Results 111 to 120 of about 7,469 (243)
Nami Nishikiori, Hiroshi OhguroDepartment of Ophthalmology, Sapporo Medical University School of MedicineBackground: Scleral buckling is still a common procedure to repair rhematogenous retinal detachment, and acute or chronic infection of the scleral ...
Nami Nishikiori, Hiroshi Ohguro
doaj
Arterial occlusion after scleral buckling
We present a report of a young man with bilateral retinal dialyses in whom surgery, in the form of scleral buckling, was initially performed only to one eye. Post-operatively, he developed features of combined central retinal and distal choroidal artery occlusions in the operated eye.
Aslam, SA +3 more
openaire +3 more sources
Nicolas A Yannuzzi, Nimesh A Patel, Audina M Berrocal, Jayanth Sridhar Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USACorrespondence: Jayanth SridharDepartment of Ophthalmology,
Yannuzzi NA +3 more
doaj
Finite Element Modelling of Soft Contact Lenses on Eye [PDF]
When fitting soft contact lenses, it is impossible to visualise the tear layer below the lens in white light. In addition, being permeable, soft lenses absorbs normal fluorescein and use of high molecular fluorescein is not sensitive enough to identify ...
Abass, AMFF +4 more
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Retinectomy vs vitrectomy combined with scleral buckling in repair of posterior segment open-globe injuries with retinal incarceration [PDF]
Yong Wei +4 more
openalex +1 more source
Pars plana vitrectomy for primary rhegmatogenous retinal detachment
Stephen G Schwartz, Harry W Flynn JrDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USAAbstract: Pars plana vitrectomy (PPV) is growing in popularity for the treatment of primary ...
Stephen G Schwartz, Harry W Flynn Jr
doaj
Eye Biometry Shift after Scleral Buckling Procedure
А. Н. Куликов +2 more
openalex +2 more sources
A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. [PDF]
Marfan syndrome is a pleiotropic connective tissue disease inherited as an autosomal dominant trait, mostly caused by mutations in the FBN1 gene, which is located on chromosome 15q21.1 and encoding fibrillin 1.
Bellacchio, Emanuele +11 more
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بررسی شيوع و عوامل خطرساز خونريزی فوق مشيميهای ناشی از عمل جراحی اسکلرال باکلينگ جهت درمان دکولمان رگماتوژن در مجتمع رسول اکرم(ص) در سالهای 77- 1368 [PDF]
خونريزی فوق مشيميهای از عوارض جدی جراحیهای داخل چشمی از جمله اسکلرال باکلينگ است که اثرات زيادی بر نتيجه جراحی و سرانجام بينايی بيمار دارد. هدف از اين مطالعه تعيين شيوع خونريزی فوق مشيميهای حين عمل اسکلرال باکلينگ و عوامل خطر بروز آن در مجتمع رسول ...
الماسی, مریم +4 more
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Presumed Sympathetic Ophthalmia After Scleral Buckling Surgery: Case Report [PDF]
Seyedeh Maryam Hosseini +4 more
openalex +1 more source

