graft-Versus-Host Disease at a Tertiary Cancer CenterEesa M Khattak, Nathan A Seto, Calvin W Wong, et al.
Journal of Cataract and Refractive Surgery|December 27, 2006
Excimer laser exacerbation of Avellino corneal dystrophyW Barry Lee, Kenneth S Himmel, Stephen M Hamilton, et al.
Molecular Vision|July 27, 2007
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophyLori S Sullivan, Eric B Baylin, Ramon Font, et al.
Plos One|June 17, 2016
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24Benjamin R Lin, Derek J Le, Yabin Chen, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Cureus|October 16, 2023
Topical Spironolactone in the Treatment of Ocular Graft-Versus-Host DiseaseCalvin W Wong, Annie A Yang, Chia-Yang Liu, et al.
Journal of Cataract and Refractive Surgery|July 5, 2003
Cleavage of corneal basement membrane components by ethanol exposure in laser-assisted subepithelial keratectomyEdgar M Espana, Martin Grueterich, Antonio Mateo, et al.
Investigative Ophthalmology & Visual Science|May 2, 2009
CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosisTimothy T McMahon, Linda S Kim, Gerald A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 19, 2014
Bis(zinc-dipicolylamine), Zn-DPA, a new marker for apoptosisJacky M K Kwong, Celia Hoang, Reshil T Dukes, et al.
The Ocular Surface|October 18, 2024
Mineralocorticoid receptor expression and the effects of the mineralocorticoid receptor antagonist spironolactone in a murine model of graft-versus-host diseaseShinri Sato, Yoko Ogawa, Calvin W Wong, et al.
Cornea|December 18, 2004
Recurrence of chromosome 10 Thiel-Behnke corneal dystrophy (CDB2) after excimer laser phototherapeutic keratectomy or penetrating keratoplastyHani M Sorour, Steven B Yee, Neal J Peterson, et al.
Journal of Clinical Medicine|March 14, 2026
Current Diagnosis and Management of Ocular Graft-Versus-Host Disease at a Tertiary Cancer CenterEesa M Khattak, Nathan A Seto, Calvin W Wong, et al.
Journal of Cataract and Refractive Surgery|December 27, 2006
Excimer laser exacerbation of Avellino corneal dystrophyW Barry Lee, Kenneth S Himmel, Stephen M Hamilton, et al.
Molecular Vision|July 27, 2007
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophyLori S Sullivan, Eric B Baylin, Ramon Font, et al.
Plos One|June 17, 2016
Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24Benjamin R Lin, Derek J Le, Yabin Chen, et al.
Pageof 4