Detalhe da pesquisa
1.
CELLULAR IMAGING OF THE TAPETAL-LIKE REFLEX IN CARRIERS OF RPGR-ASSOCIATED RETINOPATHY.
Retina
; 39(3): 570-580, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29190250
2.
Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Ophthalmology
; 125(5): 735-746, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29310964
3.
QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY.
Retina
; 38(12): 2401-2414, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29016458
4.
Reliability of retinal vessel calibre measurements using a retinal oximeter.
BMC Ophthalmol
; 15: 184, 2015 Dec 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26705024
5.
Comparison of Two Formulas Used to Calculate Summarized Retinal Vessel Calibers.
Optom Vis Sci
; 92(11): 1085-91, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26390347
6.
Adaptive Optics Retinal Imaging in RDH12-Associated Early Onset Severe Retinal Dystrophy.
Invest Ophthalmol Vis Sci
; 65(3): 9, 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38466282
7.
In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods Study.
Transl Vis Sci Technol
; 13(4): 14, 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38591946
8.
Structural and functional characterization of an individual with the M285R KCNV2 hypomorphic allele.
Ophthalmic Genet
; : 1-10, 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38454848
9.
Deep phenotyping of PROM1-associated retinal degeneration.
Br J Ophthalmol
; 108(4): 558-565, 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37080590
10.
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes.
Prog Retin Eye Res
; 100: 101244, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38278208
11.
Retinal vessel tortuosity measures and their applications.
Exp Eye Res
; 106: 40-6, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23146682
12.
Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration.
Am J Ophthalmol
; 252: 77-93, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36948373
13.
First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated Achromatopsia.
Am J Ophthalmol
; 253: 243-251, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37172884
14.
Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts.
Ophthalmic Genet
; 43(2): 218-223, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34748434
15.
Novel disease-causing variant in RDH12 presenting with autosomal dominant retinitis pigmentosa.
Br J Ophthalmol
; 106(9): 1274-1281, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34031043
16.
Investigation of PTC124-mediated translational readthrough in a retinal organoid model of AIPL1-associated Leber congenital amaurosis.
Stem Cell Reports
; 17(10): 2187-2202, 2022 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36084639
17.
Foveal Cone Structure in Patients With Blue Cone Monochromacy.
Invest Ophthalmol Vis Sci
; 63(11): 23, 2022 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36301530
18.
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal Diseases.
Invest Ophthalmol Vis Sci
; 63(6): 15, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35704304
19.
Agreement Between Spectral-Domain and Swept-Source Optical Coherence Tomography Retinal Thickness Measurements in Macular and Retinal Disease.
Ophthalmol Ther
; 10(4): 913-922, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34324166
20.
Comparing Retinal Structure in Patients with Achromatopsia and Blue Cone Monochromacy Using OCT.
Ophthalmol Sci
; 1(3)2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36186895