Results 121 to 130 of about 71,371 (303)
Iris metastasis of diffuse large B-cell lymphoma misdiagnosed as primary angle-closure glaucoma: A case report and review of the literature [PDF]
Li Jun +3 more
openalex +1 more source
Purpose Previous studies have shown that iris mechanical properties may play a role in the pathophysiology of primary angle-closure glaucoma (PACG).
Anup D. Pant +4 more
semanticscholar +1 more source
Abstract Aim To evaluate the impact of initial mono‐ versus multitherapy on the ocular surface and related quality of life after 5 years follow‐up in the Glaucoma Intensive Treatment Study (GITS). Method The study included patients with primary open‐angle glaucoma and pseudoexfoliation glaucoma who completed 5‐year follow‐up in GITS.
Gauti Jóhannesson +6 more
wiley +1 more source
Evolving concepts in angle closure and angle-closure glaucoma
Ma. Margarita Lat-Luna, MD
doaj
Clear lens extraction in angle-closure glaucoma patients
AIM: To describe the results of 5 consecutive cases of clear lens extraction in angle closure patients for the treatment of elevated intraocular pressure (IOP). METHODS: Retrospective observational case series.
Shan C. Lin +2 more
doaj +1 more source
Medication-induced acute angle closure attack [PDF]
OBJECTIVE: To review acute angle closure attacks induced by local and systemic medications. DATA SOURCES: PubMed literature searches up to August 2011. STUDY SELECTION: The following key words were used for the search: 'drug', 'iatrogenic', 'acute angle ...
Gangwani, RA, Lai, JSM
core
Cochrane Corner: evidence on the management of primary angle closure glaucoma [PDF]
Manuele Michelessi +2 more
openalex +1 more source
Primary angle closure and primary angle closure glaucoma in retinal vein occlusion
To investigate the frequency of primary angle closure (PAC) and primary angle closure glaucoma (PACG) in patients with retinal vein occlusion (RVO) based on a hospital population.
Ke Xu +4 more
semanticscholar +1 more source
A novel CPAMD8 nonsense mutation c.2679C>G (p.Tyr893*) was identified in a patient with congenital microcoria, leading to reduced mRNA expression and predicted protein truncation. ABSTRACT Congenital microcoria (MCOR) is a rare inherited ocular disorder. Here, we describe a novel nonsense variant in the CPAMD8 gene in a patient with MCOR.
Jing‐Fan Gao +4 more
wiley +1 more source

