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Page 1
YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations.
Diaz J, Gérard X, Emerit MB, Areias J, Geny D, Dégardin J, Simonutti M, Guerquin MJ, Collin T, Viollet C, Billard JM, Métin C, Hubert L, Larti F, Kahrizi K, Jobling R, Agolini E, Shaheen R, Zigler A, Rouiller-Fabre V, Rozet JM, Picaud S, Novelli A, Alameer S, Najmabadi H, Cohn R, Munnich A, Barth M, Lugli L, Alkuraya FS, Blaser S, Gashlan M, Besmond C, Darmon M, Masson J. Diaz J, et al. Among authors: gashlan m. Brain. 2020 Oct 1;143(10):2911-2928. doi: 10.1093/brain/awaa235. Brain. 2020. PMID: 33103737
Safety and effectiveness of ataluren in patients with Duchenne muscular dystrophy: single-center experience from Saudi Arabia.
Ahmad M, ElRasoul A, Sedayou R, Tamboosi M, Mahroos H, Alrashed S, Tunkar M, Alzahrani F, Alharbi M, Aljehani M, Alahmari M, Alqarni K, Gashlan M, Yilmaz BS, Alshaikh NM. Ahmad M, et al. Among authors: gashlan m. J Int Med Res. 2024 Dec;52(12):3000605241305252. doi: 10.1177/03000605241305252. J Int Med Res. 2024. PMID: 39719075 Free PMC article.
Reading-induced absence seizures.
Singh B, Anderson L, al Gashlan M, al-Shahwan SA, Riela AR. Singh B, et al. Among authors: al gashlan m. Neurology. 1995 Aug;45(8):1623-4. doi: 10.1212/wnl.45.8.1623. Neurology. 1995. PMID: 7644067