MOGLIA, Cristina

MOGLIA, Cristina  

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 Strange Loop: Effects of emotional facial expressions impaired recognition in ALS Patients and in their Caregivers. 2012 A. Montuschi; A. Lo Presti; C. Moglia; A. Calvo; M. Lo Russo; F. Casale; M. Tamietto; A. Chiò
A cluster of ALS Cases in Sardinia due to a founder mutation of the TARDBP gene 2011 Chio' A; Borghero G; Pugliatti M; Ticca A; Calvo A; Moglia C; brunetti M; Ossola I; Marrosu M; Murru MR; Floris G; Cannas A; Parish LD; Cossu p; Abramzon Y; Johnson JO; Arepalli S; Chong S; Hernandez DG; Traynor BJ; Restagno G
A de novo missense mutation of the FUS gene in a "true" sporadic ALS case 2011 Chiò A; Calvo A; Moglia C; Ossola I; Brunetti M; Sbaiz L; Lai SL; Abramzon Y; Traynor BJ; Restagno G
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 longitudinal study on quality of life and depression in ALS patient-caregiver couples 2007 A. GAUTHIER; A. VIGNOLA; A. CALVO; E. CAVALLO; C. MOGLIA; L. SELLITTI; R. MUTANI; A. CHIO'
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 carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD 2011 Borghero G; Floris G; Cannas A; Marrosu MG; Murru MR; Costantino E; Parish LD; Pugliatti M; Ticca A; Traynor BJ; Calvo A; Cammarosano S; Moglia C; Cistaro A; Brunetti M; Restagno G; Chiò 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
A phase I-II multicenter study on G-CSF in ALS: clinical and hematological results 2009 Moglia C; Calvo A; Mora G; Caponnetto C; Siciliano G; Sabatelli M; La Bella V; Silani V; Corbo M; Mancardi GL; Tonali PA; Mutani R; Tarella C; Chio' A
A pilot trial of G-CSF in amyotrophic lateral sclerosis 2008 Chio' A; Mora G; Caponnetto C; Siciliano G; Sabatelli M; La Bella V; Silani V; Moglia C; Mancardi GL; Tonali P; Calvo A; Mutani R; Corbo M; Scime’ R; D’Onofrio G; Petrini M; Melazzini M. Gualandi F; Tarella C
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