CANOSA, Antonio
CANOSA, Antonio
NEUROSCIENZE "RITA LEVI MONTALCINI"
18 F-FDG-PET correlates of cognitive impairment in ALS
2016-01-01 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.
2014-01-01 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.
2014-01-01 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
2020-01-01 Canosa A.; Grassano M.; Barberis M.; Brunetti M.; Manera U.; Vasta R.; Cammarosano S.; De Marco G.; Calvo A.; Chio A.; Moglia C.
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease
2024-01-01 Canosa, Antonio; Cabras, Sara; Di Pede, Francesca; Manera, Umberto; Vasta, Rosario; Moglia, Cristina; Calvo, Andrea; Gallone, Salvatore; Chiò, Adriano
A novel DHTKD1 variant is associated with an atypical form of Charcot-Marie-Tooth disease type 2Q?
2024-01-01 Matteoni, E; Canosa, A; Chiò, A; Moglia, C; Gallone, S
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course.
2015-01-01 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
2018-01-01 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
2021-01-01 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 patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene
2023-01-01 Parisi, Mattia; Canosa, Antonio; Tessa, Alessandra; Ferrero, Bruno; Gallone, Salvatore
A PET/CT approach to spinal cord metabolism in amyotrophic lateral sclerosis
2016-01-01 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
2017-01-01 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
2022-01-01 Cabras, Sara; Calvo, Andrea; Moglia, Cristina; Chiò, Adriano; Canosa, Antonio
Adult-onset spastic paraplegia associated with a novel SPTBN2 missense heterozygous variant
2024-01-01 Palumbo, Francesca; Canosa, Antonio; Moglia, Cristina; Calvo, Andrea; Gallone, Salvatore
ALS clinical trials: Do enrolled patients accurately represent the ALS population?
2011-01-01 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?
2011-01-01 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
2020-01-01 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
2012-01-01 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
2022-01-01 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.
2015-01-01 A. Canosa;A. Calvo;M. Barberis;M. Brunetti;G. Restagno;S. Cammarosano;A. Ilardi;M. C. Vigliani;A. Chiò;C. Moglia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease | 2024 | Canosa, Antonio; Cabras, Sara; Di Pede, Francesca; Manera, Umberto; Vasta, Rosario; Moglia, Cristina; Calvo, Andrea; Gallone, Salvatore; Chiò, Adriano | |
| A novel DHTKD1 variant is associated with an atypical form of Charcot-Marie-Tooth disease type 2Q? | 2024 | Matteoni, E; Canosa, A; Chiò, A; Moglia, C; Gallone, S | |
| 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 patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene | 2023 | Parisi, Mattia; Canosa, Antonio; Tessa, Alessandra; Ferrero, Bruno; Gallone, Salvatore | |
| 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 | |
| Adult-onset spastic paraplegia associated with a novel SPTBN2 missense heterozygous variant | 2024 | Palumbo, Francesca; Canosa, Antonio; Moglia, Cristina; Calvo, Andrea; Gallone, Salvatore | |
| 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 | 2022 | 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 |