Timing of macular hole surgery among vitreoretinal surgeons in the UK: A national survey, review of literature and future direction [0.03%]
Jonathan K Y Ng,Aimee Lloyd,Tsveta Ivanova et al.
Jonathan K Y Ng et al.
To survey current practice and opinion regarding the timing of idiopathic full thickness macular hole (iFTMH) surgery among consultant vitreoretinal surgeons in the United Kingdom (UK), and to provide an overview of the current literature a...
Early real-world outcomes of aflibercept 8 mg in previously treated neovascular age-related macular degeneration [0.03%]
Imran Karim Janmohamed,Havena Harahn,Barnaby Carr et al.
Imran Karim Janmohamed et al.
Background: Real-world evidence of aflibercept 8 mg in treatment-experienced patients remains limited. This study evaluated early outcomes of switching treatment-refractory patients with neovascular age-related macular de...
A child with Wyburn-Mason syndrome presented with bilateral but asymmetrical retinal arteriovenous malformations [0.03%]
Kou Liu,Xiaohan Yang,Chunli Chen
Kou Liu
Aaron Donnelly,Eoghan Culligan,Shane Whitlow
Aaron Donnelly
Yan Haihan,Jing Li,Jianmin Ma
Yan Haihan
Mohd Afzal,Sanjay Kumar Mishra,Khaleel M
Mohd Afzal
Ashish Markan,Piyush Adchitre,Pradeep Venkatesh
Ashish Markan
Boon Lin Teh,Stephen Winder
Boon Lin Teh
Secondary extraocular extension of choroidal melanoma following primary photodynamic therapy [0.03%]
Nadeem Atwan,Timothy Beckman,Hardeep S Mudhar et al.
Nadeem Atwan et al.
Background/objectives: Secondary extraocular extension (SEOE) following conservative treatment of choroidal melanoma (CM) is extremely rare, and its occurrence in patients treated with primary photodynamic therapy (PDT) h...
Retinopathy caused by a primary immune regulatory disorder - the spectrum of AIRE-associated retinopathy: case series and literature review [0.03%]
由主要免疫调节紊乱引起的视网膜病-AIRE相关视网膜病变的谱系：病例系列及文献回顾
Mohammad Anas,Andrew C Browning,Siying Lin et al.
Mohammad Anas et al.
Background/objective: Retinal involvement in autoimmune polyendocrine syndrome type 1 (APS1), a rare monogenic autoimmune disorder caused by mutations in the AIRE gene, is increasingly recognised but remains poorly define...