Results 1 to 10 of about 94,750 (283)

A Clinical Case of Successful Penetrating Keratoplasty after Corneal Perforation that Occurred against the Background of Dacryoadenitis

open access: yesOftalʹmologiâ, 2023
The article presents a clinical case of penetrating keratoplasty performed in a patient after corneal perforation against the background of dacryoadenitis.
G. Sh. Arzhimatova   +4 more
doaj   +1 more source

Seven-year follow-up of posterior chamber phakic intraocular lens with central port design

open access: yesEye and Vision, 2021
Background To assess the clinical outcomes of the Visian Implantable Collamer Lens (ICL) with a central port throughout 7 years of follow-up. Methods Eighty-four eyes of 52 patients were evaluated over a follow-up period of 7 years after V4c ICL ...
Luis Fernández-Vega-Cueto   +4 more
doaj   +1 more source

Evaluation of Blood Flow Parameters of the Macular Area and Optic Disc in Patients with Combination of Glaucoma and Axial Myopia

open access: yesOftalʹmologiâ, 2022
Purpose. To analyze the indicators of blood flow in the macular region and the peripapillary region in patients with a combination of glaucoma and axial myopia.Patients and methods. The paper analyzes the results of a study of 186 patients (343 eyes): 51
E. N. Eskina   +4 more
doaj   +1 more source

Predictability of the Refractive Effect after Laser Correction. Determining Factors. Review

open access: yesOftalʹmologiâ, 2023
Currently, refractive surgery using modern laser systems for the correction of various types of ametropia is one of the most widespread and performed operations worldwide.
E. N. Eskina   +3 more
doaj   +1 more source

Inadvertent trypan blue staining of posterior capsule during cataract surgery associated with Argentinian flag event [PDF]

open access: yes, 2016
Trypan blue is common in visualizing the anterior capsule during cataract surgery. Inadvertent staining of the posterior capsule during phacoemulsification is a rare complication and there are few reports in the literature.
Alapati, Neeti M   +3 more
core   +8 more sources

Retrospective Analysis of the Results and Causes of Penetrating Keratoplasty with Native Donor Material in a Multidisciplinary Hospital (Along the Example of MCOC Botkin Hospital)

open access: yesOftalʹmologiâ, 2023
Penetrating keratoplasty (PC) is an operation of choice for urgent and planned conditions of the pathologic cornea. Moscow City Ophthalmological  Center “Botkin Hospital” together with the Moscow Coordination Center for  Organ Donation) over the past ...
G. Sh. Arzhimatova   +3 more
doaj   +1 more source

Ocular Refraction at Birth and Its Development During the First Year of Life in a Large Cohort of Babies in a Single Center in Northern Italy [PDF]

open access: yes, 2020
The purpose of this study was to investigate refraction at birth and during the first year of life in a large cohort of babies born in a single center in Northern Italy.
Bartollino S.   +7 more
core   +1 more source

Three-year follow-up of posterior chamber phakic intraocular lens with a central port design after deep anterior lamellar keratoplasty

open access: yesEye and Vision, 2022
Background To evaluate clinical outcomes of the Visian implantable collamer lens (ICL) with a central port to correct myopia and astigmatism after deep anterior lamellar keratoplasty (DALK) for keratoconus throughout 3 years of follow-up.
Belén Alfonso-Bartolozzi   +5 more
doaj   +1 more source

Genetic analysis for two italian siblings with usher syndrome and schizophrenia. [PDF]

open access: yes, 2012
Usher syndrome is a group of autosomal recessive genetic disorders characterized by deafness, retinitis pigmentosa, and sometimes vestibular areflexia.
Article Id   +5 more
core   +3 more sources

Rare diseases leading to childhood Glaucoma. epidemiology, pathophysiogenesis, and management [PDF]

open access: yes, 2015
Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of
Abdolrahimzadeh, Solmaz   +5 more
core   +10 more sources

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