Sfoglia per Autore
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR
1999 L. Corrado, P. Colapietro, L. Larizza, P. Riva
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes
2000 P. Riva, L. Corrado, F. Natacci, P. Castorina, B. L. Wu, G. H. Schneider, M. Clementi, R. Tenconi, B. R. Korf, L. Larizza
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype
2000 F. Natacci, L. Corrado, M. Pierri, M. Rossetti, C. Zuccarini, P. Riva, M. Miozzo, L. Larizza
Erratum: Fish with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies (Chromosome reseach (2001) 9 (167-170))
2001 A. Bentivegna, M. Venturin, C. Gervasini, L. Corrado, L. Larizza, P. Riva
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population
2007 L. Corrado, S. Battistini, S. Penco, L. Bergamaschi, L. Testa, C. Ricci, F. Giannini, G. Greco, M.C. Patrosso, S. Pileggi, R. Causarano, L. Mazzini, P. Momigliano-Richiardi, S. D'Alfonso
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
2010 L. Corrado, R. Del Bo, B. Castellotti, A. Ratti, C. Cereda, S. Penco, G. Sorarù, Y. Carlomagno, S. Ghezzi, V. Pensato, C. Colombrita, S. Gagliardi, L. Cozzi, V. Orsetti, M. Mancuso, G. Siciliano, L. Mazzini, G.P. Comi, C. Gellera, M. Ceroni, S. D'Alfonso, V. Silani
Optineurin gene mutations in a Cohort of Italian Amyotrophic Lateral Sclerosis patients
2011 R. Del Bo, C. Tiloca, V. Pensato, L. Corrado, A. Ratti, S. Corti, B. Castellotti, B. Luciano, G. Soraru, C. Cereda, L. Mazzini, N. Ticozzi, C. Gellera, G. Comi, V. Silani
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia
2012 C. Gellera, C. Tiloca, R. Del Bo, L. Corrado, V. Pensato, J. Agostini, C. Cereda, A. Ratti, B. Castellotti, S. Corti, A. Bagarotti, A. Cagnin, P. Milani, C. Gabelli, G. Riboldi, L. Mazzini, G. Sorarù, S. D'Alfonso, F. Taroni, G.P. Comi, N. Ticozzi, V. Silani
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis
2013 D. Calini, L. Corrado, R. Del Bo, S. Gagliardi, V. Pensato, F. Verde, S. Corti, L. Mazzini, P. Milani, B. Castellotti, C. Bertolin, G. Sorarù, C. Cereda, G.P. Comi, S. D'Alfonso, C. Gellera, N. Ticozzi, J.E. Landers, A. Ratti, V. Silani
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations
2015 V. Pensato, C. Tiloca, L. Corrado, C. Bertolin, V. Sardone, R. DEL BO, D. Calini, J. Mandrioli, G. LAURIA PINTER, L. Mazzini, G. Querin, M. Ceroni, R. Cantello, S.P. Corti, B. Castellotti, G.M.E.A. Solda', S. Duga, G.P. Comi, C. Cereda, G. Sorarù, S. D'Alfonso, F. Taroni, C.E. Shaw, J.E. Landers, N. Ticozzi, A. Ratti, C. Gellera, V. Silani
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease
2018 L. Corrado, F. De Marchi, S. Tunesi, G.D. Oggioni, M. Carecchio, L. Magistrelli, S. Tesei, G. Riboldazzi, A.D. Fonzo, C. Locci, I. Trezzi, R. Zangaglia, C. Cereda, S. D'Alfonso, C. Magnani, G.P. Comi, G. Bono, C. Pacchetti, R. Cantello, S. Goldwurm, C. Comi
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