Primary mitochondrial optic neuropathies von Barboni, P.

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Leber's hereditary optic neuropathy: the ophthalmologist point of view von Barboni, P.

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Vascular supply in mitochondrial optic neuropathy and glaucoma von Barboni, P.

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Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies von Manners, D N, Rizzo, G, La Morgia, C, Tonon, C, Testa, C, Barboni, P, Malucelli, E, Valentino, M L, Caporali, L, Strobbe, D, Carelli, V, Lodi, R

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Idebenone Treatment In Leber's Hereditary Optic Neuropathy von Carelli, Valerio, La Morgia, Chiara, Valentino, Maria Lucia, Rizzo, Giovanni, Carbonelli, Michele, De Negri, Anna Maria, Sadun, Federico, Carta, Arturo, Guerriero, Silvana, Simonelli, Francesca, Sadun, Alfredo Arrigo, Aggarwal, Divya, Liguori, Rocco, Avoni, Patrizia, Baruzzi, Agostino, Zeviani, Massimo, Montagna, Pasquale, Barboni, Piero

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Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? von La Morgia, C., Barboni, P., Rizzo, G., Carbonelli, M., Savini, G., Scaglione, C., Capellari, S., Bonazza, S., Giannoccaro, M. P., Calandra-Buonaura, G., Liguori, R., Cortelli, P., Martinelli, P., Baruzzi, A., Carelli, V.

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OCT angiography in mitochondrial optic neuropathies von Barboni, P., Balducci, N.

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Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study von Savini, G, Zanini, M, Carelli, V, Sadun, A A, Ross-Cisneros, F N, Barboni, P

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Neurological involvement in mitochondrial eye diseases von La Morgia, C., Caporali, L., Di Vito, L., Carbonelli, M., Valentino, M.L., Liguori, R., Barboni, P., Carelli, V.

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Effect of pupil dilation on retinal nerve fibre layer thickness measurements and their repeatability with Cirrus HD-OCT von Savini, G, Carbonelli, M, Parisi, V, Barboni, P

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Optical coherence tomography in the differential diagnosis of true edema versus pseudoedema of the optic disc von Gozzi, F., Aldigeri, R., Mora, P., Bianchi‐Marzoli, S., Barboni, P., Gandolfi, S., Farci, R., Fossarello, M., Incerti, M., Carta, A.

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Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus von LA MORGIA, C, ACHILLI, A, VETRUGNO, R, MOSTACCI, B, LIGUORI, R, CARROCCIA, R, MONTAGNA, P, RUGOLO, M, TORRONI, A, CARELLI, V, IOMMARINI, L, BARBONI, P, PALA, M, OLIVIERI, A, ZANNA, C, VIDONI, S, TONON, C, LODI, R

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International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy von Carelli, Valerio, Carbonelli, Michele, de Coo, Irenaeus F, Kawasaki, Aki, Klopstock, Thomas, Lagrèze, Wolf A, La Morgia, Chiara, Newman, Nancy J, Orssaud, Christophe, Pott, Jan Willem R, Sadun, Alfredo A, van Everdingen, Judith, Vignal-Clermont, Catherine, Votruba, Marcela, Yu-Wai-Man, Patrick, Barboni, Piero

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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder von Del Dotto, Valentina, Ullah, Farid, Di Meo, Ivano, Magini, Pamela, Gusic, Mirjana, Maresca, Alessandra, Caporali, Leonardo, Palombo, Flavia, Tagliavini, Francesca, Baugh, Evan Harris, Macao, Bertil, Szilagyi, Zsolt, Peron, Camille, Gustafson, Margaret A., Khan, Kamal, La Morgia, Chiara, Barboni, Piero, Carbonelli, Michele, Valentino, Maria Lucia, Liguori, Rocco, Shashi, Vandana, Sullivan, Jennifer, Nagaraj, Shashi, El-Dairi, Mays, Iannaccone, Alessandro, Cutcutache, Ioana, Bertini, Enrico, Carrozzo, Rosalba, Emma, Francesco, Diomedi-Camassei, Francesca, Zanna, Claudia, Armstrong, Martin, Page, Matthew, Stong, Nicholas, Boesch, Sylvia, Kopajtich, Robert, Wortmann, Saskia, Sperl, Wolfgang, Davis, Erica E., Copeland, William C., Seri, Marco, Falkenberg, Maria, Prokisch, Holger, Katsanis, Nicholas, Tiranti, Valeria, Pippucci, Tommaso, Carelli, Valerio

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The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype von Valentino, M L, Barboni, P, Rengo, C, Achilli, A, Torroni, A, Lodi, R, Tonon, C, Barbiroli, B, Fortuna, F, Montagna, P, Baruzzi, A, Carelli, V

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Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy von Achilli, Alessandro, Iommarini, Luisa, Olivieri, Anna, Pala, Maria, Hooshiar Kashani, Baharak, Reynier, Pascal, La Morgia, Chiara, Valentino, Maria Lucia, Liguori, Rocco, Pizza, Fabio, Barboni, Piero, Sadun, Federico, De Negri, Anna Maria, Zeviani, Massimo, Dollfus, Helene, Moulignier, Antoine, Ducos, Ghislaine, Orssaud, Christophe, Bonneau, Dominique, Procaccio, Vincent, Leo-Kottler, Beate, Fauser, Sascha, Wissinger, Bernd, Amati-Bonneau, Patrizia, Torroni, Antonio, Carelli, Valerio

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Idebenone treatment in patients with OPA1-mutant dominant optic atrophy von Barboni, Piero, Valentino, Maria Lucia, La Morgia, Chiara, Carbonelli, Michele, Savini, Giacomo, De Negri, Annamaria, Simonelli, Francesca, Sadun, Federico, Caporali, Leonardo, Maresca, Alessandra, Liguori, Rocco, Baruzzi, Agostino, Zeviani, Massimo, Carelli, Valerio

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Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy von Lodi, R, Carelli, V, Cortelli, P, Iotti, S, Valentino, M L, Barboni, P, Pallotti, F, Montagna, P, Barbiroli, B

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Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy von Barboni, Piero, Savini, Giacomo, Valentino, Maria Lucia, Montagna, Pasquale, Cortelli, Pietro, De Negri, Anna Maria, Sadun, Federico, Bianchi, Stefania, Longanesi, Lora, Zanini, Maurizio, de Vivo, Antonello, Carelli, Valerio

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Medical management of hereditary optic neuropathies von La Morgia, Chiara, Carbonelli, Michele, Barboni, Piero, Sadun, Alfredo Arrigo, Carelli, Valerio

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