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Nanotopography by chromatic confocal microscopy of the endothelium in Fuchs endothelial corneal dystrophy, pseudophakic bullous keratopathy and healthy corneas.
Vaitinadapoulé H, Poinard S, He Z, Pascale-Hamri A, Thomas J, Gain P, Thuret JY, Mascarelli F, Thuret G; French Fuchs Study Group (FFSG). Vaitinadapoulé H, et al. Among authors: mascarelli f. Br J Ophthalmol. 2023 Sep 15:bjo-2023-323297. doi: 10.1136/bjo-2023-323297. Online ahead of print. Br J Ophthalmol. 2023. PMID: 37714683
[No title available]
[No authors listed] [No authors listed] PMID: 37604553
[No title available]
[No authors listed] [No authors listed] PMID: 37604543
[New lighting technology and our eyes].
Torriglia A, Mascarelli F, Behar-Cohen F. Torriglia A, et al. Among authors: mascarelli f. Med Sci (Paris). 2020 Aug-Sep;36(8-9):769-773. doi: 10.1051/medsci/2020133. Epub 2020 Aug 21. Med Sci (Paris). 2020. PMID: 32821054 Free article. Review. French.
Mechanisms of FH Protection Against Neovascular AMD.
Borras C, Delaunay K, Slaoui Y, Abache T, Jorieux S, Naud MC, Sanharawi ME, Gelize E, Lassiaz P, An N, Kowalczuk L, Ayassami C, Moulin A, Behar-Cohen F, Mascarelli F, Dinet V. Borras C, et al. Among authors: mascarelli f. Front Immunol. 2020 Apr 3;11:443. doi: 10.3389/fimmu.2020.00443. eCollection 2020. Front Immunol. 2020. PMID: 32318056 Free PMC article.
Sostdc1 is expressed in all major compartments of developing and adult mammalian eyes.
Valensi M, Goldman G, Marchant D, Van Den Berghe L, Jonet L, Daruich A, Robert MP, Krejci E, Klein C, Mascarelli F, Versaux-Botteri C, Moulin A, Putterman M, Guimiot F, Molina T, Terris B, Brémond-Gignac D, Behar-Cohen F, Abitbol MM. Valensi M, et al. Among authors: mascarelli f. Graefes Arch Clin Exp Ophthalmol. 2019 Nov;257(11):2401-2427. doi: 10.1007/s00417-019-04462-4. Epub 2019 Sep 16. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 31529323
Amyloidosis in Retinal Neurodegenerative Diseases.
Masuzzo A, Dinet V, Cavanagh C, Mascarelli F, Krantic S. Masuzzo A, et al. Among authors: mascarelli f. Front Neurol. 2016 Aug 8;7:127. doi: 10.3389/fneur.2016.00127. eCollection 2016. Front Neurol. 2016. PMID: 27551275 Free PMC article. Review.
Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Dinet V, Ciccotosto GD, Delaunay K, Borras C, Ranchon-Cole I, Kostic C, Savoldelli M, El Sanharawi M, Jonet L, Pirou C, An N, Abitbol M, Arsenijevic Y, Behar-Cohen F, Cappai R, Mascarelli F. Dinet V, et al. Among authors: mascarelli f. Mol Brain. 2016 Jun 8;9(1):64. doi: 10.1186/s13041-016-0245-z. Mol Brain. 2016. PMID: 27267879 Free PMC article.
61 results