SANTORO, DOMENICO
SANTORO, DOMENICO
Universita' degli Studi di MILANO
Opsoclonus-myoclonus syndrome associated with human herpes virus-6 rhomboencephalitis
2014 V. Belcastro, M. Piola, S. Binda, D. Santoro, M. Rezzonico, M. Arnaboldi
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
Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease
2011 D. Santoro, I. Colombo, I. Ghione, L. Peverelli, N. Bresolin, M. Sciacco, A. Prelle
Contribution of FUS gene to FTLD-ALS spectrum: a genetic study in an Italian color of 484 patients
2010 R. Del Bo, S. Corti, S. Archetti, A. Papetti, G. Riboldi, S. Ghezzi, M. Ranieri, D. Santoro, A. Padovani, N. Bresolin, G.P. Comi, B. Borroni
Guillain-Barre syndrome after rtPA therapy for acute stroke
2010 A. Bersano, D. Santoro, A. Prelle, S. Lanfranconi, M. Ranieri, C. Tadeo, N. Bresolin, P. Baron
Progranulin genotyping in 237 sporadic amyotrophic lateral sclerosis patients
2009 R. Del Bo, S. Ghezzi, S. Corti, D. Santoro, C. Briani, M. Mancuso, G. Siciliano, C. Fenoglio, D. Galimberti, E. Scarpini, N. Bresolin, G.P. 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
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
2009 R. Virgilio, S.P. Corti, P. Agazzi, D. Santoro, S. Lanfranconi, L. Candelise, N. Bresolin, G.P. Comi, A. Bersano
Progranulin genotyping in 237 sporadic amyothropic lateral sclerosis patients
2009 R. DEL BO, S. Ghezzi, S. Corti, D. Santoro, C. Briani, M. Mancuso, G. Siciliano, C. Fenoglio, D. Galimberti, E. Scarpini, N. Bresolin, G. Comi
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
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
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction
2009 S. Corti, C. Donadoni, D. Ronchi, A. Bordoni, F. Fortunato, D. Santoro, R. Del Bo, V. Lucchini, V. Crugnola, D. Papadimitriou, S. Salani, M. Moggio, 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
Progranulin genetic variability is not associated to sporadic amyotrophic lateral sclerosis in Italian patients
2008 D. Santoro, S. Ghezzi, S. Corti, M.E. Fruguglietti, A. Prelle, M. Mancuso, G. Siciliano, C. Briani, N. Bresolin, G.P. Comi, R. DEL BO
Glicogenosi di tipo III: rivalutazione delle caratteristiche cliniche e genetiche dei pazienti e stato dell’arte sul modello murino knock-out.
2008 G.P. Comi, S. Lucchiari, S. Pagliarani, D. Santoro
Absence of angiogenic genes modification in Italian ALS patients.
2008 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, S. Corti, F. Locatelli, D. Santoro, A. Prelle, C. Briani, M. Nardini, G. Siciliano, M. Mancuso, L. Murri, N. Bresolin, G.P. Comi
Progranulin genetic variability is not associated to sporadic Amyotrophic Lateral Sclerosis in Italian petients.
2008 S. Ghezzi, S. Corti, D. Santoro, C. Briani, M. Mancuso, G. Siciliano, N. Bresolin, G.P. Comi, R. Del Bo
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients
2008 R. Del Bo, S. Ghezzi, S. Corti, D. Santoro, A. Prelle, M. Mancuso, G. Siciliano, C. Briani, L. Murri, N. Bresolin, G.P. Comi
Disease natural history in a large group of genetically diagnosed glycogen storage disease type III.
2007 D. Santoro, S. Lucchiari, S. Pagliarani, A. Bordoni, M. Filocamo, M. Di Rocco, C. Rodolico, A. Toscano, D. Melis, R. Parini, S. Paci, M. Giovannini, M. Donati, N. Bresolin, G.P. Comi