A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. [PDF]
, 2017 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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Ocular circulatory changes following scleral buckling procedures. [PDF]
, 1992 Akitoshi Yoshida +3 more
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Clinical Ophthalmology, 2020 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
Prophylactic scleral buckle for prevention of retinal detachment following vitrectomy for macular hole [PDF]
, 2000 Robert E. Morris
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A matched study of primary scleral buckle placement during repair of posterior segment open globe injuries [PDF]
, 2002 Jorge G. Arroyo
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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]
, 2005 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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Vitrectomy and gas for inferior break retinal detachments: are the results comparable to vitrectomy, gas, and scleral buckle? [PDF]
, 2004 Louisa Wickham
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Modified self sealing sclerotomy for drainage of subretinal fluid during scleral buckling surgery [PDF]
, 2004 Julio Yepez +3 more
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