Detalhe da pesquisa
1.
Gene Editing for CEP290-Associated Retinal Degeneration.
N Engl J Med
; 2024 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38709228
2.
Assessment of Visual Function with Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study.
Ophthalmology
; 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38423215
3.
Leber hereditary optic neuropathy gene therapy.
Curr Opin Ophthalmol
; 35(3): 244-251, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38117686
4.
A SYSTEMATIC LITERATURE REVIEW OF DISEASE PROGRESSION REPORTED IN RPGR -ASSOCIATED X-LINKED RETINITIS PIGMENTOSA.
Retina
; 44(1): 1-9, 2024 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37683184
5.
Review of Genotype-Phenotype Correlations in Usher Syndrome.
Ear Hear
; 43(1): 1-8, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34039936
6.
SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY DETECTION OF BRUCH MEMBRANE AND CHORIOCAPILLARIS ABNORMALITIES IN SORSBY MACULAR DYSTROPHY.
Retina
; 42(9): 1645-1654, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35483032
7.
Bilateral visual acuity decline in males with choroideremia: a pooled, cross-sectional meta-analysis.
BMC Ophthalmol
; 22(1): 29, 2022 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35034620
8.
Cavernous Malformation of the Optic Nerve and Chiasm: Prompt Suspicion and Surgery Matter.
J Neuroophthalmol
; 42(1): 108-114, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34001730
9.
Efficacy of Visual Retraining in the Hemianopic Field after Stroke: Results of a Randomized Clinical Trial.
Ophthalmology
; 128(7): 1091-1101, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242498
10.
LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.
Retina
; 41(5): 898-907, 2021 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33595255
11.
Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy.
Int J Mol Sci
; 22(8)2021 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33920085
12.
Chronic condition patterns in the US population and their association with health related quality of life.
Prev Med
; 136: 106102, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32360766
13.
A2E Distribution in RPE Granules in Human Eyes.
Molecules
; 25(6)2020 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32244898
14.
Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease.
Pharm Res
; 36(2): 34, 2019 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30617669
15.
Atypical Late-Onset Leber Hereditary Optic Neuropathy (LHON) Associated With T14484C Mutation.
J Neuroophthalmol
; 44(2): e224-e226, 2024 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38741248
16.
Altered Macular Microvasculature in Mild Cognitive Impairment and Alzheimer Disease.
J Neuroophthalmol
; 38(3): 292-298, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29040211
17.
Gene Therapy for Leber Hereditary Optic Neuropathy: Low- and Medium-Dose Visual Results.
Ophthalmology
; 124(11): 1621-1634, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28647203
18.
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
Retina
; 37(10): 1956-1966, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28145975
19.
Severe Vision Loss and Optic Disc Edema Associated With GAD-65 Antibody Positive Miller Fisher Syndrome.
J Neuroophthalmol
; 2022 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36000786
20.
Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Lancet
; 385(9967): 509-16, 2015 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25458728