Retinal phenotyping of variants of Alzheimer's disease using ultra‐widefield retinal images

Autor: Lajos Csincsik, Nicola Quinn, Keir X. X. Yong, Sebastian J. Crutch, Tunde Peto, Imre Lengyel

Publikováno v: Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 13, Iss 1, Pp n/a-n/a (2021)

Abstract Background Posterior cortical atrophy (PCA) is the most common atypical variant of Alzheimer's disease (AD). Changes associated with PCA in the brain affect the visual cortex, but little is known about retinal changes in PCA. In this study,

Externí odkaz: https://doaj.org/article/9891c1c33a994349a1cf1170ef21936d

Retinal phenotyping of variants of Alzheimer’s disease using colour ultra-widefield laser scanning ophthalmoscopic images

Autor: Csincsik, Lajos, Quinn, Nicola, Yong, Keir X X, Crutch, Sebastian J, Peto, Tunde, Lengyel, Imre

Publikováno v: Csincsik, L, Quinn, N, Yong, K X X, Crutch, S J, Peto, T & Lengyel, I 2021, ' Retinal phenotyping of variants of Alzheimer’s disease using colour ultra-widefield laser scanning ophthalmoscopic images ', Alzheimer's & dementia : the journal of the Alzheimer's Association, vol. 13, no. 1, e12232 . https://doi.org/10.1002/dad2.12232

BACKGROUND:Posterior cortical atrophy (PCA) is the most common atypical variant of Alzheimer’s (AD) disease. Changes associated with PCA in the brain affect the visual cortex, but little is known whether there are retinal changes associated to with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2607::2a063955efcbd47be6e5f9f43ea50d00
https://pure.qub.ac.uk/en/publications/b7ba9830-6934-4444-9eac-b1e7f8fd5bbe

Acquired retinal pigmentary degeneration in a child with 13q deletion syndrome

Autor: Kara M. Cavuoto, Peter J. Belin, Zenia P. Aguilera, Craig A. McKeown, Parul Jayakar

Publikováno v: Journal of American Association for Pediatric Ophthalmology and Strabismus. 19:482-484

Orbeli syndrome, or 13q deletion syndrome, is a rare condition caused by a distal deletion in the long arm of chromosome 13. The syndrome is characterized by severe physical malformations and developmental delays and has been associated with numerous

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f296a1d3621d9979fc431a482d9249b
https://doi.org/10.1016/j.jaapos.2015.05.021

Le vitré du myope : quelles anomalies importantes peut-on déceler en périphérie ?

Autor: I. Hubert, J.-P. Berrod

Publikováno v: Journal Français d'Ophtalmologie. 35:378-386

Resume La peripherie vitreo-retinienne du myope peut presenter des anomalies dont la frequence et la severite sont correlees a la longueur axiale du globe. Il s’agit du blanc sans pression, du givre, des palissades, des migrations pigmentaires ou d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b8c1ff7750fbe38588e6a5b54de58e28
https://doi.org/10.1016/j.jfo.2012.02.006

Mental Retardation and Neurologic Involvement in Patients with Congenital Retinal Blindness

Autor: Anatole S. Dekaban

Publikováno v: Developmental Medicine & Child Neurology. 14:436-444

SUMMARY Congenital retinal blindness is a recessively inherited disorder which occurs in about 10 per cent of blind children. The salient features are blindness or near-blindness since birth or early months of life, absent or attenuated electroretino

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716a7212153f4658d356f790b6aae5b4
https://doi.org/10.1111/j.1469-8749.1972.tb02616.x