Hideki Chuman
Miyazaki, 8891692, Japan
Last Updated: 09/26/2026
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Found 29 publications
Correction to: Paired‑eye comparison of photocoagulation versus intravitreal bevacizumab for retinopathy of prematurity: long‑term visual, refractive, and ocular biometric outcomes at corrected ages 1, 5, and 9 years.
Journal: Japanese journal of ophthalmology
Published: July 29, 2026
Paired-eye comparison of photocoagulation versus intravitreal bevacizumab for retinopathy of prematurity: long-term visual, refractive, and ocular biometric outcomes at corrected ages 1, 5, and 9 years.
Journal: Japanese journal of ophthalmology
Published: January 23, 2026
Intravenous immunoglobulin for the acute treatment of refractory optic neuritis in Japan.
Journal: Japanese journal of ophthalmology
Published: December 23, 2024
Usage status of biologics for the chronic treatment of optic neuritis in neuromyelitis optica spectrum disorders in Japan.
Journal: Japanese journal of ophthalmology
Published: April 26, 2024
Assessing the Correlation Between Visual Acuity and Critical Fusion Frequency in Acute Optic Neuritis Before and After Steroid Therapy.
Journal: Cureus
Published: December 04, 2023
Evaluation of inner retinal function at different stages of primary open angle glaucoma using the photopic negative response (PhNR) measured by RETeval electroretinography.
Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
Published: April 05, 2023
Structure-function relationship between magnetic resonance imaging lesion areas and visual field defects in initial optic neuritis with altitudinal hemianopsia.
Journal: Japanese journal of ophthalmology
Published: December 09, 2022
Proposed System for Selection of Surgical Approaches for Craniopharyngiomas Based on the Optic Recess Displacement Pattern.
Journal: World neurosurgery
Published: November 22, 2022
Incidence of Leber hereditary optic neuropathy in 2019 in Japan: a second nationwide questionnaire survey.
Journal: Orphanet journal of rare diseases
Published: March 08, 2022
A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene.
Journal: American journal of ophthalmology case reports
Published: November 30, 2020
Last Updated: 09/26/2026