Detalhe da pesquisa
1.
Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia.
Am J Med Genet A
; 191(2): 582-585, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36367250
2.
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization.
Hum Mol Genet
; 29(18): 2989-3002, 2020 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32744312
3.
Effect of preoperative eyedrops on cytokine concentrations in aqueous humor of patients undergoing femtosecond laser-assisted cataract surgery.
Graefes Arch Clin Exp Ophthalmol
; 260(3): 885-891, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34625847
4.
Aberrant expression of PAX6 gene associated with classical aniridia: identification and functional characterization of novel noncoding mutations.
J Hum Genet
; 66(3): 333-338, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32920601
5.
Pharmacologic properties of high-dose ambroxol in four patients with Gaucher disease and myoclonic epilepsy.
J Med Genet
; 57(2): 124-131, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31649052
6.
Optical Coherence Tomography Angiography Characteristics and Predictors of Visual Outcomes in Patients With Acute and Chronic Nonarteritic Anterior Ischemic Optic Neuropathy.
J Neuroophthalmol
; 41(4): e440-e450, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33110008
7.
Neuro-Ophthalmologic Features and Outcomes of Thalamic Infarction: A Single-Institutional 10-Year Experience.
J Neuroophthalmol
; 41(1): 29-36, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31851027
8.
Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.
Mol Vis
; 26: 26-35, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32165824
9.
Difference in myopia progression between dominant and non-dominant eye in patients with intermittent exotropia.
Graefes Arch Clin Exp Ophthalmol
; 258(6): 1327-1333, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307585
10.
Clinical and Optic Disc Characteristics of Patients Showing Visual Recovery in Leber Hereditary Optic Neuropathy.
J Neuroophthalmol
; 40(1): 15-21, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31609832
11.
PAX6 aniridia syndrome: clinics, genetics, and therapeutics.
Curr Opin Ophthalmol
; 28(5): 436-447, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28598868
12.
The influence of ocular sighting dominance on Fundus torsion in patients with unilateral congenital superior oblique palsy.
Graefes Arch Clin Exp Ophthalmol
; 255(12): 2473-2479, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28823004
13.
First-ever optic neuritis: distinguishing subsequent neuromyelitis optica from multiple sclerosis.
Neurol Sci
; 35(5): 781-3, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24487628
14.
Digital therapeutics using virtual reality-based visual perceptual learning for visual field defects in stroke: A double-blind randomized trial.
Brain Behav
; 14(5): e3525, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38773793
15.
Comparison of OCT measurements between high myopic and low myopic children.
Optom Vis Sci
; 90(12): 1473-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24121408
16.
Clinical and Genetic Features of Korean Patients with Achromatopsia.
Genes (Basel)
; 14(2)2023 02 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36833446
17.
Serum proteins for monitoring and predicting visual function in patients with recent optic neuritis.
Sci Rep
; 13(1): 5609, 2023 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37019946
18.
Comparison between aniridia with and without PAX6 mutations: clinical and molecular analysis in 14 Korean patients with aniridia.
Ophthalmology
; 119(6): 1258-64, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22361317
19.
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy.
Front Neurol
; 13: 978532, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36071901
20.
Relationship between peripapillary atrophy and myopia progression in the eyes of young school children.
Eye (Lond)
; 35(2): 665-671, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32398847