Results 141 to 150 of about 682,435 (246)

2015-2016 Pediatric Subspecialty Trainees

, 2016
Photo composite of the graduate pediatric trainees in allergy/immunology, child abuse pediatrics, child neurology, clinical child psychology, clinical cytogenetics, clinical pharmacology, developmental-behavioral pediatrics, neonatal-perinatal medicine ...
Children\u27s Mercy Hospital
core   +1 more source

A Bibliometric Analysis of Social Perception and Academic Trends on Gender and Race in Ophthalmology

Background: Gender and race disparities in ophthalmology have gained increased attention in recent years due to their clinical and societal significance.
Nguyen, Helen N, Choudhry, Hassaam S, Kaleem, Mona A, Dossantos, Jason, Shukla, Aakriti G, Kumarapuram, Siddhant, Choudhry, Hannaan S, Elam, Angela   +7 more
core   +1 more source

Interpreting the structure–function relationship in high myopia‐associated glaucoma: A review

Acta Ophthalmologica, EarlyView.
Abstract Visual field (VF) interpretation in high myopia‐associated glaucoma (HMG) is challenging due to frequent structure–function discordance and coexisting myopia‐related changes. These changes may reduce the reliability of conventional structure–function mapping and increase the risk of misclassifying non‐glaucomatous VF abnormalities as ...
Ruby S. Chan, Ya Xing Wang, Jin Wook Jeoung, Jost B. Jonas, Minxin Liu, Ching‐Yu Cheng, Rachel S. Chong   +6 more
wiley   +1 more source

Inter‐observer variability is unlikely to explain regional differences in retinopathy of prematurity in Norway

Acta Ophthalmologica, EarlyView.
Abstract Purpose To test inter‐observer variation of plus disease diagnoses among Norwegian ophthalmologists and treatment centres. Methods All ophthalmologists in Norway who make individual retinopathy of prematurity (ROP) treatment decisions were invited to grade retinal images using a web‐based image grading platform.
Dordi Austeng, Kyrre Moljord, Tora Sund Morken, Aaron S. Coyner, J. Peter Campbell   +4 more
wiley   +1 more source

Uncorrected Refractive Errors Among Children Attending Pediatric Ophthalmology Clinic at Security Forces Hospital, Makkah, Saudi Arabia. [PDF]

Cureus, 2023
Khouj G, Alharbi A, Alghamdi W, Alzahrani Y, Fallata A.   +4 more
europepmc   +1 more source

Ophthalmologic Complications in NF1 Patients Treated with MEK Inhibitors

MEK inhibitors are novel, promising therapies for Neurofibromatosis type 1 (NF1) manifestations including optic gliomas. Due to known potential ophthalmic side effects, such as MEKi associated retinopathy (MEKAR), patients undergoing MEKi treatment ...
May Ameri; Lena Hummel; Shaikha AlQahtani; Zsila Sadighi; Nagham Al-Zubidi
core  

Radial outer retina reflectivity (RORR) sign in LAMP2‐associated retinopathy

Acta Ophthalmologica, EarlyView.
Abstract Purpose To describe the radial outer retina reflectivity (RORR) sign in patients carrying pathogenic variants in the X‐linked lysosome‐associated membrane protein‐2 (LAMP2) gene and to review the histologic characteristics of LAMP2 expression in the human retina.
Rachael C. Heath Jeffery, Bohdan Kousal, Ulrike Grünert, Christine A. Curcio, Svetlana Cherepanoff, Tina M. Lamey, Michel Michaelides, Chrysanthi Tsika, Isabelle Chow, Omar A. Mahroo, Seungmin Lee, Martin Meliska, Milos Kubanek, Jakub Sikora, Siying Lin, Raymond C. B. Wong, Petra Liskova, Fred K. Chen   +17 more
wiley   +1 more source

Large Language Model-Generated Patient Education Materials in Pediatric Ophthalmology: A Scoping Review. [PDF]

Clin Ophthalmol
Mohamed AA, Armstrong TS, Srivastava O, Ing E, Pollock T, Solarte C.   +5 more
europepmc   +1 more source

Eye disorders spectrum: a tertiary hospital pediatric ophthalmology clinic based in Ethiopia. [PDF]

BMC Ophthalmol, 2022
Kidane YT, Teshome AW.
europepmc   +1 more source

Clinical manifestations of dual‐gene variants in retinitis pigmentosa

Acta Ophthalmologica, EarlyView.
Abstract Purpose Retinitis pigmentosa (RP) is an inherited retinal disease (IRD), whereby each affected individual typically harbours pathogenic variants in a single causative gene, yet the disorder exhibits marked genetic heterogeneity, with more than 100 genes reported to underlie RP.
Lasse Wolfram, Jan‐Philipp Bodenbender, David A. Merle, Milda Reith, Anton Sonntag, Krunoslav Stingl, Tobias B. Haack, Theresia Zuleger, Bernd Wissinger, Laura Kühlewein, Katarina Stingl, Susanne Kohl   +11 more
wiley   +1 more source