Results 261 to 270 of about 131,981 (335)

A Rare Combination of Genitourinary Vascular Anomaly

, 2018
Rohini Arathala, Vishwajit Deshmukh, Satish Subbiah Nagaraj, Hemanth Kommoru, K Ariyanachi   +4 more
openalex   +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, Martin Nissen Hermann, Jakob Grauslund, Morten la Cour, Mark Alberti   +4 more
wiley   +1 more source

Electrophysiological monitoring of the nonrecurrent inferior laryngeal nerve and radiological evaluation of concurrent vascular anomalies. [PDF]

Front Endocrinol (Lausanne)
Sormaz IC, Iscan AY, Tunca F, Kostek M, Aygun N, Matlim Ozel T, Soytas Y, Poyanli A, Sari S, Uludag M, Giles Senyurek Y.   +10 more
europepmc   +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, Vito Romano, Alejandra Daruich, Giulio Ferrari, Matthieu Robert, Francesco Semeraro, Neil Lagali, Dominique Bremond‐Gignac, the ANIRIDIA‐NET Clinical Guidelines Working Group, Miriam Barbany, Claus Cursiefen, Stefano Ferrari, Francisco Figueiredo, Christina Grupcheva, Jesper Hjortdal, Elke Kreps, Erlend Landsend, Laura Mauring, Hilde Pedersen, Nora Szentmáry, Bogumil Wowra, the Aniridia‐Europa and Geniris Working Group, Sophie Valleix, Juan Álvarez de Toledo, James Lauderdale, Tor Paaske Utheim, Paolo Rama   +26 more
wiley   +1 more source

Challenges in Management of the Adult Vascular Anomalies Population: A Case Report and Review of the Literature. [PDF]

Semin Intervent Radiol
Strain D, Nelson KJ.
europepmc   +1 more source

Characterising PRPF31‐associated retinal dystrophy: Clinical insights from baseline data in a natural history study

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, Jon Roger Eidet, Ulrika Kjellström, Jacopo Baldesi, Ragnheidur Bragadóttir, Leonardo Colombo, Josephine Prener Holtan   +6 more
wiley   +1 more source

Exploring ocular fundus morphology in relation to growth in adolescents born moderate‐to‐late preterm

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, Sara Ali, Titus Ovik, Zoran Popovic, Eva Aring, Jovanna Dahlgren, Marita Andersson Grönlund   +6 more
wiley   +1 more source

Cryogun cryotherapy for the management of a large benign oral vascular anomaly - A case report

Shih-Wen Chu, Meng-Ling Chiang, Jyh‐Kwei Chen   +2 more
openalex   +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, Leo C. Hahn, Mary J. van Schooneveld, Roselie M. H. Diederen, Filip van den Broeck, Jacoline B. Ten Brink, Alberta A. Thiadens, Maria M. van Genderen, L. Ingeborgh van den Born, Bart P. Leroy, Carel B. Hoyng, Camiel J. F. Boon   +11 more
wiley   +1 more source

Correction to: Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA. [PDF]

Orphanet J Rare Dis
Revencu N, Eijkelenboom A, Bracquemart C, Alhopuro P, Armstrong J, Baselga E, Cesario C, Dentici ML, Eyries M, Frisk S, Karstensen HG, Gene-Olaciregui N, Kivirikko S, Lavarino C, Mero IL, Michiels R, Pisaneschi E, Schönewolf-Greulich B, Wieland I, Zenker M, Vikkula M.   +20 more
europepmc   +1 more source