Results 101 to 110 of about 11,316 (195)

A cohort study of duplex Doppler examinations of the carotid artery in primary open angle glaucoma

open access: yes, 2014
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

open access: yes, 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.   +9 more
core  

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

open access: yes, 2011
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30例临床分析

open access: yesZhongguo 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  

Association between Obstructive Sleep Apnea and Exfoliation Syndrome: The Utah Project on Exfoliation Syndrome. [PDF]

open access: yesOphthalmol Glaucoma, 2021
Shumway C   +5 more
europepmc   +1 more source

Considerations on extracapsular cataract extraction and posterior chamber lens implantation in exfoliation syndrome

open access: yes, 1995
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

open access: yes, 2014
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

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