Hilal Eser-Ozturk,Ilknur Tugal-Tutkun
Hilal Eser-Ozturk
Behçet disease is a systemic vasculitis that can affect various organ systems. Ocular involvement is characterized by recurrent nongranulomatous panuveitis and retinal vasculitis attacks, followed by spontaneous remission periods. Recurren...
Opposing pathophysiological concepts in multiple evanescent white dot syndrome: The great MEWDS schism [0.03%]
多灶性蒸发性白点综合征的对立病理生理学概念：MEWDS的大分裂
Carl P Herbort Jr,Ioannis Papasavvas,Abdulrahman F Albloushi et al.
Carl P Herbort Jr et al.
Multiple evanescent white dot syndrome (MEWDS) is a benign posterior uveitis involving the outer retina-choriocapillaris complex. The clinical picture, since its first description in 1984, is well-established. Classified at the benign end o...
Normative values of accommodation functions in young Saudi adults in the Qassim region [0.03%]
沙特卡西姆地区年轻成人调节功能的正常值规范
Saif H Alrasheed,Muhammed S Alluwimi,Zoelfigar D Mohamed
Saif H Alrasheed
Purpose: The purpose is to establish normative values for accommodation functions in young adults in the Qassim Region of Saudi Arabia. Methods: ...
Is serum angiotensin-converting enzyme a suitable biomarker for differentiating idiopathic and demyelinating optic neuritis? [0.03%]
血清血管紧张素转换酶能否作为区分特发性和脱髓鞘视神经炎的生物标志物？
Alireza Dehghani,Nastaran-Sadat Hosseini,Majid Mirmohammadkhani et al.
Alireza Dehghani et al.
Purpose: The purpose of the study was to measure serum angiotensin-converting enzyme (ACE) in patients diagnosed with idiopathic and demyelinating optic neuritis (ON) as well as heathy individuals and assess its viability...
Behçet disease: A unique systemic vasculitis with a distinct form of ocular involvement [0.03%]
贝赫切特病：一种独特且具有特殊眼部受累形式的系统性血管炎
Ilknur Tugal-Tutkun,Ahmet Gül
Ilknur Tugal-Tutkun
Immunogenetics of Behçet's disease: Is there a link to recent phenotypic changes? [0.03%]
贝赫切特病的免疫遗传学：是否与近期表型变化有关？
Yohei Kirino,Masaki Takeuchi,Ahmet Gül
Yohei Kirino
Over the past decade, advances in genetic and genomic analyses, including genome-wide association studies, have provided substantial insights into the pathogenesis of Behçet's disease (BD). These studies revealed potential pathogenic mecha...
Clinical insights into mitochondrial retinopathy: A case report on m.3243A>G mutation and macular dystrophy [0.03%]
线粒体视网膜病的临床见解：m.3243A> G突变和黄斑营养不良病例报告
Nourelhouda Boussaid Othmani,Sebastian Mathew
Nourelhouda Boussaid Othmani
Mitochondrial disorders, particularly those associated with the m.3243A>G mutation in the MT-TL1 gene, can manifest with diverse systemic and ocular features, including mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-lik...
Advancements in keratoplasty: Exploring newer techniques and imaging modalities for enhanced surgical outcomes [0.03%]
角膜移植进展：探索新的技术及影像模式以增强手术效果
Sarita Aggarwal,Madhu Kumari,Nupur Bhatnagar
Sarita Aggarwal
Keratoplasty, the transplantation of corneal tissue, is a well-established surgical procedure for the treatment of various corneal diseases. Over the years, advancements in keratoplasty techniques have significantly improved surgical outcom...
Posterior scleritis in an 18-year-old female with primary familial brain calcification syndrome: Incidental finding or association? [0.03%]
18岁原发性家族性脑钙化综合征女患者的后巩膜炎：偶然发现还是相关联系？
Hala A Khalil,Khaled Helaiwa
Hala A Khalil
Primary familial brain calcification (PFBC) is an idiopathic neurological disease associated with intracranial calcification. An 18-year-old female, a known case of uncontrolled Type 1 diabetes mellitus, presented with unilateral progressiv...
Acceleration of moyamoya disease after anti-vascular endothelial growth factor intravitreal injections [0.03%]
眼内注射抗血管内皮生长因子药物加速 moyamoya 病发展
Abdulaziz K Alotaibi,Sameeha Fallatah,Nabeel Refka et al.
Abdulaziz K Alotaibi et al.
Moyamoya disease (MMD) is a rare, progressive, irreversible vaso-occlusive disease affecting the cerebral vasculature. The progressive occlusion of blood vessels leads to the development of collateral vessels to compensate for the insuffici...