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1.
Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
Mol Vis
; 28: 57-69, 2022.
Article
in English
| MEDLINE | ID: mdl-35693420
2.
Defects in the Cell Signaling Mediator ß-Catenin Cause the Retinal Vascular Condition FEVR.
Am J Hum Genet
; 100(6): 960-968, 2017 Jun 01.
Article
in English
| MEDLINE | ID: mdl-28575650
3.
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.
Mol Vis
; 21: 236-43, 2015.
Article
in English
| MEDLINE | ID: mdl-25802487
4.
Management of Full-Thickness Macular Hole in A Genetically Confirmed Case with Usher Syndrome.
Ophthalmol Ther
; 9(3): 677-684, 2020 Sep.
Article
in English
| MEDLINE | ID: mdl-32566994
5.
How Successful is Switching from Bevacizumab or Ranibizumab to Aflibercept in Age-Related Macular Degeneration? A Systematic Overview.
Adv Ther
; 36(7): 1532-1548, 2019 07.
Article
in English
| MEDLINE | ID: mdl-31102206
6.
Preservative-free tafluprost/timolol fixed combination: comparative 24-h efficacy administered morning or evening in open-angle glaucoma patients.
Expert Opin Pharmacother
; 19(18): 1981-1988, 2018 Dec.
Article
in English
| MEDLINE | ID: mdl-30328725
7.
Twenty-four-hour intraocular pressure monitoring in normotensive patients undergoing chronic hemodialysis.
Eur J Ophthalmol
; 26(1): 24-9, 2016.
Article
in English
| MEDLINE | ID: mdl-26165324
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