Detalhe da pesquisa
1.
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination.
Am J Hum Genet
; 99(2): 470-80, 2016 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486781
2.
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.
Am J Hum Genet
; 99(3): 770-776, 2016 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588451
3.
Efficacy of Topical Nepafenac 0.3% in the Management of Postoperative Cystoid Macular Edema.
Ther Clin Risk Manag
; 16: 1067-1074, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33192068
4.
Optical Biometry Derived Axial Length Measurements Following Intravitreal Anti-Vascular Endothelial Growth Factor Treatment for Macular Edema.
Semin Ophthalmol
; 33(4): 488-491, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-28402713
5.
Evaluation of corneal stromal demarcation line depth following standard and a modified-accelerated collagen cross-linking protocol.
Am J Ophthalmol
; 158(4): 671-675.e1, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25034113
6.
Corneal Imaging Abnormalities in Familial Keratoconus.
J Refract Surg
; 33(1): 62-63, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28068450