CANOSA, Antonio

CANOSA, Antonio  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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18 F-FDG-PET correlates of cognitive impairment in ALS 2016 Canosa, Antonio; Pagani, Marco; Cistaro, Angelina; Montuschi, Anna; Iazzolino, Barbara; Fania, Piercarlo; Cammarosano, Stefania; Ilardi, Antonio; Moglia, Cristina; Calvo, Andrea; Chiò, Adriano
A de novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case. 2014 A. Calvo;C. Moglia;A. Canosa;M. Brunetti;M. Barberis;B. J. Traynor;G. Carrara;C. Valentini;G. Restagno;A. Chiò
A familial ALS case carrying a novel p.G147C SOD1 heterozygous missense mutation with non-executive cognitive impairment. 2014 A. Canosa;A. Calvo;C. Moglia;B. Iazzolino;M. Brunetti;G. Restagno;A. Cistaro;P. Fania;G. Carrara;M. C. Valentini;R. Tanel;A. Chiò
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutation 2020 Canosa A.; Grassano M.; Barberis M.; Brunetti M.; Manera U.; Vasta R.; Cammarosano S.; De Marco G.; Calvo A.; Chio A.; Moglia C.
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course. 2015 A. Canosa;A. Calvo;C. Moglia;M. Barberis;M. Brunetti;S. Cammarosano;U. Manera;A. Ilardi;G. Restagno;A. Chiò
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms 2018 Canosa A.; De Marco G.; Lomartire A.; Rinaudo M.T.; Di Cunto F.; Turco E.; Barberis M.; Brunetti M.; Casale F.; Moglia C.; Calvo A.; Marklund S.L.; Andersen P.M.; Mora G.; Chio A.
A novel splice site FUS mutation in a familial ALS case: effects on protein expression 2021 Canosa A.; Lomartire A.; De Marco G.; Grassano M.; Brunetti M.; Manera U.; Vasta R.; Salamone P.; Fuda G.; Sbaiz L.; Gallone S.; Moglia C.; Calvo A.; Chio A.
A PET/CT approach to spinal cord metabolism in amyotrophic lateral sclerosis 2016 Marini, Cecilia; Cistaro, Angelina; Campi, Cristina; Calvo, Andrea; Caponnetto, Claudia; Nobili, Flavio Mariano; Fania, Piercarlo; Beltrametti, Mauro C.; Moglia, Cristina; Novi, Giovanni; Buschiazzo, Ambra; Perasso, Annalisa; Canosa, Antonio; Scialò, Carlo; Pomposelli, Elena; Massone, Anna Maria; Bagnara, Maria Caludia; Cammarosano, Stefania; Bruzzi, Paolo; Morbelli, Silvia; Sambuceti, Gianmario; Mancardi, Gianluigi; Piana, Michele; Chio', Adriano
Acoustic reflex patterns in amyotrophic lateral sclerosis 2017 Canale, Andrea; Albera, Roberto; Lacilla, Michelangelo; Canosa, Antonio; Albera, Andrea; Sacco, Francesca; Chio', Adriano; Calvo, Andrea
Acute, Hemorrhagic, Necrotizing Pancreatitis Associated With Riluzole Treatment in a Patient With Amyotrophic Lateral Sclerosis 2022 Cabras, Sara; Calvo, Andrea; Moglia, Cristina; Chiò, Adriano; Canosa, Antonio
ALS clinical trials: Do enrolled patients accurately represent the ALS population? 2011 Chiò A; Canosa A; Gallo S; Cammarosano S; Moglia C; Fuda G; Calvo A; Mora G; For the PARALS group
ALS Clinical Trials: Do the Enrolled Patients Represent the ALS Population? 2011 Chio' A; Mora G; Moglia C; Fuda G; Canosa A; Gallo S; Cammarosano S; Ilardi A; Calvo A
ALS phenotype is influenced by age, sex, and genetics: A population-based study 2020 Chiò, Adriano; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; D'Ovidio, Fabrizio; Vasta, Rosario; Grassano, Maurizio; Brunetti, Maura; Barberis, Marco; Corrado, Lucia; D'Alfonso, Sandra; Iazzolino, Barbara; Peotta, Laura; Sarnelli, Maria Francesca; Solara, Valentina; Zucchetti, Jean Pierre; De Marchi, Fabiola; Mazzini, Letizia; Mora, Gabriele; Calvo, Andrea
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations 2012 Chio' A; Restagno G; Brunetti M; Ossola I; Calvo A; Canosa A; Moglia C; Floris G; Tacconi P; Marrosu F; Marrosu MG; Murru MR; Majounie E; Renton AE; Abramzon Y; Pugliatti M; Sotgiu MA; Traynor BJ; Borghero G
Amyotrophic lateral sclerosis caregiver burden and patients’ quality of life during COVID-19 pandemic 2021 Giusiano S.; Peotta L.; Iazzolino B.; Mastro E.; Arcari M.; Palumbo F.; Torrieri M.C.; Bombaci A.; Grassano M.; Cabras S.; Di Pede F.; De Mattei F.; Matteoni E.; Solero L.; Daviddi M.; Salamone P.; Fuda G.; Manera U.; Canosa A.; Chio A.; Calvo A.; Moglia C.; Vasta R.
Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor. 2015 A. Canosa;A. Calvo;M. Barberis;M. Brunetti;G. Restagno;S. Cammarosano;A. Ilardi;M. C. Vigliani;A. Chiò;C. Moglia
Amyotrophic lateral sclerosis outcome measures and the role of albumin and creatinine: a population-based study 2014 A. Chiò;A. Calvo;G. Bovio;A. Canosa;D. Bertuzzo;F. Galmozzi;P. Cugnasco;M. Clerico;S. De Mercanti;E. Bersano;S. Cammarosano;A. Ilardi;U. Manera;C. Moglia;R. Sideri;K. Marinou;E. Bottacchi;F. Pisano;R. Cantello;L. Mazzini;G. Mora; Piemonte;V. d. Register
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes 2022 Canosa A.; Calvo A.; Moglia C.; Vasta R.; Palumbo F.; Solero L.; Di Pede F.; Cabras S.; Arena V.; Zocco G.; Casale F.; Brunetti M.; Sbaiz L.; Gallone S.; Grassano M.; Manera U.; Pagani M.; Chio A.
Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene 2012 Calvo A; Moglia C; Canosa A; Cistaro A; Valentini C; Carrara G; Soldano E; Ilardi A; Bersano E; Bertuzzo D; Brunetti M; Ossola I; Restagno G; Chio' A
An ALS case with a novel D90N-SOD1 heterozygous missense mutation 2012 Calvo A; Ilardi A; Moglia C; Canosa A; Carrara G; Valentini C; Ossola I; Brunetti M; Restagno G; Chio' A