Results 31 to 40 of about 907,150 (341)
Therapeutic Effect of Human Adipose Tissue-Derived Mesenchymal Stem Cells in Experimental Corneal Failure Due to Limbal Stem Cell Niche Damage [PDF]
, 2017 Producción CientíficaLimbal stem cells are responsible for the continuous renewal of the corneal epithelium. The destruction or dysfunction of these stem cells or their niche induces limbal stem cell deficiency (LSCD) leading to visual loss, chronic pain,
Calonge Cano, Margarita +7 more
core +2 more sources
Ocular Neurofibromatosis [PDF]
Cureus, 2021 A 14-year-old boy presented with a right orbital lid mass, which had slowly grown over the last 4.5 years, as well as some impaired visual acuity in the affected (right) eye. We assessed the patient by taking a detailed history and physical examination.
Alkhairy, Saba, Baig, Mahad M
openaire +2 more sources
Custom Ocular Prosthesis for Enucleated Eye: A Case Report
Journal of College of Medical Sciences-Nepal, 2016 The unfortunate loss or absence of an eye may be caused by a congenital defect, irreparable trauma, tumor, sympathetic ophthalmia, or the need for histologic confirmation of a suspected diagnosis.
Surya Narayan Pun +5 more
doaj +1 more source
Second primary malignancies after ocular adnexal lymphoma diagnosis
BMC Ophthalmology, 2021 Background Although studies have investigated the risk of second primary malignancies (SPMs) associated with lymphoma of various sites, limited studies have investigated this risk in patients with lymphoma originating within the ocular adnexa.
Asad Loya +3 more
doaj +1 more source
Frontiers in Microbiology, 2021 Coagulase-negative Staphylococcus (CoNS) is the most common pathogen causing traumatic endophthalmitis. Among which, Staphylococcus epidermidis is the most common species that colonizes human skin, eye surfaces, and nasal cavity.
Shudan Lin +12 more
doaj +1 more source
Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus [PDF]
, 2003 BACKGROUND: Leber’s congenital amaurosis (LCA) accounts for 5% of inherited retinal disease and is usually inherited as an autosomal recessive trait. Genetic and clinical heterogeneity exist.
Inglehearn, C.F. +5 more
core +1 more source
Surfactant protein D contributes to ocular defense against Pseudomonas aeruginosa in a murine model of dry eye disease. [PDF]
, 2013 Dry eye disease can cause ocular surface inflammation that disrupts the corneal epithelial barrier. While dry eye patients are known to have an increased risk of corneal infection, it is not known whether there is a direct causal relationship between ...
Evans, David +4 more
core +2 more sources
Extraocular Muscle Imbalance and Outcomes of Scleral Buckling Surgery for Primary Rhegmatogenous Retinal Detachment [PDF]
, 2020 Objective: The objective was to study the muscle imbalance, restrictive motility in unlike gazes and the outcomes of the scleral buckling surgery for rhegmatogenous retinal detachment.
Kawish, A. B. (Ayesha) +2 more
core +1 more source
COVID-19 Related Eye Manifestations: A Narrative Review
Journal of Pediatrics Review, 2022 Background: The COVID-19 pandemic has affected human beings in many ways. The presence of SARS-CoV-2 in conjunctival cells and its secretion has been reported in the literature.
Yousef Alizadeh +5 more
doaj
Journal of Research in Medical Sciences, 2017 The hyperimmunoglobulin E syndromes (HIESs) are very rare immunodeficiency syndromes with multisystem involvement, including immune system, skeleton, connective tissue, and dentition.
Hassan Hashemi +5 more
doaj +1 more source