Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Michalis, Georgiou"'
Autor:
Michalis Georgiou, Shaima Awadh Hashem, Michel Michaelides, Joseph G. Chacko, Sami H. Uwaydat
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102068- (2024)
Purpose: To present a case of molecularly confirmed oculocutaneous albinism (OCA) and retinitis pigmentosa (RP). Observations: A 46-year-old male with a lifelong established diagnosis of OCA and baseline best corrected visual acuity (BCVA) of 20/200,
Externí odkaz:
https://doaj.org/article/9c51b7b2f6d6418da6f4d61602eb7779
Publikováno v:
International Journal of Retina and Vitreous, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background The optimal timing of pars plana vitrectomy (PPV) following ocular trauma is an ongoing debate. Early vitrectomy post-trauma enables the rapid assessment of retinal disease by removing the scaffold that fosters proliferative vitre
Externí odkaz:
https://doaj.org/article/480760da0add4085bdf0a5a2813f98d5
Publikováno v:
BMJ Open Ophthalmology, Vol 8, Iss 1 (2023)
Background A five generation family has been analysed by whole exome sequencing (WES) for genetic associations with the multimorbidities of congenital cataract (CC), retinitis pigmentosa (RP) and Crohn’s disease (CD).Methods WES was performed for u
Externí odkaz:
https://doaj.org/article/5c412eb6c2ba48cabf610a7a324f86ac
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 28, Iss , Pp 101699- (2022)
Purpose: To present a case of unilateral IMPG2-associated adult onset vitelliform macular dystrophy (AVMD). Observations: A 68 year-old female presented with best corrected visual acuity (BCVA) of 20/20 and 20/40 for the right and left eye respective
Externí odkaz:
https://doaj.org/article/1ca431ddecb046c0b821966c01af74e8
Autor:
Michalis Georgiou, Naser Ali, Elizabeth Yang, Parampal S. Grewal, Tryfon Rotsos, Nikolas Pontikos, Anthony G. Robson, Michel Michaelides
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Purpose To present the detailed retinal phenotype of patients with Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy (LCA/EOSRD) caused by sequence variants in four genes, either not (n = 1) or very rarely (n = 3) previously as
Externí odkaz:
https://doaj.org/article/c1a623000c26418c94cae5c7edfa2317
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 23, Iss , Pp 101160- (2021)
Purpose: To present a case of atypical unilateral developmental retinal vascular anomaly. Observations: A 10-year-old girl presented to her paediatrician after an absent red reflex was noted in a photograph. She had right anisometropic amblyopia and
Externí odkaz:
https://doaj.org/article/a58691532b4141fe850e9ec96692be32
Autor:
Emily J. Patterson, PhD, Christopher S. Langlo, MD, PhD, Michalis Georgiou, MD, PhD, Angelos Kalitzeos, PhD, Mark E. Pennesi, MD, PhD, Jay Neitz, PhD, Alison J. Hardcastle, PhD, Maureen Neitz, PhD, Michel Michaelides, MD, PhD, Joseph Carroll, PhD
Publikováno v:
Ophthalmology Science, Vol 1, Iss 3, Pp 100047- (2021)
Purpose: To compare foveal hypoplasia and the appearance of the ellipsoid zone (EZ) at the fovea in patients with genetically confirmed achromatopsia (ACHM) and blue cone monochromacy (BCM). Design: Retrospective, multicenter observational study. Par
Externí odkaz:
https://doaj.org/article/8d70d9771b684c19af9149cae1227556
Autor:
Michalis Georgiou, Anthony G. Robson, Katarina Jovanovic, Thales A. C. de Guimarães, Naser Ali, Nikolas Pontikos, Sami H. Uwaydat, Omar A. Mahroo, Michael E. Cheetham, Andrew R. Webster, Alison J. Hardcastle, Michel Michaelides
Publikováno v:
Ophthalmology. 130:413-422
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63886c2774cb85c4940f30813e294ff9
https://doi.org/10.1016/j.ophtha.2022.11.015
https://doi.org/10.1016/j.ophtha.2022.11.015
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 19, Iss , Pp 100821- (2020)
Purpose: To describe the case of an asymptomatic 6-year-old girl, who was found to have bilateral dome-shaped macula, associated with left serous macular detachment and left optic disc pit, and no evidence of posterior staphyloma in either eye, and t
Externí odkaz:
https://doaj.org/article/b5d09845c6de422fb671284c390a8de2
Autor:
Amy Leung, Almudena Sacristan-Reviriego, Pedro R.L. Perdigão, Hali Sai, Michalis Georgiou, Angelos Kalitzeos, Amanda-Jayne F. Carr, Peter J. Coffey, Michel Michaelides, James Bainbridge, Michael E. Cheetham, Jacqueline van der Spuy
Publikováno v:
Stem Cell Reports. 17:2187-2202
Leber congenital amaurosis type 4 (LCA4), caused by AIPL1 mutations, is characterized by severe sight impairment in infancy and rapidly progressing degeneration of photoreceptor cells. We generated retinal organoids using induced pluripotent stem cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd48dd7e79bd2b59428b7b1ce5139f43
https://doi.org/10.1016/j.stemcr.2022.08.005
https://doi.org/10.1016/j.stemcr.2022.08.005