Results 41 to 50 of about 2,719 (152)
Study workflow. Neuroretinal changes were observed in alloxan‐induced diabetic rabbits, while the retinal vasculature remained unaffected, indicating the successful establishment of a diabetic neuroretinal model. Abstract Background Diabetic retinal neuropathy (DRN) leads to significant visual impairment; however, no existing animal model fully ...
Xinlu Li +9 more
wiley +1 more source
Multifocal Electroretinography in Assessment Of Diseases Of Posterior Pole Of Retina
Multifocal electroretinography (mfERG) based on the m-sequence stimulation technique which allows quick simultaneous recording of many local electroretinograms from the posterior pole.
Geeta B. Nair +4 more
core +1 more source
Abstract Background Indoleamine 2,3‐dioxygenase 1 (IDO1) is a heme‐containing enzyme that degrades tryptophan (Trp) to kynurenine (Kyn), which suppresses effector T cells and reduces antitumor activity. KHK2455 is a long‐acting selective IDO1 inhibitor that blocks the heme component of the IDO holoenzyme.
Timothy A. Yap +16 more
wiley +1 more source
To calculate the sensitivity and specificity of multifocal electroretinography (mfERG) in detection of chloroquine and hydroxychloroquine retinal toxicity, 120 eyes of 63 patients were evaluated using the currently recommended diagnostic tests.
Ahmadi Pirshahid, Sina
core +2 more sources
Consensus guidelines for nomenclature of companion animal inherited retinal disorders
Abstract Companion animals, namely dogs, cats, and horses, can be affected with many forms of hereditary retinal disease. The number of such diseases characterized in the last decade has increased substantially, and nomenclature is nonstandardized, heterogenous, and confusing.
Freya M. Mowat +3 more
wiley +1 more source
Purpose: To investigate the clinical potential of multifocal electroretinography (mf-ERG) for the evaluation of residual retinal function in retinitis pigmentosa (RP). Methods: From a group of 41 patients with RP examined for full-field and mf-ERGs, 24 patients were selected in whom the full-field ERGs were non-detectable. Data from the mf-ERGs of this
Sun Young Jang +2 more
openaire +1 more source
Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants
Mutations in ARSG are a very rare cause of Usher disease, assigned as “Usher type IV.” We identified 13 new subjects with mutations in ARSG, provide a clinical description of the subjects, and characterized the newly identified variants. Abstract Usher syndrome (USH) is the most common cause of deafblindness.
Miriam Bauwens +24 more
wiley +1 more source
Abstract Purpose This study measured associations between ON and OFF functional indicators and structural optical coherence tomography (OCT) and OCT angiography (OCTA) markers in diabetic retinal disease. Methods Fifty‐four participants with type 1 or type 2 diabetes (mean age = 34.1 years; range 18–60) and 48 age‐matched controls (mean age = 35.4 ...
Vanessa T. S. Tang +4 more
wiley +1 more source
Presumed X‐Linked Retinoschisis in a 3‐Month‐Old Baby Girl: A Case Report
Purpose The purpose of the study is to report a 3‐month‐old Iranian baby girl presenting with bilateral macular and peripheral retinoschisis with a probable diagnosis of X‐linked retinoschisis (XLRS). Methods The baby underwent an ophthalmic examination under general anesthesia revealing bilateral vitreous hemorrhage, spoke‐wheel pattern radiating from
Hanieh Fakhredin +5 more
wiley +1 more source
Objective The aim of this study is to report a case of bilateral foveal cysts in MPS I‐H resolving with oral acetazolamide and to highlight the diagnostic value of multimodal retinal imaging and electrophysiological testing. Introduction Hurler syndrome (mucopolysaccharidosis Type I‐H) is a lysosomal storage disorder that can cause progressive ...
Rashmi Lobo +3 more
wiley +1 more source

