Results 31 to 40 of about 5,786 (184)

Axial length as a risk factor for pseudophakic rhegmatogenous retinal detachment: A Danish registry study

open access: yesActa Ophthalmologica, Volume 104, Issue 5, Page 517-525, August 2026.
Abstract Purpose To examine axial length as a risk factor for pseudophakic rhegmatogenous retinal detachment (pRRD). Methods We identified eyes that underwent phacoemulsification between 2 May 2002 and 10 November 2023 and had an axial length registered at the Departments of Ophthalmology in the Capital Region of Denmark or the private clinic ...
Ditte‐Marie Leegaard Holm   +7 more
wiley   +1 more source

Anterior segment alterations in congenital primary aphakia—a clinicopathologic report of five cases

open access: yesIndian Journal of Ophthalmology, 2020
Purpose: To report the clinicopathological features of corneal buttons in patients with congenital primary aphakia. Methods: Five corneal specimens of five patients with congenital primary aphakia who underwent penetrating keratoplasty (PKP) were studied
Sunita Chaurasia   +4 more
doaj   +1 more source

Current Landscape and Future Perspectives of Diabetic Retinopathy Therapy: Pharmacological Targets, Precision Laser Technology, and Clinical Evidence

open access: yesMedComm, Volume 7, Issue 7, July 2026.
Targeted biological agents targeting VEGF, integrin, dopamine D2 receptor, ROCK, and BCL‐XL have entered the clinical trial phase and deserve particular attention. The treatment paradigm has shifted toward personalized and precision medicine, positioning optimized SML as a promising adjunctive therapy.
Xinying Hu   +7 more
wiley   +1 more source

Gene Panel Analysis Reveals Overlapping Genetic Causes of Inherited Cataracts and Other Ocular Phenotypes in Bulgarian Patients

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.
We have identified 4 pathogenic/likely pathogenic changes and 2 variants of uncertain significance, 3 of which were novel. The identification of disease‐causing variants in the CRYAA, MYH9, RP2, and CLNC1 genes allowed us to establish an accurate genetic diagnosis of inherited cataract and to describe overlapping clinical phenotypes.
Kristiyana Vitanova   +10 more
wiley   +1 more source

Design of Experiments, Hirshfeld Surface Analysis, and Pharmacokinetics Predictions of Carbachol‐Loaded Solid Lipid Nanoparticles for Ocular Delivery

open access: yesChemistrySelect, Volume 11, Issue 28, 24 July 2026.
Schematic illustration of the carbachol (CCH)–solid lipid nanoparticles (SLN) formulation, highlighting its structural design of experiments (DoE), physicochemical characterization, Hirshfeld surface analysis and pharmacokinetics predictions. ABSTRACT Carbachol (CCH) is a potent acetylcholine receptor agonist of hydrophilic and charged nature, which ...
Valentina Paganini   +7 more
wiley   +1 more source

At‐home visual acuity in children using a custom iPhone application compared with standardized in‐office visual acuity testing

open access: yesOptometry and Vision Science, Volume 103, Issue 4, April 2026.
ABSTRACT Purpose To validate a custom smartphone application for at‐home visual acuity (VA) measurement in children. Methods A total of 452 children aged 3–17.5 years participated. Certified examiners measured in‐office test–retest VA (logMAR) using gold‐standard Amblyopia Treatment Study HOTV (3‐to‐6‐year‐olds, younger cohort) or electronic Early ...
Tawna L. Roberts   +29 more
wiley   +1 more source

Aniridia associated with congenital aphakia and secondary glaucoma

open access: yesIndian Journal of Ophthalmology, 2009
We report a case of aniridia associated with congenital aphakia and secondary glaucoma. A 35-year-old male presented with aniridia, congenital aphakia and secondary glaucoma in both eyes.
Moreker Mayur   +3 more
doaj  

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää   +14 more
wiley   +1 more source

Intraocular Lens Formula Comparison of Flanged Intrascleral Intraocular Lens Fixation with Double Needle Technique

open access: yesClinical Ophthalmology, 2023
Daniel S Malach,1 John Michael Guest,1 Christopher Adam,1 Jonah Joffe,2 Kim Le,2 Chaesik Kim,1 Xihui Lin1 1Kresge Eye Institute/Wayne State University Department of Ophthalmology, Detroit, MI, USA; 2Henry Ford Hospital Department of Ophthalmology ...
Malach DS   +6 more
doaj  

Effective Cataract Surgery Coverage and Potential Influencing Factors for Adults in Fujian, Southeast of China: Fujian Eye Study

open access: yesBioMed Research International, Volume 2026, Issue 1, 2026.
Purposes The purpose of this study is to identify the impact factors of effective cataract surgery coverage (eCSC) through a cross‐sectional epidemiological survey for the population in the southeast of China. Methods The eCSC for primary analysis was defined as the proportion of the population that underwent cataract surgery and achieved a good visual
Qinrui Hu   +8 more
wiley   +1 more source

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