Results 91 to 100 of about 1,171,218 (148)

Exfoliation Syndrome in Baja Verapaz Guatemala: A Cross-Sectional Study and Review of the Literature. [PDF]

J Clin Med, 2022
Paulson C, Thomas SC, Gonzalez O, Taylor S, Swiston C, Herrick JS, McCoy L, Curtin K, Chaya CJ, Stagg BC, Wirostko BM.   +10 more
europepmc   +1 more source

Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma

, 2009
Purpose: To investigate possible genetic associations of matrix metalloproteinase-1 (MMP1) and MMP3 gene polymorphisms with exfoliation syndrome (XFS) with (XFS/+G) and without (XFS/-G) glaucoma in a cohort of Greek patients.
Hadjigeorgiou, G. M., Almpanidou, P., Kotoula, M. G., Chatzoulis, D. Z., Pefkianaki, M., Dardiotis, E., Papathanasiou, A. A., Rodopoulou, P., Tsironi, E. E., Tsezou, A.   +9 more
core  

剥脱综合征性青光眼30例临床分析

Zhongguo shiyan zhenduanxue, 2012
剥脱综合征性青光眼（peseudo exfoliation glaucoma,PEG）也称剥脱性青光眼,是继发于剥脱综合征（exfoliation syndrome,ES）的一种青光眼类型。扩瞳后可见晶状体前囊表面沉着物的3个区[1-3]。本病无明显病因[4-9],多无自觉症状,发病时已出现明显视功能损害,目前疗效较差。现将我院2006年1月 ...
李丹, 李弘, 胥利平, 李秀昆
doaj  

Compositional Analysis of Extracellular Aggregates in the Eyes of Patients With Exfoliation Syndrome and Exfoliation Glaucoma. [PDF]

Invest Ophthalmol Vis Sci, 2021
De Maria A, Zientek KD, David LL, Wilmarth PA, Bhorade AM, Harocopos GJ, Huang AJW, Hong AR, Siegfried CJ, Tsai LM, Sheybani A, Bassnett S.   +11 more
europepmc   +1 more source

Summary of Utah Project on Exfoliation Syndrome (UPEXS): using a large database to identify systemic comorbidities. [PDF]

BMJ Open Ophthalmol, 2021
Pompoco CJ, Curtin K, Taylor S, Paulson C, Shumway C, Conley M, Barker DJ, Swiston C, Stagg B, Ritch R, Wirostko BM.   +10 more
europepmc   +1 more source

Novel method of assessing delamination of the anterior lens capsule using spectral-domain optical coherence tomography

Clinical Ophthalmology, 2012
Deborah KL Tan,1 Tin Aung,1–3 Shamira A Perera1,21Singapore National Eye Centre, Singapore; 2Singapore Eye Research Institute, Singapore; 3National University of Singapore, Yong Loo Lin School of Medicine, SingaporeBackground: Delamination of ...
Tan DKL, Aung T, Perera SA
doaj  

MSX1 Mutation in Witkop Syndrome; A Case Report

Iranian Journal of Medical Sciences, 2013
The Witkop syndrome is a rare autosomal dominant disorder characterized by the absence of several teeth and abnormalities of the nails. This is the first report of a rare genetic tooth and nail syndrome diagnosed in a 2.5-year-old boy with early ...
Faezeh Ghaderi, Somaye Hekmat, Reza Ghaderi, Majid Fardaei   +3 more
doaj  

Lysyl oxidase-like 1 polymorphisms in a southwestern Greek cataract population with pseudoexfoliation syndrome

Clinical Ophthalmology, 2016
Alexios A Panoutsopoulos,1 Vassiliki S Gartaganis,2 Marios P Giannakopoulos,1 Panos D Goumas,3 Evangelos D Anastassiou,4 Sotirios P Gartaganis1 1Department of Ophthalmology, School of Medicine, University of Patras, Achaia, Greece; 2Protein ...
Panoutsopoulos AA, Gartaganis VS, Giannakopoulos MP, Goumas PD, Anastassiou ED, Gartaganis SP   +5 more
doaj  

The cornea in exfoliation syndrome

, 1992
Exfoliation syndrome (EXS) is a disorder which affects some structures of the eye. We studied the changes of the cornea in patients with EXS and compared with those in normal persons.
Stefaniotou, M., Razis, N., Psilas, K., Kalogeropoulos, C.   +3 more
core  

Microvascular Changes in Exfoliation Syndrome: OCT Angiography Analysis of Peripapillary Density and Foveal Avascular Zone. [PDF]

J Ophthalmol
Karakiraz A, Bayraktar Ş.
europepmc   +1 more source