Keeping in shape the dogma of mitochondrial DNA maternal inheritance. by Valerio Carelli

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Metformin may alter the course of Leber’s hereditary optic neuropathy: a case report by Shenoda Abd Elmaseh, Danielle A. Gauthier, Danielle A. Gauthier, Maryam Golmohammadi, Maryam Golmohammadi, Nutsa Pargalava, Valerio Carelli, Valerio Carelli, Alfredo A. Sadun, Alfredo A. Sadun

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Late-onset Leber’s hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link? by Giulia Amore, Giulia Amore, Michele Carbonelli, Diego D’Angeli, Luigi Bonan, Marco Faustini-Fustini, Alessandra Maresca, Valerio Carelli, Valerio Carelli, Chiara La Morgia, Chiara La Morgia

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Case Report: Novel ATP13A2 pathogenic variants associated with early-onset parkinsonism and a mini-review by Leonardo Affronte, Leonardo Affronte, Antonella Pini, Claudia Pizzoli, Emanuele Coccia, Serena Mazzone, Arber Golemi, Melania Giannotta, Duccio Maria Cordelli, Duccio Maria Cordelli, Valerio Carelli, Valerio Carelli, Alessandro Vaisfeld, Alessandro Vaisfeld, Flavia Palombo

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The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. by Anna Ghelli, Anna Maria Porcelli, Claudia Zanna, Sara Vidoni, Stefano Mattioli, Anna Barbieri, Luisa Iommarini, Maria Pala, Alessandro Achilli, Antonio Torroni, Michela Rugolo, Valerio Carelli

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Secondary post-geniculate involvement in Leber's hereditary optic neuropathy. by Giovanni Rizzo, Kevin R Tozer, Caterina Tonon, David Manners, Claudia Testa, Emil Malucelli, Maria Lucia Valentino, Chiara La Morgia, Piero Barboni, Ruvdeep S Randhawa, Fred N Ross-Cisneros, Alfredo A Sadun, Valerio Carelli, Raffaele Lodi

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A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy by Nneka Southwell, Guido Primiano, Viraj Nadkarni, Nabeel Attarwala, Emelie Beattie, Dawson Miller, Sumaitaah Alam, Irene Liparulo, Yevgeniya I Shurubor, Maria Lucia Valentino, Valerio Carelli, Serenella Servidei, Steven S Gross, Giovanni Manfredi, Qiuying Chen, Marilena D'Aurelio

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Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements. by Michele Carbonelli, Chiara La Morgia, Giacomo Savini, Maria Lucia Cascavilla, Enrico Borrelli, Filipe Chicani, Carolina do V F Ramos, Solange R Salomao, Vincenzo Parisi, Jerry Sebag, Francesco Bandello, Alfredo A Sadun, Valerio Carelli, Piero Barboni

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Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early‐onset arteriopathy and cavitating leukoencephalopathy by Tommaso Pippucci, Alessandra Maresca, Pamela Magini, Giovanna Cenacchi, Vincenzo Donadio, Flavia Palombo, Valentina Papa, Alex Incensi, Giuseppe Gasparre, Maria Lucia Valentino, Carmela Preziuso, Annalinda Pisano, Michele Ragno, Rocco Liguori, Carla Giordano, Caterina Tonon, Raffaele Lodi, Antonia Parmeggiani, Valerio Carelli, Marco Seri

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The origin of modern North Africans as depicted by a massive survey of mitogenomes by Giulia Colombo, Elisabetta Moroni, Alessandro Raveane, Nicola Rambaldi Migliore, Vincenzo Agostini, Rosalinda Di Gerlando, Claudio Fiorini, Leonardo Caporali, Francesca Gandini, Elena Raimondi, Eugenia D’Atanasio, Hovirag Lancioni, Valerio Carelli, Maria Pala, Beniamino Trombetta, Andrea Novelletto, Jean-Michel Dugoujon, Alessandro Achilli, Antonio Torroni, Martin B. Richards, Fulvio Cruciani, Ornella Semino, Anna Olivieri

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

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Genotype-specific effects of elamipretide in patients with primary mitochondrial myopathy: a post hoc analysis of the MMPOWER-3 trial by Amel Karaa, Enrico Bertini, Valerio Carelli, Bruce Cohen, Gregory M. Ennes, Marni J. Falk, Amy Goldstein, Gráinne Gorman, Richard Haas, Michio Hirano, Thomas Klopstock, Mary Kay Koenig, Cornelia Kornblum, Costanza Lamperti, Anna Lehman, Nicola Longo, Maria Judit Molnar, Sumit Parikh, Han Phan, Robert D. S. Pitceathly, Russekk Saneto, Fernando Scaglia, Serenella Servidei, Mark Tarnopolsky, Antonio Toscano, Johan L. K. Van Hove, John Vissing, Jerry Vockley, Jeffrey S. Finman, Anthony Abbruscato, David A. Brown, Alana Sullivan, James A. Shiffer, Michelango Mancuso, on behalf of the MMPOWER-3 Trial Investigators

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