Detalhe da pesquisa
1.
Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of PRDM13 causing North Carolina macular dystrophy in Korea.
Mol Vis
; 30: 58-66, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38601016
2.
Prognostic factors of first-onset optic neuritis based on diagnostic criteria and antibody status: a multicentre analysis of 427 eyes.
J Neurol Neurosurg Psychiatry
; 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38418215
3.
Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea.
Neurol Sci
; 45(3): 1173-1183, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37853292
4.
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
5.
Bickerstaff's brainstem encephalitis: a rare case of neurologic complication in Ulcerative Colitis.
BMC Neurol
; 23(1): 386, 2023 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37884876
6.
Efficacy of part-time patching in preventing recurrence after bilateral lateral rectus recession in children with intermittent exotropia.
BMC Ophthalmol
; 23(1): 510, 2023 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38098018
7.
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model.
Int J Mol Sci
; 24(2)2023 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36674802
8.
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
9.
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Ophthalmology
; 129(6): 708-718, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35157951
10.
Factors Associated With Abducens Nerve Palsy in Patients Undergoing Surgery for Petroclival Meningiomas.
J Neuroophthalmol
; 42(1): e209-e216, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34974485
11.
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
12.
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
13.
Population-based Incidence of Pediatric and Adult Optic Neuritis and the Risk of Multiple Sclerosis.
Ophthalmology
; 127(3): 417-425, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31732227
14.
Risk factors associated with poor outcome after medial rectus resection for recurrent intermittent exotropia.
Graefes Arch Clin Exp Ophthalmol
; 258(2): 445-450, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31741045
15.
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
16.
PTPN23 Neurodevelopmental Disorder Presenting With Optic Atrophy and Spasmus Nutans-Like Nystagmus.
J Neuroophthalmol
; 43(4): e316-e318, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35427297
17.
Diagnostic application of clinical exome sequencing in Leber congenital amaurosis.
Mol Vis
; 23: 649-659, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28966547
18.
Retinal microstructures are altered in patients with idiopathic infantile nystagmus.
Graefes Arch Clin Exp Ophthalmol
; 255(8): 1661-1668, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28616716
19.
Vitreous hemorrhage and Rhegmatogenous retinal detachment that developed after botulinum toxin injection to the extraocular muscle: case report.
BMC Ophthalmol
; 17(1): 249, 2017 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29237498
20.
Retinal Artery Occlusion and the Risk of Stroke Development: Twelve-Year Nationwide Cohort Study.
Stroke
; 47(2): 376-82, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26742801