Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Brancaccio, Arianna"'
Autor:
Brancaccio, Arianna
Stroke is the main cause of adult motor disability. Nevertheless, recent meta-analyses show that the theoretical models conceived to explain the post-stroke brain reorganization are inaccurate and therefore misleading in laying the theoretical founda
Externí odkaz:
https://hdl.handle.net/11572/371068
Autor:
Mahmoud, Wala, Baur, David, Zrenner, Brigitte, Brancaccio, Arianna, Belardinelli, Paolo, Ramos-Murguialday, Ander, Zrenner, Christoph, Ziemann, Ulf
Publikováno v:
Frontiers in Neurology; 2024, p01-15, 15p
Autor:
Tabarelli, Davide1 (AUTHOR) davide.tabarelli@unitn.it, Brancaccio, Arianna1 (AUTHOR) arianna.brancaccio@unitn.it, Zrenner, Christoph2 (AUTHOR) christoph.zrenner@gmail.com, Belardinelli, Paolo1,3 (AUTHOR) paolo.belardinelli@unitn.it
Publikováno v:
Brain Sciences (2076-3425). Mar2022, Vol. 12 Issue 3, p348. 17p.
Autor:
Brancaccio, Arianna1 arianna.brancaccio@unitn.it, Tabarelli, Davide1, Bigica, Marco1, Baldauf, Daniel1
Publikováno v:
Scientific Reports. 4/24/2020, Vol. 10 Issue 1, p1-15. 15p.
Autor:
Nikolic, Ana, Jones, Takako, Govi, Monica, Mele, Fabiano, Maranda, Louise, Sera, Francesco, Ricci, Giulia, Ruggiero, Lucia, Vercelli, Liliana, Portaro, Simona, Villa, Luisa, Fiorillo, Chiara, Maggi, Lorenzo, Santoro, Lucio, Antonini, Giovanni, Filosto, Massimiliano, Moggio, Maurizio, Angelini, Corrado, Pegoraro, Elena, Berardinelli, Angela, Maioli, Maria Antonetta, D’Angelo, Grazia, Di Muzio, Antonino, Siciliano, Gabriele, Tomelleri, Giuliano, D’Esposito, Maurizio, Della Ragione, Floriana, Brancaccio, Arianna, Piras, Rachele, Rodolico, Carmelo, Mongini, Tiziana, Magdinier, Frédérique, Salsi, Valentina, Jones, Peter, Tupler, Rossella
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, 2020, 21 (7), pp.2635. ⟨10.3390/ijms21072635⟩
International Journal of Molecular Sciences, Vol 21, Iss 2635, p 2635 (2020)
International Journal of Molecular Sciences, MDPI, 2020, 21 (7), pp.2635. ⟨10.3390/ijms21072635⟩
International journal of molecular sciences (Online) 21 (2020). doi:10.3390/ijms21072635
info:cnr-pdr/source/autori:Nikolic, Ana; Jones, Takako, I; Govi, Monica; Mele, Fabiano; Maranda, Louise; Sera, Francesco; Ricci, Giulia; Ruggiero, Lucia; Vercelli, Liliana; Portaro, Simona; Villa, Luisa; Fiorillo, Chiara; Maggi, Lorenzo; Santoro, Lucio; Antonini, Giovanni; Filosto, Massimiliano; Moggio, Maurizio; Angelini, Corrado; Pegoraro, Elena; Berardinelli, Angela; Maioli, Maria Antonetta; D'Angelo, Grazia; Di Muzio, Antonino; Siciliano, Gabriele; Tomelleri, Giuliano; D'Esposito, Maurizio; Della Ragione, Floriana; Brancaccio, Arianna; Piras, Rachele; Rodolico, Carmelo; Mongini, Tiziana; Magdinier, Frederique; Salsi, Valentina; Jones, Peter L.; Tupler, Rossella/titolo:Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies/doi:10.3390%2Fijms21072635/rivista:International journal of molecular sciences (Online)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:21
Volume 21
Issue 7
International Journal of Molecular Sciences, 2020, 21 (7), pp.2635. ⟨10.3390/ijms21072635⟩
International Journal of Molecular Sciences, Vol 21, Iss 2635, p 2635 (2020)
International Journal of Molecular Sciences, MDPI, 2020, 21 (7), pp.2635. ⟨10.3390/ijms21072635⟩
International journal of molecular sciences (Online) 21 (2020). doi:10.3390/ijms21072635
info:cnr-pdr/source/autori:Nikolic, Ana; Jones, Takako, I; Govi, Monica; Mele, Fabiano; Maranda, Louise; Sera, Francesco; Ricci, Giulia; Ruggiero, Lucia; Vercelli, Liliana; Portaro, Simona; Villa, Luisa; Fiorillo, Chiara; Maggi, Lorenzo; Santoro, Lucio; Antonini, Giovanni; Filosto, Massimiliano; Moggio, Maurizio; Angelini, Corrado; Pegoraro, Elena; Berardinelli, Angela; Maioli, Maria Antonetta; D'Angelo, Grazia; Di Muzio, Antonino; Siciliano, Gabriele; Tomelleri, Giuliano; D'Esposito, Maurizio; Della Ragione, Floriana; Brancaccio, Arianna; Piras, Rachele; Rodolico, Carmelo; Mongini, Tiziana; Magdinier, Frederique; Salsi, Valentina; Jones, Peter L.; Tupler, Rossella/titolo:Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies/doi:10.3390%2Fijms21072635/rivista:International journal of molecular sciences (Online)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:21
Volume 21
Issue 7
International audience; Facioscapulohumeral muscular dystrophy (FSHD) is characterized by incomplete penetrance and intra-familial clinical variability. The disease has been associated with the genetic and epigenetic features of the D4Z4 repetitive e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d898b0b7ac859b62559bed3b8fc1e465
https://hal-amu.archives-ouvertes.fr/hal-03142878/file/ijms-21-02635.pdf
https://hal-amu.archives-ouvertes.fr/hal-03142878/file/ijms-21-02635.pdf
Autor:
Brancaccio, Arianna1 arianna.brancaccio@unitn.it, Tabarelli, Davide1, Bigica, Marco1, Baldauf, Daniel1
Publikováno v:
Scientific Reports. 5/20/2020, Vol. 10 Issue 1, p1-1. 1p.
Autor:
Brancaccio, Arianna, Palacios, Daniela
Publikováno v:
Frontiers in Aging Neuroscience; Apr2015, Vol. 7, p1-17, 17p
Publikováno v:
Journal of Personalized Medicine; Jan2022, Vol. 12 Issue 1, p59-N.PAG, 1p
Autor:
Consalvi, Silvia, Brancaccio, Arianna, Dall'Agnese, Alessandra, Puri, Pier Lorenzo, Palacios, Daniela
Publikováno v:
Nature Communications; Jan2017, Vol. 8 Issue 1, p13956, 1p
Autor:
Signaroldi, Elena, Laise, Pasquale, Cristofanon, Silvia, Brancaccio, Arianna, Reisoli, Elisa, Atashpaz, Sina, Terreni, Maria Rosa, Doglioni, Claudio, Pruneri, Giancarlo, Malatesta, Paolo, Testa, Giuseppe
Publikováno v:
Nature Communications; Feb2016, Vol. 7 Issue 2, p10753, 1p