Sfoglia per Autore
Multiple memory-guided saccades: movement memory improves the accuracy of memory-guided saccades
2008-01-01 Colnaghi, Silvia; Beltrami, Giorgio; Cortese, Andrea; Zangemeister, Wh; Cosi, Vittorio; Versino, Maurizio
Varicella zoster virus-associated polyradiculoneuritis
2009-01-01 Cortese, A; Tavazzi, E; Delbue, S; Alfonsi, E; Pichiecchio, A; Ceroni, Mauro; Ferrante, P; Marchioni, E.
Theta burst stimulation of the cerebellum impairs motor learning in humans.
2010-01-01 Colnaghi, Silvia; Ramat, Stefano; D'Angelo, EGIDIO UGO; Cortese, Andrea; Beltrami, Giorgio; Moglia, Arrigo; Versino, Maurizio
Theta-Burst Stimulation of the Cerebellum Interferes with Internal Representations of Sensory-Motor Information Related to Eye Movements in Humans
2011-01-01 Colnaghi, Silvia; Ramat, Stefano; D'Angelo, EGIDIO UGO; Cortese, Andrea; Beltrami, Giorgio; Moglia, Arrigo; Versino, Maurizio
Late onset oculopharyngeal muscular dystrophy with prominent neurogenic features and short GCG trinucleotide expansion
2011-01-01 Piccolo, G.; Cortese, A.; Tavazzi, E.; Piccolo, L.; Sassone, J.; Ciammola, A.; Alfonsi, E.; Colombo, I.; Moggio, M.
Monitoring late complications of zinc treatment in Wilson's disease. Reply to the letter: Copper deficiency in Wilson's disease: An avoidable complication of treatment: Monitoring Late Complications of Zinc Treatment in Wilson's Disease
2011-01-01 Cortese, A.; Zangaglia, R.; Lozza, A.; Piccolo, G.; Pacchetti, C.
Copper deficiency in Wilson's disease: Peripheral neuropathy and myelodysplastic syndrome complicating zinc treatment
2011-01-01 Cortese, A.; Zangaglia, R.; Lozza, A.; Piccolo, G.; Pacchetti, C.
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study
2012-01-01 Obici, L; Cortese, A; Lozza, A; Lucchetti, J; Gobbi, M; Palladini, Giovanni; Perlini, Stefano; Saraiva, Mj; Merlini, Giampaolo
Guillain-Barré syndrome associated with the D222E variant of the 2009 pandemic influenza A (H1N1) virus: Case report and review of the literature
2012-01-01 Cortese, A.; Baldanti, F.; Tavazzi, E.; Carnevale, L.; Minoli, L.; Lozza, A.; Marchioni, E.
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial.
2013-01-01 Berk, Jl; Suhr, Ob; Obici, L; Sekijima, Y; Zeldenrust, Sr; Yamashita, T; Heneghan, Ma; Gorevic, Pd; Litchy, Wj; Wiesman, Jf; Nordh, E; Corato, M; Lozza, A; Cortese, A; Robinson Papp, J; Colton, T; Rybin, Dv; Bisbee, Ab; Ando, Y; Ikeda, S; Seldin, Dc; Merlini, Giampaolo; Skinner, M; Kelly, Jw; Dyck, Pj; Diflunisal Trial ConsortiumBerk, Jl1; Suhr, Ob2; Obici, L3; Sekijima, Y4; Zeldenrust, Sr5; Yamashita, T6; Heneghan, Ma7; Gorevic, Pd8; Litchy, Wj5; Wiesman, Jf1; Nordh, E2; Corato, M9; Lozza, A10; Cortese, A10; Robinson Papp, J8; Colton, T11; Rybin, Dv12; Bisbee, Ab12; Ando, Y6; Ikeda, S4; Seldin, Dc1; Merlini, G3; Skinner, M1; Kelly, Jw13; Dyck, Pj5; Collaborators Falk RH, Diflunisal Trial C. o. n. s. o. r. t. i. u. m.; Miller FA, Jr; Horibata, Y; Koyama, J; Morita, H; Perlini, Stefano; Lindqvist, P; Davies, J; Heldestad, V; Frykolm, C; Lundgren, He; Lodermeier, K; Orr, P; Thompson, M.
Repurposing diflunisal for familial amyloid polyneuropathy: A randomized clinical trial
2013-01-01 Berk, John L; Suhr, Ole B.; Obici, Laura; Sekijima, Yoshiki; Zeldenrust, Steven R.; Yamashita, Taro; Heneghan, Michael A.; Gorevic, Peter D.; Litchy, William J.; Wiesman, Janice F.; Nordh, Erik; Corato, Manuel; Lozza, Alessandro; Cortese, Andrea; Robinson Papp, Jessica; Colton, Theodore; Rybin, Denis V.; Bisbee, Alice B.; Ando, Yukio; Ikeda, Shu Ichi; Seldin, David C.; Merlini, Giampaolo; Skinner, Martha; Kelly, Jeffery W.; Dyck, Peter J.
Graphical modelling of molecular networks underlying sporadic inclusion body myositis
2013-01-01 Thorne, T.; Fratta, P.; Hanna, M. G.; Cortese, A.; Plagnol, V.; Fisher, E. M.; Stumpf, M. P. H.
Longitudinal observational study of sporadic inclusion body myositis: Implications for clinical trials
2013-01-01 Cortese, A.; Machado, P.; Morrow, J.; Dewar, L.; Hiscock, A.; Miller, A.; Brady, S.; Hilton-Jones, D.; Parton, M.; Hanna, M. G.
Novel CLN3 mutation causing autophagic vacuolar myopathy.
2014-01-01 Cortese, A1; Tucci, A2; Piccolo, G2; Galimberti, Ca2; Fratta, P2; Marchioni, E2; Grampa, G2; Cereda, C2; Grieco, G2; Ricca, I2; Pittman, A2; Ciscato, P2; Napoli, L2; Lucchini, V2; Ripolone, M2; Violano, R2; Fagiolari, G2; Mole, Se2; Hardy, J2; Moglia, Arrigo; Moggio, M. 2.
Correlation of clinical and molecular features in spinal bulbar muscular atrophy
2014-01-01 Fratta, P.; Nirmalananthan, N.; Masset, L.; Skorupinska, I.; Collins, T.; Cortese, A.; Pemble, S.; Malaspina, A.; Fisher, E. M. C.; Greensmith, L.; Hanna, M. G.
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis
2014-01-01 Corrochano, S.; Mannikko, R.; Joyce, P. I.; Mcgoldrick, P.; Wettstein, J.; Lassi, G.; Rayan, D. L. R.; Blanco, G.; Quinn, C.; Liavas, A.; Lionikas, A.; Amior, N.; Dick, J.; Healy, E. G.; Stewart, M.; Carter, S.; Hutchinson, M.; Bentley, L.; Fratta, P.; Cortese, A.; Cox, R.; Steve, D.; Tucci, V.; Wackerhage, H.; Amato, A. A.; Greensmith, L.; Koltzenburg, M.; Hanna, M. G.; Acevedo-Arozena, A.
Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy
2014-01-01 Cortese, A.; Plagnol, V.; Brady, S.; Simone, R.; Lashley, T.; Acevedo-Arozena, A.; De Silva, R.; Greensmith, L.; Holton, J.; Hanna, M. G.; Fisher, E. M. C.; Fratta, P.
Novel CLN3 mutation causing autophagic vacuolar myopathy
2014-01-01 Cortese, Andrea; Tucci, Arianna; Piccolo, Giovanni; Galimberti, Carlo A; Fratta, Pietro; Marchioni, Enrico; Grampa, Gianpiero; Cereda, Cristina; Grieco, Gaetano; Ricca, Ivana; Pittman, Alan; Ciscato, Patrizia; Napoli, Laura; Lucchini, Valeria; Ripolone, Michela; Violano, Raffaella; Fagiolari, Gigliola; Mole, Sara E; Hardy, John; Moglia, Arrigo; Moggio, Maurizio
CLINICAL FEATURES AND SEROLOGICAL PROFILE OF COMBINED CENTRAL AND PERIPHERAL DEMYELINATION
2015-01-01 By:cortese, A[ 1 ]; Alfonsi, E[ 1 ]; Devaux, J[ 2 ]; Franciotta, D[ 1 ]; Manso, C[ 2 ]; Visigalli, N[ 1 ]; Zardini, E[ 1 ]; Diamanti, L[ 1 ]; Prunetti, P[ 1 ]; Osera, C[ 1 ]; Osera, Cecilia; M[, 3; 4, ]; Berzero, G[ 1 ]; Pichiecchio, A[ 1 ]; Piccolo, G[ 1 ]; Lozza, A[ 1 ]; Piscosquito, G[ 5 ]; Salsano, E[ 5 ]; Ceroni, Mauro; Moglia, A[ 1 ]; Bono, ; G[, 3; 4, ]; Pareyson, D[ 5 ]; Marchioni, E.
Ambient air pollution boosts MS activity through upregulation of adhesion molecules and chemokine receptors on circulating lymphocytes
2015-01-01 Cortese, A; Lova, L; Villa, S; La Salvia, S; Nosari, G; Romani, A; Franciotta, D; GIGLI BERZOLARI, Francesca; Borrelli, Paola; Cereda, C; Bergamaschi, R.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Multiple memory-guided saccades: movement memory improves the accuracy of memory-guided saccades | 1-gen-2008 | Colnaghi, Silvia; Beltrami, Giorgio; Cortese, Andrea; Zangemeister, Wh; Cosi, Vittorio; Versino, Maurizio | |
Varicella zoster virus-associated polyradiculoneuritis | 1-gen-2009 | Cortese, A; Tavazzi, E; Delbue, S; Alfonsi, E; Pichiecchio, A; Ceroni, Mauro; Ferrante, P; Marchioni, E. | |
Theta burst stimulation of the cerebellum impairs motor learning in humans. | 1-gen-2010 | Colnaghi, Silvia; Ramat, Stefano; D'Angelo, EGIDIO UGO; Cortese, Andrea; Beltrami, Giorgio; Moglia, Arrigo; Versino, Maurizio | |
Theta-Burst Stimulation of the Cerebellum Interferes with Internal Representations of Sensory-Motor Information Related to Eye Movements in Humans | 1-gen-2011 | Colnaghi, Silvia; Ramat, Stefano; D'Angelo, EGIDIO UGO; Cortese, Andrea; Beltrami, Giorgio; Moglia, Arrigo; Versino, Maurizio | |
Late onset oculopharyngeal muscular dystrophy with prominent neurogenic features and short GCG trinucleotide expansion | 1-gen-2011 | Piccolo, G.; Cortese, A.; Tavazzi, E.; Piccolo, L.; Sassone, J.; Ciammola, A.; Alfonsi, E.; Colombo, I.; Moggio, M. | |
Monitoring late complications of zinc treatment in Wilson's disease. Reply to the letter: Copper deficiency in Wilson's disease: An avoidable complication of treatment: Monitoring Late Complications of Zinc Treatment in Wilson's Disease | 1-gen-2011 | Cortese, A.; Zangaglia, R.; Lozza, A.; Piccolo, G.; Pacchetti, C. | |
Copper deficiency in Wilson's disease: Peripheral neuropathy and myelodysplastic syndrome complicating zinc treatment | 1-gen-2011 | Cortese, A.; Zangaglia, R.; Lozza, A.; Piccolo, G.; Pacchetti, C. | |
Doxycycline plus tauroursodeoxycholic acid for transthyretin amyloidosis: a phase II study | 1-gen-2012 | Obici, L; Cortese, A; Lozza, A; Lucchetti, J; Gobbi, M; Palladini, Giovanni; Perlini, Stefano; Saraiva, Mj; Merlini, Giampaolo | |
Guillain-Barré syndrome associated with the D222E variant of the 2009 pandemic influenza A (H1N1) virus: Case report and review of the literature | 1-gen-2012 | Cortese, A.; Baldanti, F.; Tavazzi, E.; Carnevale, L.; Minoli, L.; Lozza, A.; Marchioni, E. | |
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. | 1-gen-2013 | Berk, Jl; Suhr, Ob; Obici, L; Sekijima, Y; Zeldenrust, Sr; Yamashita, T; Heneghan, Ma; Gorevic, Pd; Litchy, Wj; Wiesman, Jf; Nordh, E; Corato, M; Lozza, A; Cortese, A; Robinson Papp, J; Colton, T; Rybin, Dv; Bisbee, Ab; Ando, Y; Ikeda, S; Seldin, Dc; Merlini, Giampaolo; Skinner, M; Kelly, Jw; Dyck, Pj; Diflunisal Trial ConsortiumBerk, Jl1; Suhr, Ob2; Obici, L3; Sekijima, Y4; Zeldenrust, Sr5; Yamashita, T6; Heneghan, Ma7; Gorevic, Pd8; Litchy, Wj5; Wiesman, Jf1; Nordh, E2; Corato, M9; Lozza, A10; Cortese, A10; Robinson Papp, J8; Colton, T11; Rybin, Dv12; Bisbee, Ab12; Ando, Y6; Ikeda, S4; Seldin, Dc1; Merlini, G3; Skinner, M1; Kelly, Jw13; Dyck, Pj5; Collaborators Falk RH, Diflunisal Trial C. o. n. s. o. r. t. i. u. m.; Miller FA, Jr; Horibata, Y; Koyama, J; Morita, H; Perlini, Stefano; Lindqvist, P; Davies, J; Heldestad, V; Frykolm, C; Lundgren, He; Lodermeier, K; Orr, P; Thompson, M. | |
Repurposing diflunisal for familial amyloid polyneuropathy: A randomized clinical trial | 1-gen-2013 | Berk, John L; Suhr, Ole B.; Obici, Laura; Sekijima, Yoshiki; Zeldenrust, Steven R.; Yamashita, Taro; Heneghan, Michael A.; Gorevic, Peter D.; Litchy, William J.; Wiesman, Janice F.; Nordh, Erik; Corato, Manuel; Lozza, Alessandro; Cortese, Andrea; Robinson Papp, Jessica; Colton, Theodore; Rybin, Denis V.; Bisbee, Alice B.; Ando, Yukio; Ikeda, Shu Ichi; Seldin, David C.; Merlini, Giampaolo; Skinner, Martha; Kelly, Jeffery W.; Dyck, Peter J. | |
Graphical modelling of molecular networks underlying sporadic inclusion body myositis | 1-gen-2013 | Thorne, T.; Fratta, P.; Hanna, M. G.; Cortese, A.; Plagnol, V.; Fisher, E. M.; Stumpf, M. P. H. | |
Longitudinal observational study of sporadic inclusion body myositis: Implications for clinical trials | 1-gen-2013 | Cortese, A.; Machado, P.; Morrow, J.; Dewar, L.; Hiscock, A.; Miller, A.; Brady, S.; Hilton-Jones, D.; Parton, M.; Hanna, M. G. | |
Novel CLN3 mutation causing autophagic vacuolar myopathy. | 1-gen-2014 | Cortese, A1; Tucci, A2; Piccolo, G2; Galimberti, Ca2; Fratta, P2; Marchioni, E2; Grampa, G2; Cereda, C2; Grieco, G2; Ricca, I2; Pittman, A2; Ciscato, P2; Napoli, L2; Lucchini, V2; Ripolone, M2; Violano, R2; Fagiolari, G2; Mole, Se2; Hardy, J2; Moglia, Arrigo; Moggio, M. 2. | |
Correlation of clinical and molecular features in spinal bulbar muscular atrophy | 1-gen-2014 | Fratta, P.; Nirmalananthan, N.; Masset, L.; Skorupinska, I.; Collins, T.; Cortese, A.; Pemble, S.; Malaspina, A.; Fisher, E. M. C.; Greensmith, L.; Hanna, M. G. | |
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis | 1-gen-2014 | Corrochano, S.; Mannikko, R.; Joyce, P. I.; Mcgoldrick, P.; Wettstein, J.; Lassi, G.; Rayan, D. L. R.; Blanco, G.; Quinn, C.; Liavas, A.; Lionikas, A.; Amior, N.; Dick, J.; Healy, E. G.; Stewart, M.; Carter, S.; Hutchinson, M.; Bentley, L.; Fratta, P.; Cortese, A.; Cox, R.; Steve, D.; Tucci, V.; Wackerhage, H.; Amato, A. A.; Greensmith, L.; Koltzenburg, M.; Hanna, M. G.; Acevedo-Arozena, A. | |
Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy | 1-gen-2014 | Cortese, A.; Plagnol, V.; Brady, S.; Simone, R.; Lashley, T.; Acevedo-Arozena, A.; De Silva, R.; Greensmith, L.; Holton, J.; Hanna, M. G.; Fisher, E. M. C.; Fratta, P. | |
Novel CLN3 mutation causing autophagic vacuolar myopathy | 1-gen-2014 | Cortese, Andrea; Tucci, Arianna; Piccolo, Giovanni; Galimberti, Carlo A; Fratta, Pietro; Marchioni, Enrico; Grampa, Gianpiero; Cereda, Cristina; Grieco, Gaetano; Ricca, Ivana; Pittman, Alan; Ciscato, Patrizia; Napoli, Laura; Lucchini, Valeria; Ripolone, Michela; Violano, Raffaella; Fagiolari, Gigliola; Mole, Sara E; Hardy, John; Moglia, Arrigo; Moggio, Maurizio | |
CLINICAL FEATURES AND SEROLOGICAL PROFILE OF COMBINED CENTRAL AND PERIPHERAL DEMYELINATION | 1-gen-2015 | By:cortese, A[ 1 ]; Alfonsi, E[ 1 ]; Devaux, J[ 2 ]; Franciotta, D[ 1 ]; Manso, C[ 2 ]; Visigalli, N[ 1 ]; Zardini, E[ 1 ]; Diamanti, L[ 1 ]; Prunetti, P[ 1 ]; Osera, C[ 1 ]; Osera, Cecilia; M[, 3; 4, ]; Berzero, G[ 1 ]; Pichiecchio, A[ 1 ]; Piccolo, G[ 1 ]; Lozza, A[ 1 ]; Piscosquito, G[ 5 ]; Salsano, E[ 5 ]; Ceroni, Mauro; Moglia, A[ 1 ]; Bono, ; G[, 3; 4, ]; Pareyson, D[ 5 ]; Marchioni, E. | |
Ambient air pollution boosts MS activity through upregulation of adhesion molecules and chemokine receptors on circulating lymphocytes | 1-gen-2015 | Cortese, A; Lova, L; Villa, S; La Salvia, S; Nosari, G; Romani, A; Franciotta, D; GIGLI BERZOLARI, Francesca; Borrelli, Paola; Cereda, C; Bergamaschi, R. |
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