Rezultaty - Margherita Verardo
- Rezultaty 1 - 5 Rezultaty od 5
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Oxidative stress in Duchenne muscular dystrophy: focus on the NRF2 redox pathway od Sara Petrillo, Laura Pelosi, Fiorella Piemonte, Lorena Travaglini, Laura Forcina, Michela Catteruccia, Stefania Petrini, Margherita Verardo, Adele D’Amico, Antonio Musarò, Enrico Bertini
Wydane 2017Artigo -
3
A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease od Daria Diodato, Giorgio Tasca, Daniela Verrigni, Adele D’Amico, Teresa Rizza, Giulia Tozzi, Diego Martinelli, Margherita Verardo, Federica Invernizzi, Alessia Nasca, Emanuele Bellacchio, Daniele Ghezzi, Fiorella Piemonte, Carlo Dionisi‐Vici, Rosalba Carrozzo, Enrico Bertini
Wydane 2015Artigo -
4
Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort od Michela Catteruccia, Fabiana Fattori, Valentina Codemo, Lucia Ruggiero, Lorenzo Maggi, Giorgio Tasca, Chiara Fiorillo, Marika Pane, Angela Berardinelli, Margherita Verardo, Cinzia Bragato, Marina Mora, Lucia Morandi, Claudio Bruno, Lucio Santoro, Elena Pegoraro, Eugenio Mercuri, Enrico Bertini, Adele D’Amico
Wydane 2013Artigo -
5
Clinical-genetic features and peculiar muscle histopathology in infantile<i>DNM1L</i>-related mitochondrial epileptic encephalopathy od Daniela Verrigni, Michela Di Nottia, Anna Ardissone, Enrico Baruffini, Alessia Nasca, Andrea Legati, Emanuele Bellacchio, Gigliola Fagiolari, Diego Martinelli, Lucia Fusco, Domenica Battaglia, Giulia Trani, Gianmarco Versienti, Silvia Marchet, Alessandra Torraco, Teresa Rizza, Margherita Verardo, Adele D’Amico, Daria Diodato, Isabella Moroni, Costanza Lamperti, Stefania Petrini, Maurizio Moggio, P Goffrini, Daniele Ghezzi, Rosalba Carrozzo, Enrico Bertini
Wydane 2019Artigo
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