GHIONE, ISABELLA
GHIONE, ISABELLA
Universita' degli Studi di MILANO
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG
2020 D. Villa, C. Cinnante, G. Valcamonica, G. Manenti, S. Lanfranconi, A. Colombi, I. Ghione, M.C. Saetti, M. D'Amico, S. Bonato, N. Bresolin, G.P. Comi, D. Ronchi
Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum : the first report
2020 S. Lanfranconi, I. Ghione, G. Valcamonica, S.P. Corti, S. Bonato, N. Bresolin
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant
2012 A. Bersano, M. Ranieri, A. Ciammola, C. Cinnante, S. Lanfranconi, M.T. Dotti, L. Candelise, C. Baschirotto, I. Ghione, E. Ballabio, N. Bresolin, M.T. Bassi
Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease
2011 D. Santoro, I. Colombo, I. Ghione, L. Peverelli, N. Bresolin, M. Sciacco, A. Prelle
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort
2011 S. Corti, D. Santoro, I. Ghione, C. Fenoglio, S. Ghezzi, M. Ranieri, D. Galimberti, M. Mancuso, G. Siciliano, C. Briani, L. Murri, E. Scarpini, J. Schymick, B. Traynor, N. Bresolin, G. Comi
Decline of ALS-FRS and Norris scale scores in a group of patients affected by ALS and treated with lithium
2009 D. Santoro, I. Ghione, S. Corti, M. Servida, A. Prelle, N. Bresolin, G.P. Comi
TARDPB gene mutations in 314 individuals with familial and sporadic ALS
2009 R. Del Bo, S. Ghezzi, S. Corti, M. Ranieri, D. Santoro, I. Ghione, M. Pandolfo, A. Prelle, G. Soraru`, C. Briani, M. Mancuso, G. Siciliano, C. Angelini, N. Bresolin, G.P. Comi
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS : identification of two novel mutations
2009 R. Del Bo, S. Ghezzi, S. Corti, M. Pandolfo, M. Ranieri, D. Santoro, I. Ghione, A. Prelle, V. Orsetti, M. Mancuso, G. Soraru , C. Briani, C. Angelini, G. Siciliano, N. Bresolin, G.P. Comi
Aphasic and visual aura with increased vasogenic leakage : an atypical migrainosus status
2009 S. Lanfranconi, S. Corti, A. Bersano, A. Costa, A. Prelle, M. Sciacco, N. Bresolin, I. Ghione
TARDBP genotyping in patients with Familial and sporadic ALS : identification of two novel mutations
2009 R. Del Bo, S. Corti, M. Ranieri, S. Ghezzi, D. Santoro, I. Ghione, M. Pandolfo, G. Sorarù, C. Braini, M. Mancuso, G. Siciliano, N. Bresolin, G.P. Comi
Nonconvulsive status epilepticus in a patient treated with carbamazepine
2008 I. Ghione, D. Santoro, V. Lucchini, A. Cappellari, A. Prelle, G. Conti, N. Bresolin
Parkin polymorphisms and environmental exposure: Reduction of Parkinson’s Disease age of onset XVIIth
2007 I. Ghione, A. Di Fonzo, F. Saladino, R. Del Bo, N. Bresolin, G.P. Comi, M. Rango
Parkin polymorphisms and environmental exposure : Decrease in age at onset of Parkinson's disease
2007 I. Ghione, A. Di Fonzo, F. Saladino, R. Del Bo, N. Bresolin, G.P. Comi, M. Rango
Related Articles,Links Pasrkinson's disease, chronic hygrocarbon exposure and striatal neuronal damage: a 1-H MRS study
2006 M. Rango, M. Canesi, I. Ghione, M. Farabola, A. Righini, N. Bresolin, A. Antonini, G. Pezzoli
PARK2 gene variability in idiopathic Parkinson's disease
2005 I. Ghione, M. Rango, A. Di Fonzo, R. Del Bo, F. Saladino, N. Bresolin, G.P. Comi
PARK2 gene variability in idiopathic Parkinson's disease
2005 I. Ghione, M. Rango, A. Di Fonzo, R. Del Bo, F. Saladino, N. Bresolin, G.P. Comi
PARK2 gene variability in idiopathic Parkinson’s disease
2005 A. Di Fonzo, I. Ghione, R. Del Bo, F. Saladino, M. Rango, N. Bresolin, G.P. Comi