Sfoglia per Autore
Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24
2002 M.R. Winawer, F. Martinelli Boneschi, C. Barker-Cummings, J.H. Lee, J. Liu, C. Mekios, T.C. Gilliam, T.A. Pedley, W.A. Hauser, R. Ottman
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
2002 S. Kalachikov, O. Evgrafov, B. Ross, M. Winawer, C. Barker-Cummings, F.M. Boneschi, C. Choi, P. Morozov, K. Das, E. Teplitskaya, Y. Andrew, E. Cayanis, G. Penchaszadeh, A.H. Kottmann, T.A. Pedley, W.A. Hauser, R. Ottman, T.C. Gilliam
Ceramide levels are inversely associated with malignant progression of human glial tumors
2002 L. Riboni, R. Campanella, R. Bassi, R.M. Villani, S.M. Gaini, F. Martinelli-Boneschi, P. Viani, G. Tettamanti
Association between VEGF gene and sporadic Alzheimer’s Disease
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer's disease.
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
VEGF is a novel susceptibility gene for sporadic Alzheimer's disease
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Haplotype analysis in VEGF gene and increased risk of Alzheimer's disease : reply
2005 R. Del Bo, M. Scarlato, F. Martinelli Boneschi, S. Ghezzi, N. Bresolin, G.P. Comi
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families
2006 P. Striano, M. Lispi, E. Gennaro, F. Madia, M. Traverso, L. Bordo, P. Aridon, F. Martinelli Boneschi, B. Barone, B. dalla Bernardina, A. Bianchi, G. Capovilla, P. De Marco, O. Dulac, R. Gaggero, A. Gambardella, R. Nabbout, J. Prud'Homme, R. Day, F. Vanadia, M. Vecchi, P. Veggiotti, F. Vigevano, M. Viri, C. Minetti, F. Zara
Is M129V of PRNP gene associated with Alzheimer's disease? : a case-control study and a meta-analysis
2006 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, G. Galimberti, S. Galbiati, R. Virgilio, D. Galimberti, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Temozolomide in glioblastoma : results of administration at first relapse and in newly diagnosed cases. Is still proposable an alternative schedule to concomitant protocol?
2007 M. Caroli, M. Locatelli, R. Campanella, F. Motta, A. Mora, F. Prada, S. Borsa, F. Martinelli-Boneschi, A. Saladino, S.M. Gaini
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
A pilot trial of low-dose naltrexone in primary progressive multiple sclerosis
2008 M. Gironi, F. Martinelli-Boneschi, P.G. Sacerdote, C. Solaro, M. Zaffaroni, R. Cavarretta, L. Moiola, S. Bucello, M. Radaelli, V. Pilato, M. Rodegher, M. Cursi, S. Franchi, V. Martinelli, R. Nemni, G. Comi, G. Martino
HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy
2008 M. Gironi, F.R. Guerini, E. Beghi, G. Antonini, F. Martinelli-Boneschi, L. Ceresa, S. Morino, C. Agliardi, P. Ferrante, R. Nemni
GRN variability contributes to sporadic frontotemporal lobar degeneration
2009 D. Galimberti, C. Fenoglio, F. Cortini, M. Serpente, E. Venturelli, C. Villa, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, D. Scalabrini, I. Restelli, F. Martinelli Boneschi, S. Cappa, G. Binetti, C. Mariani, I. Rainero, M. Giordana, N. Bresolin, E. Scarpini
Progranulin gene variability in patients with primary progressive multiple sclerosis
2009 D. Galimberti, F. Martinelli Boneschi, C. Fenoglio, D. Scalabrini, F. Esposito, M. De Riz, L. Piccio, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Leone, G. Comi, N. Bresolin, A. Cross, E. Scarpini
Progranulin genetic variability in primary progressive multiple sclerosis
2009 C. Fenoglio, F. Esposito, D. Galimberti, D. Scalabrini, V. Martinelli, M.E. Rodegher, M. De Riz, L. Piccio, C. Comi, E. Venturelli, F. Cortini, C. Villa, N. Bresolin, A. Cross, G. Comi, E. Scarpini, F. Martinelli-Boneschi
Progranulin gene variability in a population of 239 patients with primary progressive multiple sclerosis
2009 C. Fenoglio, F. Martinelli Boneschi, D. Galimberti, D. Scalabrini, F. Esposito, M. De Riz, L.M. Piccio, R. Naismith, B.J. Parks, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, F. Monaco, N. Bresolin, A.H. Cross, E. Scarpini
Progranulin genetic variability in primary progressive multiple sclerosis
2009 C. Fenoglio, D. Galimberti, F. Martinelli-Boneschi, D. Scalabrini, F. Esposito, M. De Riz, L. Piccio, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Leone, N. Bresolin, A. Cross, G. Comi, E. Scarpini
Progranulin genetic variability in primary progressive multiple sclerosis.
2009 C. Fenoglio, D. Galimberti, F. Martinelli-Boneschi, D. Scalabrini, F. Esposito, M. De Riz, L. Piccio, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Leone, N. Bresolin, A. Cross, G. Comi, E.A. Scarpini
GRN rs5848 polymorphism: a role in neurodegeneration?
2009 D. Scalabrini, C. Fenoglio, F. Martinelli Boneschi, M. De Riz, F. Esposito, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Piola, A. Pietroboni, N. Bresolin, D. Galimberti, E. Scarpini
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile