CORRADO, LUCIA
CORRADO, LUCIA
DIPARTIMENTO DI BIOLOGIA E GENETICA PER LE SCIENZE MEDICHE (attivo dal 01/11/1983 al 26/04/2012)
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
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
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
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
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
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
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
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
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
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
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