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Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.
Achilli A, Iommarini L, Olivieri A, Pala M, Hooshiar Kashani B, Reynier P, La Morgia C, Valentino ML, Liguori R, Pizza F, Barboni P, Sadun F, De Negri AM, Zeviani M, Dollfus H, Moulignier A, Ducos G, Orssaud C, Bonneau D, Procaccio V, Leo-Kottler B, Fauser S, Wissinger B, Amati-Bonneau P, Torroni A, Carelli V. Achilli A, et al. Among authors: sadun f. PLoS One. 2012;7(8):e42242. doi: 10.1371/journal.pone.0042242. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22879922 Free PMC article.
MOG-IgG positive optic neuritis after SARS-CoV-2 infection.
Gilardi M, Cortese A, Ferraro E, Rispoli M, Sadun R, Altavista MC, Sadun F. Gilardi M, et al. Among authors: sadun f. Eur J Ophthalmol. 2023 Sep;33(5):NP87-NP90. doi: 10.1177/11206721221136319. Epub 2022 Nov 1. Eur J Ophthalmol. 2023. PMID: 36317310 Free PMC article.
Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
Quiros PA, Torres RJ, Salomao S, Berezovsky A, Carelli V, Sherman J, Sadun F, De Negri A, Belfort R, Sadun AA. Quiros PA, et al. Among authors: sadun aa, sadun f. Br J Ophthalmol. 2006 Feb;90(2):150-3. doi: 10.1136/bjo.2005.074526. Br J Ophthalmol. 2006. PMID: 16424523 Free PMC article.
42 results