Browsing "1. Journal Papers" by Author : 4180

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Issue DateTitleJournal Title
201616프리즘디옵터 이상의 상사시가 동반된 상사근마비에서 2개 근육을 동시 수술한 결과 비교 JOURNAL OF THE KOREAN OPHTHALMOLOGICAL SOCIETY
2018A Young Woman With Acute Visual Loss.JAMA OPHTHALMOLOGY
2021Aberrant expression of PAX6 gene associated with classical aniridia: identification and functional characterization of novel noncoding mutationsJOURNAL OF HUMAN GENETICS
2017Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus SyndromeJAMA OPHTHALMOLOGY
2020Accuracy of the Hand-held Wavefront Aberrometer in Measurement of Refractive Error Korean Journal of Ophthalmology
2016Anterior nasal transposition of the inferior oblique muscle can cause antielevation syndromeJOURNAL OF AAPOS
2023Bickerstaff's brainstem encephalitis: a rare case of neurologic complication in Ulcerative Colitis BMC NEUROLOGY
2014Changes in fusional vergence amplitudes after laser refractive surgery for moderate myopia.JOURNAL OF CATARACT AND REFRACTIVE SURGERY
2014Changes in the accommodation-convergence relationship after the Artisan phakic intraocular lens implantation for myopic patients Korean Journal of Ophthalmology
2022Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study JOURNAL OF OPHTHALMOLOGY
2021Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients GENES
2023Clinical and Genetic Features of Korean Patients with AchromatopsiaGENES
2023Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin FRONTIERS IN GENETICS
2023Clinical and Genetic Findings in Korean Patients with Choroideremia Korean Journal of Ophthalmology
2020Clinical and Optic Disc Characteristics of Patients Showing Visual Recovery in Leber Hereditary Optic NeuropathyJOURNAL OF NEURO-OPHTHALMOLOGY
2022Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy GENES
2021Clinical utility gene card for FRMD7-related infantile nystagmusEUROPEAN JOURNAL OF HUMAN GENETICS
2021Coats-like Exudative Vitreoretinopathy in NMNAT1 Leber Congenital AmaurosisOPHTHALMOLOGY RETINA
2020Comparison of surgical outcomes between lateral rectus recession and medial rectus advancement for postoperative consecutive exotropia MEDICINE
2020Copy Number Variations and Multiallelic Variants in Korean Patients With Leber Congenital Amaurosis MOLECULAR VISION
2023Correlation between bilateral lateral rectus muscle recession and myopic progression in children with intermittent exotropia SCIENTIFIC REPORTS
2017Diagnostic application of clinical exome sequencing in Leber congenital amaurosis MOLECULAR VISION
2019Diagnostic value of ganglion cell-inner plexiform layer for early detection of ethambutol-induced optic neuropathyBRITISH JOURNAL OF OPHTHALMOLOGY
2021DYNC2H1 variants cause Leber congenital amaurosis without syndromic featuresCLINICAL GENETICS
2016Ecchordosis physaliphora presenting with abducens nerve palsyJOURNAL OF AAPOS
2023Efficacy of part-time patching in preventing recurrence after bilateral lateral rectus recession in children with intermittent exotropia BMC OPHTHALMOLOGY
2023Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegiaAMERICAN JOURNAL OF MEDICAL GENETICS PART A
2019Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation in a Patient with Hermansky-Pudlak Syndrome and Progressive Pulmonary Fibrosis Acute and Critical Care
2022Factors Associated With Abducens Nerve Palsy in Patients Undergoing Surgery for Petroclival MeningiomasJOURNAL OF NEURO-OPHTHALMOLOGY
2022Factors Related to Axial Length Elongation in Myopic Children Who Received 0.05% Atropine TreatmentJOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
2020Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis STEM CELL RESEARCH
2019Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient STEM CELL RESEARCH
2021Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1 GENES
2022Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy FRONTIERS IN NEUROLOGY
2021Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese PatientsOPHTHALMOLOGY RETINA
2022Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study OPHTHALMOLOGY
2023Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans GENES
2021In Silico identification of a common mobile element insertion in exon 4 of RP1 SCIENTIFIC REPORTS
2013Linezolid-Associated Optic Neuropathy in a Patient With Drug-Resistant TuberculosisJOURNAL OF NEURO-OPHTHALMOLOGY
2015Longitudinal analysis of retinal nerve fiber layer and ganglion cell-inner plexiform layer thickness in ethambutol-induced optic neuropathyGRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
2018Low dose versus conventional dose of intravitreal bevacizumab injection for retinopathy of prematurity: a case series with paired-eye comparisonACTA OPHTHALMOLOGICA
2019Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome JAMA OPHTHALMOLOGY
2021Nationwide population-based incidence and etiologies of pediatric and adult Horner syndromeJOURNAL OF NEUROLOGY
2011Negative refraction power causes underestimation of peripapillary retinal nerve fibre layer thickness in spectral-domain optical coherence tomographyBRITISH JOURNAL OF OPHTHALMOLOGY
2023Neuro-Ophthalmic Adverse Events of COVID-21 Infection and Vaccines: A Nationwide Cohort Study INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
2022Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus TRANSLATIONAL VISION SCIENCE & TECHNOLOGY
2016Obstructive Sleep Apnea in Patients with Branch Retinal Vein Occlusion: A Preliminary Study Korean Journal of Ophthalmology
2015Ocular alignment after bilateral lateral rectus recession in exotropic children with cerebral palsyBRITISH JOURNAL OF OPHTHALMOLOGY
2015Ophthalmological manifestations in patients with Leigh syndromeBRITISH JOURNAL OF OPHTHALMOLOGY
2018Ophthalmoplegia in Mitochondrial Disease YONSEI MEDICAL JOURNAL
2016Optic Atrophy in a Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration.JOURNAL OF NEURO-OPHTHALMOLOGY
2021Optical Coherence Tomography Findings Facilitate the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Korean Journal of Ophthalmology
2020Population-based Incidence of Pediatric and Adult Optic Neuritis and the Risk of Multiple SclerosisOPHTHALMOLOGY
2022Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort GENES
2017Protective effects of biodegradable collagen implants on thinned sclera after strabismus surgery: a paired-eye studyJOURNAL OF AAPOS
2014Real stereopsis test using a three-dimensional display with Tridef software. YONSEI MEDICAL JOURNAL
2012Recurrent bilateral retinal vasculitis as a manifestation of post-streptococcal uveitis syndrome Korean Journal of Ophthalmology
2019Refractive Outcomes of 4-Year-old Children after Intravitreal Anti-vascular Endothelial Growth Factor versus Laser Photocoagulation for Retinopathy of Prematurity Korean Journal of Ophthalmology
2016Restoration of Retinally Induced Aniseikonia in Patients with Epiretinal Membrane after Early VitrectomyRETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
2016Retinal Artery Occlusion and the Risk of Stroke Development: Twelve-Year Nationwide Cohort StudySTROKE
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