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The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypes.
Vacchiano V, Caporali L, La Morgia C, Carbonelli M, Amore G, Bartolomei I, Cascavilla ML, Barboni P, Lamperti C, Catania A, Chan JW, Karanja R, Sadun AA, Liguori R, Bianchi A, Gavazzi G, Mascalchi M, Salvi F, Carelli V. Vacchiano V, et al. Among authors: sadun aa. Mitochondrion. 2021 Sep;60:142-149. doi: 10.1016/j.mito.2021.08.007. Epub 2021 Aug 11. Mitochondrion. 2021. PMID: 34390870
Optic neuropathy in Lhon and Leigh syndrome.
Carelli V, Sadun AA. Carelli V, et al. Among authors: sadun aa. Ophthalmology. 2001 Jul;108(7):1172-3. doi: 10.1016/s0161-6420(01)00618-2. Ophthalmology. 2001. PMID: 11425664 No abstract available.
Mitochondrial dysfunction as a cause of optic neuropathies.
Carelli V, Ross-Cisneros FN, Sadun AA. Carelli V, et al. Among authors: sadun aa. Prog Retin Eye Res. 2004 Jan;23(1):53-89. doi: 10.1016/j.preteyeres.2003.10.003. Prog Retin Eye Res. 2004. PMID: 14766317 Review.
368 results