Hou-bin Huang

Beijing, 100853, China

Last Updated: 09/26/2026

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Found 15 publications

Development of an Acute Intracranial Hypertension-Induced Rat Model for Terson Syndrome and Mechanisms of Blood-Retinal Barrier Breakdown.

Development of an Acute Intracranial Hypertension-Induced Rat Model for Terson Syndrome and Mechanisms of Blood-Retinal Barrier Breakdown.

Journal: Current eye research
Published: February 13, 2026

Nanosilver eye patch for ocular surface trauma: a prospective randomised trial and review of the literature.

Nanosilver eye patch for ocular surface trauma: a prospective randomised trial and review of the literature.

Journal: International journal of ophthalmology
Published: October 15, 2025

Impact of slanted lateral rectus recession on pediatric patients with convergence insufficiency intermittent exotropia.

Impact of slanted lateral rectus recession on pediatric patients with convergence insufficiency intermittent exotropia.

Journal: BMC ophthalmology
Published: May 16, 2025

Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families.

Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families.

Journal: Current medical science
Published: January 23, 2024

Retinal vessel density alteration after FS-LASIK for myopia with different axial lengths.

Retinal vessel density alteration after FS-LASIK for myopia with different axial lengths.

Journal: International journal of ophthalmology
Published: January 06, 2024

Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families.

Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families.

Journal: International journal of ophthalmology
Published: February 17, 2022

Novel mutations in the BEST1 gene cause distinct retinopathies in two Chinese families.

Novel mutations in the BEST1 gene cause distinct retinopathies in two Chinese families.

Journal: International journal of ophthalmology
Published: June 20, 2020

A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome.

A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome.

Journal: Experimental and therapeutic medicine
Published: November 18, 2018

Early Diagnosis of Recurrent Optic Neuritis Using Contrast-Enhanced T2 Fluid-attenuated Inversion Recovery Imaging: a Case Report.

Early Diagnosis of Recurrent Optic Neuritis Using Contrast-Enhanced T2 Fluid-attenuated Inversion Recovery Imaging: a Case Report.

Journal: Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih
Published: July 07, 2018

Recombination and identification of human alpha B-crystallin.

Recombination and identification of human alpha B-crystallin.

Journal: International journal of ophthalmology
Published: May 16, 2018

A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease.

A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease.

Journal: BMC medical genetics
Published: March 06, 2018

A new perspective for analyzing clinical characteristics of idiopathic retinal vasculitis, aneurysms, and neuroretinitis syndrome.

A new perspective for analyzing clinical characteristics of idiopathic retinal vasculitis, aneurysms, and neuroretinitis syndrome.

Journal: International ophthalmology
Published: December 09, 2017
Showing 1-12 of 15

Last Updated: 09/26/2026