Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Cemal Çavdarli"'
Publikováno v:
Therapeutic Advances in Ophthalmology, Vol 13 (2021)
Background and purpose: Randomised-controlled clinical trials (the ANCHOR and MARINA) examined the intravitreal anti-vascular endothelial growth factor (anti-VEGF) efficacy for eyes having fluorescein angiographic classic and occult (OCC) neovascular
Externí odkaz:
https://doaj.org/article/0f5a2ee352c74b7fafc5fd859263cb76
Publikováno v:
Guoji Yanke Zazhi, Vol 15, Iss 12, Pp 2040-2044 (2015)
AIM:To investigate the changes in intraocular pressure(IOP), central corneal thickness(CCT)and anterior chamber depth(ACD)in eyes with open angle glaucoma treated with topical latanoprost(0.005%, once a day)for 6mo.METHODS:Thirty seven eyes of 24 new
Externí odkaz:
https://doaj.org/article/bd7dcb1062794f1e895d280bcde9141e
Publikováno v:
Ahi Evran Medical Journal, Vol 5, Iss 1, Pp 28-32 (2021)
Purpose: The aim of this study is to compare the data obtained from two different optical coherence tomography (OCT) angiography devices. Materials and Methods: Thirty-three eyes of 18 patients without any systemic disorder who applied to our clinic
Externí odkaz:
https://doaj.org/article/9314fa31216449bbbd9b9d2b5695af6d
Publikováno v:
Guoji Yanke Zazhi, Vol 19, Iss 8, Pp 1276-1280 (2019)
AIM: To evaluate the real life anatomical and visual outcome after intravitreal anti-VEGF treatment in diabetic macular edema(DME)throughout 24mo. METHODS: Treatment naive central-involved DME patients with intraretinal and/or subretinal fluid and ba
Externí odkaz:
https://doaj.org/article/892ae3d962404e9a90eacc27a37913fe
Autor:
Cemal Çavdarli, Gönül Büyükyılmaz, Büşranur Çavdarlı, Sebile Çomçalı, Pınar Topçu Yılmaz, Mehmet Numan Alp
Background: Several structural, vascular density and perfusion studies were conducted in type 1 and 2 diabetes, even in the absence of retinopathy. The current study is the first to compare macular vessel densities (VD) by optical coherence tomograph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89359cfc7ab23b5d54d500f426bdd786
https://doi.org/10.21203/rs.3.rs-2495369/v1
https://doi.org/10.21203/rs.3.rs-2495369/v1
Publikováno v:
European Journal of Ophthalmology. 31:NP78-NP82
Introduction Iodine deficiency is a leading cause of preventable physical and mental retardation. Potassium iodate is used for iodine supplementation to prevent iodine deficiency. We herein report a case of toxic retinopathy following intentional ing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af4eb50838a6fb6cc1388e4d14d3375a
https://doi.org/10.1177/1120672120926862
https://doi.org/10.1177/1120672120926862
Publikováno v:
Arquivos Brasileiros de Oftalmologia, Vol 83, Iss 2, Pp 149-152 (2020)
Gyrate atrophy is a rare metabolic autosomal recessive disorder caused by ornithine aminotransferase enzyme deficiency that leads to characteristic progressive, degenerative chorioretinal findings. Patients complain mostly of low vision, night blindn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87325346691f3a0740157aff0534c0a8
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492020000200149&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492020000200149&tlng=en
Publikováno v:
Ahi Evran Medical Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46a5443fe7fcfb428ec84b9e7c43a554
https://doi.org/10.46332/aemj.847635
https://doi.org/10.46332/aemj.847635
Publikováno v:
Ophthalmic genetics. 41(6)
Objective: To determine the clinical relevance and frequency of BEST1 and PRPH2 mutations in a clinically diagnosed adult-onset vitelliform macular dystrophy (AVMD) group with Caucasian ethnicity. Methods: The study comprised 24 patients who had been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7346e363e47663d44f7d08fbde636ccd
https://pubmed.ncbi.nlm.nih.gov/32942919
https://pubmed.ncbi.nlm.nih.gov/32942919
Publikováno v:
Ophthalmic genetics. 41(3)
Familial Mediterranean fever (FMF) is a hereditary auto-inflammatory disease with accompanying findings of amyloidosis and vasculitis. M694V is one of the most common mutations associated with amyloidosis. This study compared the macular optical cohe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986bf18d80bd3bfd5ef853bf4bc2578a
https://pubmed.ncbi.nlm.nih.gov/32372681
https://pubmed.ncbi.nlm.nih.gov/32372681