Results 101 to 110 of about 11,316 (195)
DNA Polymorphism of the LOXL1 Promoter Region in Exfoliation Syndrome in Uygur Individuals in XinJiang, China. [PDF]
Ma Y, Yang M, Chen X, Yi X.
europepmc +1 more source
A cohort study of duplex Doppler examinations of the carotid artery in primary open angle glaucoma
Objectives To explore the possibility of pathological change in the common carotid artery at the bifurcation and in the internal carotid artery beyond the bifurcation which could contribute to a reduced diastolic pressure as observed in primary open ...
Aldoori, M. I. +6 more
core +1 more source
Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma
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. +9 more
core
Cytokine and Growth Factor Analysis in Exfoliation Syndrome and Glaucoma. [PDF]
Park DY, Kim M, Cha SC.
europepmc +1 more source
Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma
Purpose: To investigate possible genetic association of matrix metalloproteinase-1 (MMP1) and matrix metalloproteinase-3 (MMP3) gene polymorphisms with exfoliation syndrome (XFS) with (XFS/+G) and without glaucoma (XFS/-G) in a cohort of Greek patients ...
Πευκιανάκη, Μαρία +1 more
core +1 more source
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
Association between Obstructive Sleep Apnea and Exfoliation Syndrome: The Utah Project on Exfoliation Syndrome. [PDF]
Shumway C +5 more
europepmc +1 more source
Bu çalışmada katarakt ameliyatı olan olgularda eksfoliasyon send¬romunun prevalansı ve klinik özellikleri değerlendirilerek-ameliyat sırası ve sonrası komplikasyonlannın eksfoliasyonsuz gözlere göre karşılaştırılması yapıldı.
Cenap Güler +3 more
core
Comèl-Netherton syndrome – case report
Introduction. Comèl-Netherton syndrome is a rare autosomal recessive genodermatosis characterized by congenital ichthyosiform erythroderma, ichthyosis linearis circumflexa, trichorrhexis invaginata, and atopic diathesis.
Izabela Błażewicz +3 more
core +1 more source
Exfoliation Syndrome in Egypt: Prevalence and Association with Cataract in a Large Cohort. [PDF]
Aziz BF +3 more
europepmc +1 more source

