Results 91 to 100 of about 3,035 (199)

Clinical Observation of Posterior‐Chamber Phakic Implantable Collamer Lens V4c Implantation in Myopic Patients with Shallow Anterior Chamber Depth: A Retrospective, Consecutive Observational Study

open access: yesJournal of Ophthalmology, Volume 2024, Issue 1, 2024.
Purpose. The reference range for the preoperative anterior chamber angle width for ICL surgery is unclear. Our objective was to assess the clinical effect and the range of anterior chamber angle width of posterior‐chamber implantable collamer lens V4c (ICL V4c) implantation in patients with anterior chamber depth (ACD) < 2.8 mm. Methods.
Juan Yuan   +6 more
wiley   +1 more source

Deep capillary retinal ischemia and high-titer prothrombin-associated antiphospholipid antibodies: A case series of three patients

open access: yesAmerican Journal of Ophthalmology Case Reports, 2019
Purpose: Acute macular neuroretinopathy has been shown to be due to ischemia of the deep capillary retinal plexus and most cases occur in young women; we hypothesized that there may be an association with antiphospholipid antibodies.
Jill R. Schofield   +3 more
doaj   +1 more source

Paracentral homonymous hemianopic scotoma caused by anterior choroidal artery infarction [PDF]

open access: yesQJM: An International Journal of Medicine, 2021
A Mitsutake   +4 more
openaire   +2 more sources

Ceeable Visual Field Analyzer (CVFA^(TM) for the Portable, Comprehensive, and Tele-medical Assessment of Visual Performance over Time in Warfighters, Pilots, Veterans, and Civilians [PDF]

open access: yes, 2016
We introduce a portable, easy-to-use, worldwide accessible (i.e., web-based), and comprehensive tele-medical visual performance assessment system – the Ceeable Visual Field Analyzer (CVFATM) – for warfighters, pilots, veterans, and civilians to: (1 ...
Adams, Chris   +2 more
core   +1 more source

Retinal Ischemia as a Presenting Ocular Sign of Neurofibromatosis Type 2

open access: yesCase Reports in Ophthalmological Medicine, Volume 2024, Issue 1, 2024.
Purpose. Specific retinal abnormalities of neurofibromatosis type 2 (NF2) commonly include retinal astrocytoma and combined hamartoma of the retina and retinal pigment epithelium. Vasculopathy is an uncommon manifestation of NF2. We reported an NF2 patient presenting with retinal ischemia. Observations.
Binbin Zhao   +2 more
wiley   +1 more source

Paracentral acute middle maculopathy after uneventful ocular surgery with local anaesthetic blocks [PDF]

open access: yes, 2021
OBJECTIVE: To describe the role of local anaesthetic blocks as a potential cause of paracentral acute middle maculopathy (PAMM) after uneventful ocular surgery. METHODS: Retrospective, observational, international, multicentre case series.
Adán, A   +7 more
core  

A Case of Overlapping Choriocapillaritis Syndromes: Multimodal Imaging Appraisal

open access: yesJournal of Ophthalmic & Vision Research, 2012
Purpose: To present a patient with overlapping choriocapillaritis syndromes who first presented as a typical case of multiple evanescent white dot syndrome (MEWDS) and later with characteristic findings compatible with multifocal choroiditis (MFC). Case
Tatiana Kuznetcova   +2 more
doaj  

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]

open access: yes, 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   +7 more
core  

Reorganization of retinotopic maps after occipital lobe infarction [PDF]

open access: yes, 2014
Published in final edited form as: J Cogn Neurosci. 2014 June ; 26(6): 1266–1282. doi:10.1162/jocn_a_00538.We studied patient JS, who had a right occipital infarct that encroached on visual areas V1, V2v, and VP. When tested psychophysically, he was very
Buonanno, Ferdinando   +5 more
core   +1 more source

RPGR-associated retinal degeneration in human X-linked RP and a murine model [PDF]

open access: yes, 2012
PURPOSE. We investigated the retinal disease due to mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in human patients and in an Rpgr conditional knockout (cko) mouse model. METHODS. XLRP patients with RPGR-ORF15 mutations (n = 35, ages
Bell, Peter   +13 more
core   +1 more source

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