Results 1 to 10 of about 95,483 (206)
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
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Seven-year follow-up of posterior chamber phakic intraocular lens with central port design
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
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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
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
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]
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
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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
Optical coherence tomography (OCT) is a noninvasive imaging technique used to qualitatively and quantitatively analyze various layers of the retina.
Cody Lo +2 more
doaj +1 more source
Genetic analysis for two italian siblings with usher syndrome and schizophrenia. [PDF]
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
ObjectivePrevious studies have demonstrated altered brain activity in strabismic amblyopia (SA). In this study, low-frequency repetitive transcranial magnetic stimulation (rTMS) was applied in children with strabismic amblyopia after they had undergone ...
Yi-Ning Wang +7 more
doaj +1 more source
Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene. [PDF]
Occult macular dystrophy (OMD) is an inherited macular disease characterized by progressive visual decline with the absence of visible retinal abnormalities. Typical alterations of the retinal structure are detectable by spectral domain optical coherence
Colavito, Davide +4 more
core +1 more source

