Strategies for fighting mitochondrial diseases von Viscomi, C., Zeviani, M.

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AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome von Di Meo, I, Marchet, S, Lamperti, C, Zeviani, M, Viscomi, C

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Mitochondrial disorders von Zeviani, Massimo, Di Donato, Stefano

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Loss of apoptosis-inducing factor critically affects MIA40 function von Meyer, K, Buettner, S, Ghezzi, D, Zeviani, M, Bano, D, Nicotera, P

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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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Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk von Spinazzola, A., Zeviani, M.

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Reduced mitochondrial Ca2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase von Granatiero, V, Giorgio, V, Calì, T, Patron, M, Brini, M, Bernardi, P, Tiranti, V, Zeviani, M, Pallafacchina, G, De Stefani, D, Rizzuto, R

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Clinical and molecular features of mitochondrial DNA depletion syndromes von Spinazzola, A, Invernizzi, F, Carrara, F, Lamantea, E, Donati, A, DiRocco, M, Giordano, I, Meznaric-Petrusa, M, Baruffini, E, Ferrero, I, Zeviani, M

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Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells von Invernizzi, F, D'Amato, I, Jensen, P B, Ravaglia, S, Zeviani, M, Tiranti, V

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SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype von Quadalti, C., Brunetti, D., Lagutina, I., Duchi, R., Perota, A., Lazzari, G., Cerutti, R., Di Meo, I., Johnson, M., Bottani, E., Crociara, P., Corona, C., Grifoni, S., Tiranti, V., Fernandez-Vizarra, E., Robinson, A.J., Viscomi, C., Casalone, C., Zeviani, M., Galli, C.

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Revisiting mitochondrial ocular myopathies: a study from the Italian Network von Orsucci, D., Angelini, C., Bertini, E., Carelli, V., Comi, G. P., Federico, A., Minetti, C., Moggio, M., Mongini, T., Santorelli, F. M., Servidei, S., Tonin, P., Ardissone, A., Bello, L., Bruno, C., Ienco, E. Caldarazzo, Diodato, D., Filosto, M., Lamperti, C., Moroni, I., Musumeci, O., Pegoraro, E., Primiano, G., Ronchi, D., Rubegni, A., Salvatore, S., Sciacco, M., Valentino, M. L., Vercelli, L., Toscano, A., Zeviani, M., Siciliano, G., Mancuso, M.

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Clinical and molecular findings in children with complex I deficiency von Bugiani, M., Invernizzi, F., Alberio, S., Briem, E., Lamantea, E., Carrara, F., Moroni, I., Farina, L., Spada, M., Donati, M.A., Uziel, G., Zeviani, M.

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Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance von KAUKONEN, J, JUSELLUS, J. K, TIRANTI, V, KYTTÄLÄ, A, ZEVIANI, M, COMI, G. P, KERÄNEN, S, PELTONEN, L, SUOMALAINEN, A

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Properties of a sandy clay loam Haplic Ferralsol and soybean grain yield in a five-year field trial as affected by biochar amendment von Madari, Beata E., Silva, Mellissa A.S., Carvalho, Márcia T.M., Maia, Aline H.N., Petter, Fabiano A., Santos, Janne L.S., Tsai, Siu M., Leal, Wesley G.O., Zeviani, Walmes M.

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Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase γ mutations von WINTERTHUN, S, FERRARI, G, HE, L, TAYLOR, R. W, ZEVIANI, M, TURNBULL, D. M, ENGELSEN, B. A, MOEN, G, BINDOFF, L. A

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Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease von Uusimaa, J, Jungbluth, H, Fratter, C, Crisponi, G, Feng, L, Zeviani, M, Hughes, I, Treacy, E P, Birks, J, Brown, G K, Sewry, C A, McDermott, M, Muntoni, F, Poulton, J

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Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases von Mancuso, M, Angelini, C, Bertini, E, Carelli, V, Comi, G.P, Minetti, C, Moggio, M, Mongini, T, Servidei, S, Tonin, P, Toscano, A, Uziel, G, Zeviani, M, Siciliano, G

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Local and systemic control of powdery mildew in eucalyptus using essential oils and decoctions from traditional Brazilian medicinal plants von Silva, A. C, Souza, P. E, Resende, M. L. V, Silva, M. B. Jr, Ribeiro, P. M. Jr, Zeviani, W. M, Zhou, D

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GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy von BUGIANI, M, AL SHAHWAN, S, LAMANTEA, E, BIZZI, A, BAKHSH, E, MORONI, I, BALESTRINI, M. R, UZIEL, G, ZEVIANI, M

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M.I.3 Nuclear genes involved in mitochondrial syndromes von Zeviani, M

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