• Antenatal Findings of Keratitis-Ichthyosis-Deafness Syndrome
• Congenital aniridia in children
• Corneal Involvement in Wallenberg Syndrome: Case Report and Literature Review
• Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family
• First identification of ITM2B interactome in the human retina
• Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14
• Itpr1 regulates the formation of anterior eye segment tissues derived from neural crest cells
• Ligneous conjunctivitis in a Dandy-Walker syndrome: A rare case report
• National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician
• Novel mutation causing Zellweger syndrome
• Novel variants in CDH2 are associated with a new syndrome including Peters anomaly
• Ocular Findings in Pontine Tegmental Cap Dysplasia
• Ophthalmic Features of Spinocerebellar Ataxia Type 7: A Case Report
• Pseudonystagmus in progressive supranuclear palsy
• Teenager with a Unilateral Cloudy Eye
• Treatment of corneal neovascularization with topical aflibercept in a case of exposure keratopathy following cerebellar astrocytoma surgery