Search research articles
Contact Us
Filters
Showing results (11-20 of 15) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 15 results.
Ophthalmology
|
January 3, 2021
Reducing the Global Burden of Myopia by Delaying the Onset of Myopia and Reducing Myopic Progression in Children: The Academy's Task Force on Myopia
Bobeck S Modjtahedi, Richard L Abbott, Donald S Fong, et al.
BMC Ophthalmology
|
May 27, 2005
Primary graft failure associated with epithelial downgrowth: a case report
Anthony J Aldave, David A Hollander, Bruno Branco, et al.
Cornea
|
February 27, 2003
Spontaneous corneal hydrops and perforation in keratoconus and pellucid marginal degeneration
Anthony J Aldave, Michele Mabon, David A Hollander, et al.
American Journal of Ophthalmology
|
November 5, 2003
A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I
John F Warren, Richard L Abbott, Michael K Yoon, et al.
American Journal of Ophthalmology
|
August 12, 2018
The Asia Cornea Society Infectious Keratitis Study: A Prospective Multicenter Study of Infectious Keratitis in Asia
Wei-Boon Khor, Venkatesh N Prajna, Prashant Garg, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Ophthalmology
|
January 3, 2021
Reducing the Global Burden of Myopia by Delaying the Onset of Myopia and Reducing Myopic Progression in Children: The Academy's Task Force on Myopia
Bobeck S Modjtahedi, Richard L Abbott, Donald S Fong, et al.
BMC Ophthalmology
|
May 27, 2005
Primary graft failure associated with epithelial downgrowth: a case report
Anthony J Aldave, David A Hollander, Bruno Branco, et al.
Cornea
|
February 27, 2003
Spontaneous corneal hydrops and perforation in keratoconus and pellucid marginal degeneration
Anthony J Aldave, Michele Mabon, David A Hollander, et al.
American Journal of Ophthalmology
|
November 5, 2003
A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I
John F Warren, Richard L Abbott, Michael K Yoon, et al.
American Journal of Ophthalmology
|
August 12, 2018
The Asia Cornea Society Infectious Keratitis Study: A Prospective Multicenter Study of Infectious Keratitis in Asia
Wei-Boon Khor, Venkatesh N Prajna, Prashant Garg, et al.
Page
of 2