CORRADO, LUCIA

CORRADO, LUCIA  

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

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Risultati 1 - 11 di 11 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease 2018 Corrado, LuciaTUNESI, SARAFonzo, Alessio DiTrezzi, IlariaComi, Giacomo P. + 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. ComiN. TicozziA. RattiV. Silani + Article (author) -
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 2013 D. CaliniL. CorradoR. Del BoF. VerdeS. CortiC. BertolinG.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. CorradoA. 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. CortiN. TicozziG. ComiV. Silani + Article (author) -
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 2010 L. CorradoR. Del BoA. RattiS. 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) -
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 2000 P. RivaL. CorradoL. Larizza + 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) -
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) -