Results 91 to 100 of about 29,301 (239)

Is Current Evidence Sufficient to Establish the Efficacy of Botulinum Toxin A in Treating Persistent Dry Eye Disease? A Systematic Review and Meta‐Analysis of Interventional Studies With a Critical Review Using GRADE Tool

open access: yesHealth Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Standard management of dry eye disease (DED) relies on artificial tears, anti‐inflammatory therapy, and punctal occlusion in selected cases. However, some patients continue to report persistent symptoms. The present article reviewed the efficacy of Botulinum Toxin A (BTX‐A) for DED that remained symptomatic after these ...
Mirsaeed Abdollahi   +6 more
wiley   +1 more source

Peculiarities of reaction to the eyelashes intrusion into the eye in case of penetrating ocular injury

open access: yesОфтальмохирургия, 2013
Purpose. To show the variations of eye reaction to the eyelashes intrusion into the eye in case of the penetrating ocular injury. Materials and methods.
T.A. Krasnovid, V.V. Vit, V.S. Aslanova
doaj  

The Hidden Danger in the Eyelids: Diagnosis and Treatment of Bilateral Phthiriasis Palpebrarum - A Rare Pediatric Case Report

open access: yesTürkiye Parazitoloji Dergisi
Phthiriasis palpebrarum is a rare infestation of the eyelids caused by Phthirus pubis. This condition is particularly noteworthy as it is a rare cause of red eyes in children and can often be confused with other forms of blepharoconjunctivitis.
Yusuf Samet Atlıhan   +4 more
doaj   +1 more source

Prevalence, Etiology, and Antifungal Resistance Profiles of Ocular Fungal Infections in Ghanaian Ophthalmic Patients: A Multicenter Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Ocular fungal infections are an important but often underrecognized cause of ocular morbidity, particularly in resource‐limited settings. Delayed diagnosis and inappropriate treatment can lead to poor visual outcomes and increased disease burden.
Isaiah Osei Duah Junior   +4 more
wiley   +1 more source

The Crescent Student Newspaper, January 20, 2006

open access: yes, 2006
Student newspaper of George Fox University.https://digitalcommons.georgefox.edu/the_crescent/2294/thumbnail ...
George Fox University Archives
core  

A Pilot Metagenomic Study Demonstrating Virtual Reality Head Mounted Displays Utilized in Medical Education Are Reservoirs of Viable Pathogenic Microbes

open access: yesMicrobiologyOpen, Volume 15, Issue 2, April 2026.
Metagenomic analysis identified 27 pathogenic bacteria including 4 "ESKAPE" pathogens (Enterobacter sp., Staphylococcus aureus, Klebsiella spp., and Escherichia coli) and numerous organisms associated with ocular infections. A broad range of antimicrobial resistance genes were identified conveying resistance to Methicillin, Aminoglycosides, Macrolides,
Adrian Goldsworthy   +8 more
wiley   +1 more source

The scum bag [PDF]

open access: yes, 2009
Novel for 14+ Self-conscious, studious Julia is bowled over by the arrival of Peter Groves, the Greek God, known to all his friends as Ami. He’s a real catch and Julia seems to be the one reeling him in.
James, G
core   +1 more source

Premixed Lidocaine With Fospropofol Disodium for Safety and Clinical Evaluation Regarding Paresthesia Upon Fospropofol Disodium Injection: A Preclinical Experimental Study and a Randomized Controlled Trial

open access: yesMedComm, Volume 7, Issue 4, April 2026.
This study explored the effect of lidocaine premixing on fospropofol‐induced paresthesia. While the mixture of fospropofol (FP) and lidocaine (LD) proved chemically stable and safe in preclinical tests, clinical results from randomized controlled trial showed no reduction in paresthesia in FP+LD group compared with FP+NS group.
Bo Jiao   +17 more
wiley   +1 more source

A Complex Neurodevelopmental Phenotype Resembling a Chromatinopathy With Concurrent 7p Duplication and 10p Deletion Involving ZMYND11: A Case Report and Literature Review

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 4, April 2026.
This study presents a 25‐year‐old female with global developmental delay, dysmorphic features, and a complex phenotype arising from co‐occurring chromosomal anomalies: a 6 Mb 10p15.3p14 microdeletion involving the ZMYND11 gene and a 7.6 Mb 7p22.3p21.3 microduplication.
Elia Marco Paolo Minale   +11 more
wiley   +1 more source

Novel Variants in KMT2C Further Support a Neurodevelopmental Disorder Distinct From Kleefstra and Kabuki Syndromes

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 4, April 2026.
Sedlackova et al. describe detailed phenotypes of three patients with novel variants in the KMT2C gene. After detailed phenotypic analysis, we found that our patients have phenotypes very similar to those previously described as KMT2C‐related Kleefstra syndrome 2, and thus further extend the list of KMT2C causal variants.
Lucie Sedláčková   +3 more
wiley   +1 more source

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