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Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB).
Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, Matri KE, Matri LE, Schorderet DF. Habibi I, et al. Among authors: schorderet df. Genes (Basel). 2019 Nov 21;10(12):953. doi: 10.3390/genes10120953. Genes (Basel). 2019. PMID: 31766397 Free PMC article.
Genetic spectrum of retinal dystrophies in Tunisia.
Habibi I, Falfoul Y, Turki A, Hassairi A, El Matri K, Chebil A, Schorderet DF, El Matri L. Habibi I, et al. Among authors: schorderet df. Sci Rep. 2020 Jul 8;10(1):11199. doi: 10.1038/s41598-020-67792-y. Sci Rep. 2020. PMID: 32641690 Free PMC article.
Identifying mutations in Tunisian families with retinal dystrophy.
Habibi I, Chebil A, Falfoul Y, Allaman-Pillet N, Kort F, Schorderet DF, El Matri L. Habibi I, et al. Among authors: schorderet df. Sci Rep. 2016 Nov 22;6:37455. doi: 10.1038/srep37455. Sci Rep. 2016. PMID: 27874104 Free PMC article.
Analysis of Inherited Optic Neuropathies.
Lazdinyte S, Schorderet DF, Schaller A, Valmaggia C, Todorova MG. Lazdinyte S, et al. Among authors: schorderet df. Klin Monbl Augenheilkd. 2019 Apr;236(4):451-461. doi: 10.1055/a-0829-6828. Epub 2019 Mar 4. Klin Monbl Augenheilkd. 2019. PMID: 30831606 English.
Prominent Optic Disc Featured in Inherited Retinopathy.
Todorova MG, Bojinova RI, Valmaggia C, Schorderet DF. Todorova MG, et al. Among authors: schorderet df. Klin Monbl Augenheilkd. 2017 Apr;234(4):577-583. doi: 10.1055/s-0042-121335. Epub 2017 Feb 1. Klin Monbl Augenheilkd. 2017. PMID: 28147405 English.
285 results