| 2023-12 |
Efficacy of part-time patching in preventing recurrence after bilateral lateral rectus recession in children with intermittent exotropia |
BMC Ophthalmology
|
| 2023-12 |
PTPN23 Neurodevelopmental Disorder Presenting With Optic Atrophy and Spasmus Nutans–Like Nystagmus |
JOURNAL OF NEURO-OPHTHALMOLOGY
|
| 2023-11 |
Neuro-Ophthalmic Adverse Events of COVID-19 Infection and Vaccines: A Nationwide Cohort Study |
Investigative Ophthalmology and Visual Science
|
| 2023-10 |
Bickerstaff’s brainstem encephalitis: a rare case of neurologic complication in Ulcerative Colitis |
BMC Neurology
|
| 2023-08 |
Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin |
Frontiers in Genetics
|
| 2023-08 |
Clinical and Genetic Findings in Korean Patients with Choroideremia |
Korean Journal of Ophthalmology
|
| 2023-06 |
The importance of genome sequencing: unraveling SSBP1 variant missed by exome sequencing |
OPHTHALMIC GENETICS
|
| 2023-05 |
Genotypic Profile and Clinical Characteristics of CRX-associated Retinopathy in Koreans |
Genes
|
| 2023-05 |
Correlation between bilateral lateral rectus muscle recession and myopic progression in children with intermittent exotropia |
Scientific Reports
|
| 2023-04 |
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee |
Korean Journal of Ophthalmology
|
| 2023-02 |
Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia |
American Journal of Medical Genetics, Part A
|
| 2023-02 |
Clinical and Genetic Features of Korean Patients with Achromatopsia |
Genes
|
| 2023-01 |
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model
|
International Journal of Molecular Sciences
|
| 2022-12 |
Factors Related to Axial Length Elongation in Myopic Children Who Received 0.05% Atropine Treatment |
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
|
| 2022-09 |
Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study |
Journal of Ophthalmology
|
| 2022-08 |
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy |
Frontiers in Neurology
|
| 2022-06 |
Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy |
Genes
|
| 2022-06 |
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study |
OPHTHALMOLOGY
|
| 2022-06 |
Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus |
Translational Vision Science and Technology
|
| 2022-03 |
Factors Associated With Abducens Nerve Palsy in Patients Undergoing Surgery for Petroclival Meningiomas |
JOURNAL OF NEURO-OPHTHALMOLOGY
|
| 2022-03 |
머리 부분 탑재형 디스플레이를 이용한 입체시검사법 |
대한안과학회지
|
| 2022-01 |
Precision medicine through next-generation sequencing in inherited eye diseases in a Korean cohort |
Genes
|
| 2021-12 |
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients |
Ophthalmology Retina
|
| 2021-11 |
Effectiveness of inferior oblique myectomy in unilateral superior oblique palsy depending on magnitude of hyperdeviation |
대한안과학회지
|
| 2021-10 |
Genetic characteristics and phenotype of korean patients with stickler syndrome: A Korean multicenter analysis report no. 1 |
Genes
|
| 2021-10 |
Clinical utility gene card for FRMD7-related infantile nystagmus |
EUROPEAN JOURNAL OF HUMAN GENETICS
|
| 2021-08 |
Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay |
Korean Journal of Ophthalmology
|
| 2021-08 |
Short Stature With Optic Atrophy and Cone Dystrophy |
JAMA OPHTHALMOLOGY
|
| 2021-07 |
Coats-like Exudative Vitreoretinopathy in NMNAT1 Leber Congenital Amaurosis |
Ophthalmology Retina
|
| 2021-07 |
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features |
CLINICAL GENETICS
|
| 2021-06 |
In Silico identification of a common mobile element insertion in exon 4 of RP1 |
SCIENTIFIC REPORTS
|
| 2021-06 |
Clinical and genetic characteristics of korean congenital stationary night blindness patients |
Genes
|
| 2021-04 |
Retinitis Pigmentosa with Epiretinal Neovascularization at the Macula |
Ophthalmology Retina
|
| 2021-04 |
TUBB3 M323V Syndrome Presents with Infantile Nystagmus |
Genes
|
| 2021-04 |
Nationwide population-based incidence and etiologies of pediatric and adult Horner syndrome |
JOURNAL OF NEUROLOGY
|
| 2021-03 |
RP2 Rod-Cone Dystrophy Causes Spasmus Nutans-Like Nystagmus |
JOURNAL OF NEURO-OPHTHALMOLOGY
|
| 2021-03 |
Aberrant expression of PAX6 gene associated with classical aniridia: identification and functional characterization of novel noncoding mutations |
JOURNAL OF HUMAN GENETICS
|
| 2020-12 |
밀러-피셔증후군과 비커스태프 뇌줄기염의 임상적 특징 |
검안 및 콘택트렌즈학회지
|
| 2020-11 |
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization |
HUMAN MOLECULAR GENETICS
|
| 2020-09 |
Comparison of surgical outcomes between lateral rectus recession and medial rectus advancement for postoperative consecutive exotropia |
MEDICINE
|
| 2020-06 |
편측 상사근마비에서 자기공명영상으로 측정한 상사근 단면적과 임상양상과의 연관성 |
대한안과학회지
|
| 2020-06 |
Accuracy of the Hand-held Wavefront Aberrometer in Measurement of Refractive Error |
Korean Journal of Ophthalmology
|
| 2020-03 |
Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis |
STEM CELL RESEARCH
|
| 2020-03 |
Population-based Incidence of Pediatric and Adult Optic Neuritis and the Risk of Multiple Sclerosis |
OPHTHALMOLOGY
|
| 2020-03 |
Clinical and Optic Disc Characteristics of Patients Showing Visual Recovery in Leber Hereditary Optic Neuropathy |
JOURNAL OF NEURO-OPHTHALMOLOGY
|
| 2020-02 |
Copy number variations and multiallelic variants in Korean patients with leber congenital amaurosis |
MOLECULAR VISION
|
| 2020-02 |
Risk factors associated with poor outcome after medial rectus resection for recurrent intermittent exotropia |
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
|
| 2019-12 |
Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients with Infantile Nystagmus Syndrome |
JAMA OPHTHALMOLOGY
|
| 2019-12 |
Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient |
STEM CELL RESEARCH
|
| 2019-08 |
Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch–Boonstra–Schaaf optic atrophy syndrome |
OPHTHALMIC GENETICS
|
| 2019-08 |
얼굴돌림 및 사시를 동반한 영아안진에서 Adjusted Kestenbaum 술식의 효과 |
대한안과학회지
|
| 2019-06 |
Refractive Outcomes of 4-year-old Children after Intravitreal Anti-VEGF Versus Laser Photocoagulation for Retinopathy of Prematurity |
Korean Journal of Ophthalmology
|
| 2019-03 |
Diagnostic value of ganglion cell-inner plexiform layer for early detection of ethambutol-induced optic neuropathy |
BRITISH JOURNAL OF OPHTHALMOLOGY
|
| 2019-02 |
Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation in a Patient with Hermansky-Pudlak Syndrome and Progressive Pulmonary Fibrosis |
Acute and Critical Care
|
| 2018-12 |
안과 영역에서의 차세대 염기서열 분석 |
검안 및 콘택트렌즈학회지 / Annals of Optometry and Contact Lens
|
| 2018-12 |
Ophthalmoplegia in Mitochondrial Disease |
YONSEI MEDICAL JOURNAL
|
| 2018-09 |
A Young Woman With Acute Visual Loss |
JAMA OPHTHALMOLOGY
|
| 2018-06 |
Low dose versus conventional dose of intravitreal bevacizumab injection for retinopathy of prematurity: a case series with paired-eye comparison |
ACTA OPHTHALMOLOGICA
|
| 2018-05 |
긴장 및 조절 눈모음과다 내사시 환자들에서의 사시 수술 후 결과 |
대한안과학회지
|
| 2017-12 |
Protective effects of biodegradable collagen implants on thinned sclera after strabismus surgery: a paired-eye study |
JOURNAL OF AAPOS
|
| 2017-12 |
Vitreous hemorrhage and Rhegmatogenous retinal detachment that developed after botulinum toxin injection to the extraocular muscle: Case report |
BMC OPHTHALMOLOGY
|
| 2017-12 |
Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome |
JAMA OPHTHALMOLOGY
|
| 2017-11 |
Stroke risk among adult patients with third, fourth or sixth cranial nerve palsy: a Nationwide Cohort Study |
ACTA OPHTHALMOLOGICA
|
| 2017-09 |
Diagnostic application of clinical exome sequencing in Leber congenital amaurosis |
MOLECULAR VISION
|
| 2017-08 |
Retinal microstructures are altered in patients with idiopathic infantile nystagmus |
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
|
| 2017-07 |
Transient neonatal myasthenia gravis due to a mother with ocular onset of anti-muscle specific kinase myasthenia gravis |
NEUROMUSCULAR DISORDERS
|
| 2016-05 |
16프리즘디옵터 이상의 상사시가 동반된 상사근마비에서 2개 근육을 동시 수술한 결과 비교 |
대한안과학회지
|