6 results match your criteria: "Ophthalmica Institute of Ophthalmology and Microsurgery[Affiliation]"
Patient with recurrent mosaic KRAS variant: Rare oculoectodermal syndrome with severe neurologic phenotype.
J Dermatol
October 2022
1st Department of Pediatrics, Aristotle University of Thessaloniki, Hippokratio General Hospital Thessaloniki, Greece.
A Case of Early Keratoconus Associated with Eye Rubbing in a Young Child.
Ophthalmol Ther
September 2020
Ophthalmica Institute of Ophthalmology and Microsurgery, Thessaloniki, Greece.
Introduction: Keratoconus usually presents during puberty and is considered rare in young children.
Methods: Case report with clinical findings and computerized corneal tomography.
Results: We report the case of an 8-year-old girl with early bilateral keratoconus who presented with allergic conjunctivitis and persistent eye rubbing.
[Bilateral Linear Interstitial Keratitis in a Patient with Unilateral Recurrent Herpetic Keratitis].
Klin Monbl Augenheilkd
April 2020
Ophthalmica Institute of Ophthalmology and Microsurgery, Thessaloniki, Greece.
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".
J Ophthalmol
December 2018
Department of Ophthalmology, University of Crete School of Medicine, Heraklion, Greece.
[This corrects the article DOI: 10.1155/2018/5706142.].
View Article and Find Full Text PDFA Modified Surgical Technique to Treat Strabismus in Complete Sixth Nerve Palsy.
Ophthalmol Ther
December 2018
Ophthalmica' Institute of Ophthalmology and Microsurgery, Thessaloniki, Greece.
Introduction: A lot of different techniques have been proposed in order to manage abduction limitation secondary to sixth nerve palsy; however, anterior segment ischemia remains a concern. The aim of this study was to evaluate the results of augmented vertical recti muscle transposition (VRT) with partial recession of medial rectus muscle (MR) for complete, chronic sixth nerve palsy, a new modified technique that could also minimize the risk for anterior segment ischemia (ASI).
Methods: In this nonrandomized 8-year (2009-2017) retrospective review, 20 patients with complete sixth nerve palsy and contracted MR were enrolled.
Mutation Spectrum of the Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles.
J Ophthalmol
April 2018
Department of Ophthalmology, University of Crete School of Medicine, Heraklion, Greece.
Aim: To evaluate the frequency and pattern of disease-associated mutations of gene among Greek patients with presumed Stargardt disease (STGD1).
Materials And Methods: A total of 59 patients were analyzed for mutations using the ABCR400 microarray and PCR-based sequencing of all coding exons and flanking intronic regions. MLPA analysis as well as sequencing of two regions in introns 30 and 36 reported earlier to harbor deep intronic disease-associated variants was used in 4 selected cases.