Results 101 to 110 of about 25,200 (252)

INFLUENCE OF OPTIC NERVE DRUSEN ON VISUAL FUNCTIONS IN CHILDREN AND ADOLESCENTS WITH ESSENTIAL ARTERIAL HYPERTENSION

Acta Biomedica Scientifica, 2016
The article presents data examination of children and male adolescents, aged 8 to 17 years without eye pathologies, with primary hypertension diagnosis - established at the clinic of Scientific Centre for Family Health and Human Reproduction Problems ...
A. G. Shchuko, T. N. Lureva, Y. N. Savina, D. Y. Samsonov   +3 more
doaj   +1 more source

Angioid streaks and optic disc drusen in cherubism: a case report

, 2021
Luiz Guilherme Marchesi Mello, Fábio Petersen Saraiva, Mário Luiz Ribeiro Monteiro   +2 more
openalex   +1 more source

Using Directional OCT To Analyze Photoreceptor Visibility Over AMD-Related Drusen [PDF]

, 2022
Brennan Marsh-Armstrong, Kelly S. Murrell, Denise Valente, Ravi S. Jonnal   +3 more
openalex   +1 more source

Subthreshold Nanosecond Laser, from Trials to Real-Life Clinical Practice: A Cohort Study

Clinical Ophthalmology, 2021
Hasan Chichan,1,2 Matthias Maus,2,* Ludwig M Heindl1,3,* 1Department of Ophthalmology, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, 50923, Germany; 2Sehkraft Eye Center, Cologne, 50667, Germany; 3Center for ...
Chichan H, Maus M, Heindl LM
doaj  

Association of Optic Nerve Head Drusen with Best Vitelliform Macular Dystrophy: A Case Series

Case Reports in Ophthalmology, 2018
Purpose: To report the association of optic nerve head (ONH) drusen with Best vitelliform macular dystrophy (BVMD). Methods: Chart review. Patients: Five patients from 3 families.
Robert J. White, Daniel J. Watson, Dara D. Koozekanani, Sandra R. Montezuma   +3 more
doaj   +1 more source

Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers. [PDF]

, 2016
PurposeWe determined the phenotypic variation, disease progression, and potential modifiers of autosomal dominant retinal dystrophies caused by a splice site founder mutation, c.828+3A>T, in the PRPH2 gene.MethodsA total of 62 individuals (19 families)
Birch, David G, Bowne, Sara J, Conneely, Karen N, Daiger, Stephen P, Hughbanks-Wheaton, Dianna K, Shankar, Suma P, Stone, Edwin M, Sullivan, Lori S   +7 more
core  

Spectral-Domain and Swept-Source OCT Angiographic Scans Yield Similar Drusen Measurements When Processed with the Same Algorithm

Ophthalmology Science
Purpose: An algorithm developed to obtain drusen area and volume measurements using swept-source OCT angiography (SS-OCTA) scans was tested on spectral-domain OCT angiography (SD-OCTA) scans. Design: Retrospective study.
Farhan E. Hiya, MD, Jeremy Y. Liu, MD, Mengxi Shen, MD, Gissel Herrera, MD, Jianqing Li, MD, Qinqin Zhang, PhD, Luis de Sisternes, PhD, Robert C. O'Brien, PhD, Philip J. Rosenfeld, PhD, MD, Giovanni Gregori, PhD   +9 more
doaj   +1 more source

Comment on “Drusen and pachydrusen: the definition, pathogenesis, and clinical significance” [PDF]

, 2021
Jay Sheth
openalex   +1 more source

Peptide redesign for inhibition of the complement system: Targeting age-related macular degeneration. [PDF]

, 2016
PurposeTo redesign a complement-inhibiting peptide with the potential to become a therapeutic for dry and wet age-related macular degeneration (AMD).MethodsWe present a new potent peptide (Peptide 2) of the compstatin family.
Cabrera, Andrea P, Ghosh, Kaustabh, Gorham, Ronald D, Harrison, Reed ES, Johnson, Lincoln V, Mohan, Rohith R, Morikis, Dimitrios   +6 more
core   +1 more source

Expanding the Interface: Overlooked Dermatologic Disorders With Ocular Involvement

JEADV Clinical Practice, Volume 4, Issue 5, Page 1239-1243, December 2025.
A George
wiley   +1 more source