Results 241 to 250 of about 1,887,887 (334)
Sirolimus in the Treatment of Vascular Anomalies
European journal of pediatric surgery, 2016 P. Triana +7 more
semanticscholar +1 more source
Paracetamol in Pregnancy: Reassurance Amidst Uncertainty
BJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
Athina Samara, Asma Khalil
wiley +1 more source
Optimizing Prolonged (6 h) Normothermic Machine Perfusion of Donor Kidneys (PROPER Study)
Artificial Organs, EarlyView.Prolonged ex situ normothermic machine perfusion of donor kidneys up to 6 h is feasible, maintaining viability and histological integrity. Key protocol optimizations include fresh red blood cells, albumin supplementation, and urine recirculation—laying the groundwork for assessment and potential pretransplant interventions in future clinical trials ...
Asel S. Arykbaeva +14 more
wiley +1 more source
Acta Ophthalmologica, EarlyView.Abstract Purpose To estimate the risk of rhegmatogenous retinal detachment (RRD) following pars plana vitrectomy (PPV) for full‐thickness macular hole (FTMH) or epiretinal membrane (ERM) in pseudophakic eyes. Methods We conducted a nationwide Danish registry‐based cohort study from 2010 to 2023.
Birgitte Romme Nielsen +6 more
wiley +1 more source
Nationwide trends in macular hole, epiretinal membrane and floaters surgery, 2010–2023
Acta Ophthalmologica, EarlyView.Abstract Purpose To examine the incidence of pars plana vitrectomy (PPV) for full‐thickness macular hole (FTMH), epiretinal membrane (ERM) and floaters over time and across regions in Denmark. Methods This nationwide registry‐based study included all patients undergoing PPV for FTMH, ERM, or floaters in Denmark from 2010 to 2023.
Birgitte Romme Nielsen +4 more
wiley +1 more source
Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care
Acta Ophthalmologica, EarlyView.Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Davide Romano +26 more
wiley +1 more source
Acta Ophthalmologica, EarlyView.Abstract Purpose To characterise the baseline clinical features and genotypes of adults with pre‐mRNA processing factor 31 (PRPF31)‐associated retinal dystrophy (RD) enrolled in a prospective, multicentre 4‐year natural history study, and to explore correlations between selected baseline parameters.
Kathrine Olaussen Eriksen +6 more
wiley +1 more source
Acta Ophthalmologica, EarlyView.Abstract Purpose To study ocular fundus morphology and its relation to growth in adolescents born moderate‐to‐late preterm (MLP) and full term. Methods This prospective and population‐based cohort study included 50 MLP adolescents (26 girls, mean age 16.5 years) and 50 full‐term controls (30 girls, mean age 16.7 years).
Alexandra Lind +6 more
wiley +1 more source
Vitreoretinal complications and surgical outcomes in patients with X‐linked retinoschisis
Acta Ophthalmologica, EarlyView.Abstract Purpose X‐linked retinoschisis (XLRS) is an inherited vitreoretinal disorder characterized by macular retinoschisis. In a subgroup of patients, peripheral retinoschisis can occur, potentially leading to complications such as vitreous haemorrhage (VH) and retinal detachment (RD).
Jonathan Hensman +11 more
wiley +1 more source
Acta Ophthalmologica, EarlyView.Abstract Congenital aniridia is a rare genetic disorder primarily caused by pathogenic variants of the PAX6 gene. It leads to various panocular anomalies, including aniridia‐associated keratopathy (AAK). This review highlights recent insights into its pathogenesis, focusing on clinical staging, microstructural changes in the cornea and molecular ...
N. Szentmáry +27 more
wiley +1 more source