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 - 11 di 11 (tempo di esecuzione: 0.004 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) -