Detalhe da pesquisa
1.
Long-lived autoreactive memory CD4+ T cells mediate the sustained retinopathy in chronic autoimmune uveitis.
FASEB J
; 37(4): e22855, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36906286
2.
Characterization of Clinical and Immune Responses in an Experimental Chronic Autoimmune Uveitis Model.
Am J Pathol
; 191(3): 425-437, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32966818
3.
Adeno-Associated Virus Serotype 2-hCHM Subretinal Delivery to the Macula in Choroideremia: Two-Year Interim Results of an Ongoing Phase I/II Gene Therapy Trial.
Ophthalmology
; 129(10): 1177-1191, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35714735
4.
Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
Mol Vis
; 26: 423-433, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32565670
5.
Retinal Manifestations in Spinocerebellar Ataxia Type 3.
J Neuroophthalmol
; 2022 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36729871
6.
RTN4IP1-associated non-syndromic optic neuropathy and rod-cone dystrophy.
Ophthalmic Genet
; : 1-5, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38224077
7.
Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor.
Stem Cell Res
; 74: 103280, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38134577
8.
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.
Res Sq
; 2024 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38405922
9.
Disparities in Inherited Retinal Degenerations.
Semin Ophthalmol
; 38(2): 201-206, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36536519
10.
RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHY.
Retin Cases Brief Rep
; 17(5): 533-537, 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37643038
11.
Natural history of retinitis pigmentosa based on genotype, vitamin A/E supplementation, and an electroretinogram biomarker.
JCI Insight
; 8(15)2023 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37261916
12.
KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3.
Br J Ophthalmol
; 2023 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37852740
13.
Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy.
Ophthalmic Genet
; 43(3): 332-339, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35057699
14.
RNA-based therapies in inherited retinal diseases.
Ther Adv Ophthalmol
; 14: 25158414221134602, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36388727
15.
Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind Dogs.
Transl Vis Sci Technol
; 11(5): 24, 2022 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35604672
16.
The Effect of Sample Medication Use on Subsequent Anti-VEGF Agent Selection for Neovascular Age-Related Macular Degeneration.
Semin Ophthalmol
; 37(7-8): 902-908, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35923110
17.
Antisense Oligonucleotide Therapy for Ophthalmic Conditions.
Semin Ophthalmol
; 36(5-6): 452-457, 2021 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34010086
18.
Peripheral Leakage on Ultra-Widefield Fluorescein Angiography in Patients With Inherited Retinal Degeneration.
J Vitreoretin Dis
; 5(2): 147-156, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-37009079
19.
Gene editing technology: Towards precision medicine in inherited retinal diseases.
Semin Ophthalmol
; 36(4): 176-184, 2021 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33621144
20.
Variants of Uncertain Significance: Twins With Identical Pathogenic Gene Mutations in Retinitis Punctata Albescens.
Ophthalmic Surg Lasers Imaging Retina
; 52(8): 450-453, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34410188