CORRADO, LUCIA

CORRADO, LUCIA  

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

Mostra records
Risultati 1 - 16 di 16 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis 2021 Ahmed S.Ticozzi N.Fallini C.Tiloca C.Colombrita C.Calini D.Pensato V.Castellotti B.Comi G. P.Del Bo R.Gagliardi S.Lauria G.Duga S.Corti S.Cereda C.Corrado L.Taroni F.Ratti A.Fratta P.Landi F.Lleo A.Galimberti D.Scarpini E.Serpente M.Zecca C.Ghidoni R.Silani V. + Article (author) -
Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy 2020 Nicola TicozziPietro FrattaCristina CeredaRoberto Del BoStefania CortiGiacomo P. ComiLucia CorradoCinzia BertolinViviana PensatoCinzia TilocaAntonia RattiChiara ZeccaDaniela CaliniVincenzo SilaniBarbara CastellottiEnrica Bersano + Article (author) -
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease 2018 Corrado, LuciaTUNESI, SARAFonzo, Alessio DiTrezzi, IlariaCereda, CristinaComi, Giacomo P. + Article (author) -
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis 2016 Ticozzi N.Tiloca C.Colombrita C.Verde F.Lauria G.Ratti A.Silani V.Comi G. P.Del Bo R.Corti S.Cereda C.Corrado L.Pensato V.Castellotti B. + Article (author) -
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 2015 C. TilocaL. CorradoC. BertolinR. DEL BOD. CaliniG. LAURIA PINTERS.P. CortiG.M.E.A. Solda'S. DugaG.P. ComiC. CeredaN. TicozziA. RattiV. Silani + Article (author) -
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 2015 Vincenzo SilaniNicola TicozziStefano DugaLucia CorradoDaniela CaliniClaudia ColombritaAntonia RattiCinzia TilocaCinzia BertolinBarbara CastellottiViviana PensatoCristina CeredaGiuseppe LauriaStefania CortiRoberto Del Bo + Article (author) -
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 2013 D. CaliniL. CorradoR. Del BoF. VerdeS. CortiC. BertolinC. CeredaG.P. ComiN. TicozziA. RattiV. Silani + Article (author) -
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia 2012 C. TilocaR. Del BoL. CorradoC. CeredaA. RattiS. CortiP. MilaniG. RiboldiF. TaroniG.P. ComiN. TicozziV. Silani + Conference Object -
Optineurin gene mutations in a Cohort of Italian Amyotrophic Lateral Sclerosis patients 2011 R. Del BoC. TilocaL. CorradoA. RattiS. CortiC. CeredaN. TicozziG. ComiV. Silani + Article (author) -
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 2011 Corrado L.Cereda C. + Article (author) -
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 2010 L. CorradoR. Del BoA. RattiC. CeredaS. PencoC. ColombritaGAGLIARDI, STEFANOG.P. ComiV. Silani + Article (author) -
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 Corrado L.Pileggi S. + Article (author) -
Erratum: Fish with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies (Chromosome reseach (2001) 9 (167-170)) 2001 Bentivegna A.Venturin M.Gervasini C.Corrado L.Larizza L.Riva P. Article (author) -
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype 2000 L. CorradoP. RivaM. MiozzoL. Larizza + Article (author) -
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 2000 P. RivaL. CorradoL. Larizza + Article (author) -
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 1999 L. CorradoP. ColapietroL. LarizzaP. Riva Article (author) -