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Cureus
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October 16, 2023
Topical Spironolactone in the Treatment of Ocular Graft-Versus-Host Disease
Calvin 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 keratectomy
Edgar 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 amaurosis
Timothy 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 apoptosis
Jacky 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 disease
Shinri 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 keratoplasty
Hani 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 Center
Eesa 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 dystrophy
W 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 dystrophy
Lori 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-q24
Benjamin R Lin, Derek J Le, Yabin Chen, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Cureus
|
October 16, 2023
Topical Spironolactone in the Treatment of Ocular Graft-Versus-Host Disease
Calvin 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 keratectomy
Edgar 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 amaurosis
Timothy 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 apoptosis
Jacky 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 disease
Shinri 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 keratoplasty
Hani 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 Center
Eesa 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 dystrophy
W 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 dystrophy
Lori 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-q24
Benjamin R Lin, Derek J Le, Yabin Chen, et al.
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of 4