Sfoglia per Autore
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
Novel SOD1 Q23R mutation associated with muscle mitochondrial dysfunction in familial ALS International Meeting “Mutant SOD1 and familial ALS: from the molecule to man
2007 S. Corti, A. Bordoni, D. Ronchi, D. Santoro, S. Salani, C. Donadoni, C. Lamperti, V. Lucchini, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Absence of association between erythropoietin gene variation and ALS in sporadic Italian patients.
2007 S. Ghezzi, R. Del Bo, S. Corti, D. Santoro, A. Prelle, M. Nardini, G. Siciliano, M. Mancuso, L. Murri, N. Bresolin, G.P. Comi
Novel Q23R SOD1 mutation associated with muscle mitochondrial dysfunction
2007 D. Ronchi, S. Corti, A. Bordoni, D. Santoro, D. Papadimitriou, C. Lamperti, V. Lucchini, M. Magri, M. Guglieri, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis
2007 V. Crugnola, V. Lucchini, S. Corti, L. Adobbati, A. Ciammola, N. Ticozzi, M.E. Fruguglietti, A. Prelle, D. Santoro, R. Virgilio, V. Silani, N. Bresolin, M. Moggio, G.P. Comi
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction
2007 S. Corti, A. Bordoni, D. Ronchi, D. Santoro, D. Papadimitriou, C. Lamperti, V. Lucchini, F. Magri, M. Guglieri, V. Crugnola, 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
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
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
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
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
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
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
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
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
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
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