Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Gianfranco Carrara"'
Autor:
Alessia Nasca, Teresa Rizza, Mara Doimo, Andrea Legati, Andrea Ciolfi, Daria Diodato, Cristina Calderan, Gianfranco Carrara, Eleonora Lamantea, Chiara Aiello, Michela Di Nottia, Marcello Niceta, Costanza Lamperti, Anna Ardissone, Stefania Bianchi-Marzoli, Giancarlo Iarossi, Enrico Bertini, Isabella Moroni, Marco Tartaglia, Leonardo Salviati, Rosalba Carrozzo, Daniele Ghezzi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Abstract Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring compound heterozygous OPA1 mutations have been described manifesting
Externí odkaz:
https://doaj.org/article/0494d6719b26407982a6465aec056ef3
Autor:
Gianfranco Carrara
Publikováno v:
Techne, Iss 13 (2017)
Externí odkaz:
https://doaj.org/article/c1591934d22e4c65863efc059bcde2fe
Autor:
Gianfranco, Carrara, Nicoletta, Dubini, Tiziana, Ferrante, Monica, Ingaglio, Maurizio, Mauri, Federica Meoli (Segreteria tecnica, e organizzativa), Roberto, Palumbo, Peretti, Gabriella, Pollo, Riccardo, Roberto Ravegnani Morosini, Raffaella, Scorziello, Marco, Vitali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2153::2cf9b06ee7fdeb0e2016af5bca69c0a4
http://hdl.handle.net/11583/2724328
http://hdl.handle.net/11583/2724328
Autor:
Giancarlo Iarossi, Enrico Bertini, Andrea Ciolfi, Isabella Moroni, Daniele Ghezzi, Daria Diodato, Costanza Lamperti, Teresa Rizza, Rosalba Carrozzo, Cristina Calderan, Eleonora Lamantea, Stefania Bianchi-Marzoli, Andrea Legati, Michela Di Nottia, Marco Tartaglia, Alessia Nasca, Marcello Niceta, Gianfranco Carrara, Chiara Aiello, Anna Ardissone, Mara Doimo, Leonardo Salviati
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Background Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring compound heterozygous OPA1 mutations have been described manifesting complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb957555401e93ed052e07402f417070
http://hdl.handle.net/10281/205499
http://hdl.handle.net/10281/205499
Autor:
Gianfranco, Carrara, Nicoletta, Dubini, Tiziana, Ferrante, Monica, Ingaglio, Maurizio, Mauri, Federica, Meoli, Roberto, Palumbo, Peretti, Gabriella, Pollo, Riccardo, Roberto Ravegnani Morosini, Raffaella, Scorziello, Marco, Vitali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2153::570064be73abcb11d521345033a858d9
http://hdl.handle.net/11583/2724331
http://hdl.handle.net/11583/2724331
Gli Atti del VI Congresso Internazionale dell'Ar.Tec. sono in qualche modo rifondativi del settore; hanno riguardato le ricerche svolte in questo settore scientificodisciplinare per farne una panoramica dello stato dell'arte in Italia, un confronto c
Publikováno v:
Proceedings of the 34th Annual Conference of the Association for Computer Aided Design in Architecture (ACADIA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ad6b3df6eda676e57c7884e6766f86
https://doi.org/10.52842/conf.acadia.2014.681
https://doi.org/10.52842/conf.acadia.2014.681
Autor:
Graziella Uziel, Eleonora Lamantea, Gianfranco Carrara, Carlo Antozzi, Silvana Franceschetti, Massimo Zeviani, Laura Canafoglia
Publikováno v:
Novel Aspects on Epilepsy
Mitochondrial encephalopathies (MEs) are characterized by an extreme clinical heterogeneity since they can involve different systems and manifest at distinct ages with variable course. Many affected individuals display a cluster of clinical features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a684814eed08202fb36424b100b952f
https://doi.org/10.5772/22014
https://doi.org/10.5772/22014