5 hasil untuk "Anastasios Anastasakis"

Clinical and Spectral-Domain Optical Coherence Tomography Findings of Patients with Incomplete Visual Recovery after Anatomically Successful Retinal Detachment Surgery

Miltiadis K. Tsilimbaris; Aikaterini Chalkia; Chrysanthi Tsika dkk.

Journal of Ophthalmology, Vol. 2015 · 2015 · Inggris · DOAJ Scopus

Purpose. To identify causes of incomplete visual recovery in patients with anatomically successful retinal detachment surgery. Methods. This was a retrospective study of 61 eyes of 61 patients with at least 12-month follow-up and complete preoperative, intraoperative, and postoperative record…

Spontaneous Regression of Choroidal Neovascularization in a Patient with Pattern Dystrophy

Anastasios Anastasakis; Flamur Goleni; Gerasimos Livir-Rallatos dkk.

Case Reports in Ophthalmological Medicine, Vol. 2016 · 2016 · Inggris · DOAJ

Purpose. To present a case of a patient with pattern dystrophy (PD) associated choroidal neovascularization (CNV) that resolved spontaneously without treatment. Methods. A 69-year-old male patient was referred to our unit, for evaluation of a recent visual loss (metamorphopsias) in his left eye…

Nyctalopia during pregnancy due to vitamin A deficiency after bariatric sleeve gastrectomy: A case report

Eleftherios Anastasakis; Anastasios Anastasakis; Athina A. Samara dkk.

Clinical Case Reports, Vol. 12 No. 9 · 2024 · Inggris · DOAJ Dikeluarkan Scopus 2021

Key Clinical Message Herein, we report a rare case of nyctalopia diagnosed in the first trimester of pregnancy due to vitamin A deficiency as a result of a bariatric gastrectomy. Low serum vitamin A levels establish the diagnosis and the patient was treated with oral vitamin A supplements…

Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles

Smaragda, Kamakari; Vassiliki, Kokkinou; George, Koutsodontis dkk.

J Ophthalmol · 2018 · Inggris · PubMed Central

AIM: To evaluate the frequency and pattern of disease-associated mutations of ABCA4 gene among Greek patients with presumed Stargardt disease (STGD1). MATERIALS AND METHODS: A total of 59 patients were analyzed for ABCA4 mutations using the ABCR400 microarray and PCR-based sequencing of all coding…

Corrigendum to “Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles”

Smaragda Kamakari; Vassiliki Kokkinou; George Koutsodontis dkk.

Journal of Ophthalmology, Vol. 2018 · 2018 · Inggris · DOAJ Scopus