Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Razek Georges Coussa"'
Autor:
Mahsaw Mansoor, Razek Georges Coussa, Margaret R. Strampe, Scott A. Larson, Jonathan F. Russell
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 29, Iss , Pp 101798- (2023)
Purpose: To describe a novel case of Norrie disease and X-linked Kabuki syndrome caused by a microdeletion encompassing multiple genes on the X chromosome. Observations: A 3-day-old boy born at full term had bilateral retrolental fibrovascular plaque
Externí odkaz:
https://doaj.org/article/fb780eeb5914483893888a5892956e48
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 10, Iss , Pp 18-24 (2018)
Purpose: To report the longest ophthalmic follow-up and the associated ocular complications of HLA-A29 negative Birdshot-like chorioretinopathy (BLCR) associated with common variable immunodeficiency (CVID). Observations: A 22-year-old man known for
Externí odkaz:
https://doaj.org/article/33cc42ef44f44f9cbdd977e0691b1af2
Autor:
Razek Georges Coussa, Susan M. Wakil, Hady Saheb, David E. Lederer, Karin M. Oliver, Devinder P. Cheema
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 5, Iss C, Pp 16-19 (2017)
Purpose: To report the occurrence and management of severe infectious scleritis in a 75 year-old woman following intravitreal ranibizumab injection. Observations: A 75 year-old monocular woman receiving monthly intravitreal ranibizumab injection for
Externí odkaz:
https://doaj.org/article/e6dfadae1e7049459ea6562065f9e794
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 5, Iss C, Pp 11-15 (2017)
Purpose: To describe a case of Crohn disease presenting as occlusive vasculitis resulting in a central retinal artery occlusion (CRAO) in one eye and transient ischemic optic neuropathy in the fellow eye. Observations: An 18-year-old patient recently
Externí odkaz:
https://doaj.org/article/69ae438a8354462e991056925c9cb9d9
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 8, Iss C, Pp 1-3 (2017)
Purpose: To report the first sequential cross-over treatment with the longest ophthalmic follow-up in a case of X-linked juvenile retinoschisis (XLRS) successfully treated with topical dorzolamide. Observations: A healthy 34 year-old man presented wi
Externí odkaz:
https://doaj.org/article/28b0095550af479ca4ec069bea085804
Autor:
Ian C. Han, Razek Georges Coussa, Mahsaw Mansoor, D. Brice Critser, Elliott H. Sohn, Jonathan F. Russell, Edwin M. Stone
Publikováno v:
Ophthalmology Retina. 7:441-449
Choroidal neovascularization (CNV) is usually considered to be a late-stage complication in Best vitelliform macular dystrophy (BVMD) and can be difficult to diagnose with fluorescein angiography. This study used swept-source optical coherence tomogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5164f846d878bd3b60fe5d3b89157917
https://doi.org/10.1016/j.oret.2022.11.014
https://doi.org/10.1016/j.oret.2022.11.014
Autor:
Jacob Lynn, Austin Raney, Nathaniel Britton, Josh Ramoin, Ryan W. Yang, Bojana Radojevic, Cynthia K. McClard, Ronald Kingsley, Razek Georges Coussa, Lea D. Bennett
Publikováno v:
Genes; Volume 14; Issue 1; Pages: 74
The overlapping genetic and clinical spectrum in inherited retinal degeneration (IRD) creates challenges for accurate diagnoses. The goal of this work was to determine the genetic diagnosis and clinical features for patients diagnosed with an IRD. Af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edc337eaca20911576230ba2733bd87
Autor:
Christine Yergeau, Razek Georges Coussa, Fares Antaki, Catherine Argyriou, Robert K. Koenekoop, Nancy E. Braverman
BackgroundZellweger Spectrum Disorder (ZSD) is caused by bi-allelic defects in any of 13PEXgenes, resulting in failure to form functional peroxisomes. Individuals manifest a wide spectrum of clinical phenotypes and severity, but almost all have retin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c32fb58a1c2db20ea29e74ceb3b3ef66
https://doi.org/10.1101/2022.11.06.22279732
https://doi.org/10.1101/2022.11.06.22279732
Publikováno v:
Ophthalmic Genetics. 42:420-430
Purpose: The mitochondrial DNA A3243G (m.3243A>G) variant causes a wide spectrum of phenotypes, with pigmentary retinopathy as the most common ocular finding. We undertook this meta-analysis to investigate the clinical course of visual acuity (VA) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919362fe64b8da36840f02b5fd94bbcb
https://doi.org/10.1080/13816810.2021.1907598
https://doi.org/10.1080/13816810.2021.1907598
Autor:
Julia Sebag, Mikael Sebag, Renaud Duval, Anthony Fanous, Razek Georges Coussa, Ghofril Kahwati, Fares Antaki
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports
Scientific Reports
We aimed to assess the feasibility of machine learning (ML) algorithm design to predict proliferative vitreoretinopathy (PVR) by ophthalmologists without coding experience using automated ML (AutoML). The study was a retrospective cohort study of 506
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8902a9184c532b0ef2e2546f830700f
http://link.springer.com/article/10.1038/s41598-020-76665-3
http://link.springer.com/article/10.1038/s41598-020-76665-3