Structure-function relationship between handheld photopic negative response and macular GCIPL thickness in chronic optic neuropathy [0.03%]
慢性视神经病变患者手持式光感负反应与黄斑GCIPL厚度的结构功能关系研究
Yuri Seo,Dongheon Surl,Jinu Han
Yuri Seo
Purpose: To determine whether photopic negative response (PhNR) parameters obtained using a handheld electroretinography (ERG) device reflect quantitative indicators of residual retinal ganglion cell (RGC)-driven inner re...
Clinical course of a patient with PRSS56-associated nanophthalmos (isolated microphthalmia) and uveal effusion syndrome [0.03%]
PRSS56相关性纳米眼病（孤立性小眼球）和葡萄膜积液综合征的临床经过
Yukari Taguchi,Kazuki Kuniyoshi,Kei Mizobuchi et al.
Yukari Taguchi et al.
Purpose: To describe the detailed clinical course and genetic findings of a Japanese patient with nanophthalmos (isolated microphthalmia) who developed bilateral uveal effusion syndrome (UES). ...
Congenital grouped albinotic spots of the retinal pigment epithelium-a case report [0.03%]
先天性视网膜色素上皮层片状白化斑1例报告
Dhanashree Ratra,Devika Damle
Dhanashree Ratra
Purpose: To describe the clinical and multimodal imaging characteristics of congenital grouped albinotic spots (CGAS) and to explore their functional implications using full-field electroretinography (ERG). ...
Screening for RPE65 genetic variants in Egyptian children with inherited retinal disorders: a study from a tertiary eye care center in Egypt [0.03%]
埃及小儿遗传性视网膜病变患者RPE65基因变异筛查：来自埃及一家三级眼科护理中心的研究
Ayman Elghonemy,Mahmoud Y Issa,Tarek Saad Shoala et al.
Ayman Elghonemy et al.
Background: Pathogenic variants in the RPE65 gene cause various forms of inherited retinal dystrophies (IRD), which include Leber congenital amaurosis (LCA), early childhood-onset retinal dystrophy (ECORD), and various fo...
Serous Maculopathy due to Aspecific Choroidopathy (SMACH): a case report with differential diagnosis based on multimodal imaging analysis [0.03%]
基于多模态影像学分析的非特异性脉络膜病变所致浆液性黄斑病变（SMACH）1例报告及鉴别诊断
Xuan Ren,Xinxin Yu,Shuai Huang et al.
Xuan Ren et al.
Background: Serous Maculopathy Due to Aspecific Choroidopathy (SMACH) is a rare chorioretinal disease characterized by polymorphic, non-pigmented choroidal lesions, with or without subretinal fluid (SRF). Its clinical man...
Improvement of dynamic pupillary function after cataract surgery in eyes with pseudoexfoliation syndrome: a six-month longitudinal pupillometry study [0.03%]
pseudoexfoliation综合征患者白内障手术后动态瞳孔功能的改善：一项为期六个月的纵向瞳孔测量研究
Goksu Alacamlı,Omer Ozer,Murat Kasıkcı
Goksu Alacamlı
Purpose: Impaired pupillary dynamics are a well-recognized feature of pseudoexfoliation syndrome (PXF), yet little is known about how cataract surgery influences postoperative iris function in these eyes. This study aimed...
Impact of pupil dilation on IOL power calculation based on biometric measurements with Heidelberg Anterion [0.03%]
基于Heidelberg Anterion生物测量的瞳孔散大对IOL计算的影响研究
Sara Marquina-Martín,Francisco J Segura-Calvo,Martín Puzo-Bayod et al.
Sara Marquina-Martín et al.
Purpose: To evaluate the impact of pharmacologic pupil dilation (PD) on biometric measurements and intraocular lens (IOL) power calculation using different generation formulas in patients undergoing cataract surgery. ...
Enhancing the detection of visual-cognitive disruptions in automated dyslexia diagnosis using viscoelastic constitutive artificial neural networks for eye movement analysis [0.03%]
基于眼动分析的粘弹性本构人工神经网络在自动化阅读障碍诊断中提升视觉认知干扰检测能力的方法
S Regilan,R Indumathi,J Jenitha et al.
S Regilan et al.
Purpose: Dyslexia can be assessed using eye-tracking technology to monitor reading patterns, but challenges persist in distinguishing dyslexia-specific anomalies from those caused by other factors due to individual readin...
Multimodal neuro-ophthalmologic changes and the impact of CPAP therapy in severe obstructive sleep apnea: a prospective OCT, OCTA, and visual field study [0.03%]
多模式神经眼科改变及CPAP治疗在重度阻塞型睡眠呼吸暂停中的影响：一项前瞻性OCT、OCTA和视野研究
Yagmur Inalkac Gemici,Uzeyir Ozturk,Mustafa Erdogan et al.
Yagmur Inalkac Gemici et al.
Purpose: To evaluate structural, microvascular, and functional neuro-ophthalmologic changes in severe obstructive sleep apnea syndrome (OSAS) and to investigate the effects of 6-month continuous positive airway pressure (...
Blue cone monochromacy with parafoveal hyperautofluorescent ring caused by a novel OPN1LW p.Ile109Asn variant [0.03%]
由新型OPN1LW p.Ile109Asn变异引起的蓝色锥体单色视症伴旁中心局灶性高自身荧光环
Jessie Huang,Scott E Brodie,Jian Kong et al.
Jessie Huang et al.
Background: Blue Cone Monochromacy is a rare X-linked retinal disorder characterized by the selective loss of long-(L) and medium-(M) wavelength-sensitive cone function. While typically caused by large-scale genomic delet...