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Mostrati risultati da 1 a 11 di 11
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 1-giu-1999 L. CorradoP. ColapietroL. LarizzaP. Riva Article (author) -
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 1-gen-2000 P. RivaL. CorradoL. Larizza + Article (author) -
Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype 18-dic-2000 L. CorradoP. RivaM. MiozzoL. Larizza + Article (author) -
Erratum: Fish with locus-specific probes on stretched chromosomes: A useful tool for genome organization studies (Chromosome reseach (2001) 9 (167-170)) 1-ago-2001 Bentivegna A.Venturin M.Gervasini C.Corrado L.Larizza L.Riva P. 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 1-gen-2007 Corrado L.Pileggi S. + Article (author) -
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 1-mar-2010 L. CorradoR. Del BoA. RattiS. PencoC. ColombritaGAGLIARDI, STEFANOG.P. ComiV. Silani + Article (author) -
Optineurin gene mutations in a Cohort of Italian Amyotrophic Lateral Sclerosis patients 1-gen-2011 R. Del BoC. TilocaL. CorradoA. RattiS. CortiN. TicozziG. ComiV. Silani + Article (author) -
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia 1-gen-2012 C. TilocaR. Del BoL. CorradoA. RattiS. CortiP. MilaniG. RiboldiF. TaroniG.P. ComiN. TicozziV. Silani + Conference Object -
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 1-nov-2013 D. CaliniL. CorradoR. Del BoF. VerdeS. CortiC. BertolinG.P. ComiN. TicozziA. RattiV. Silani + Article (author) -
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 1-mag-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) -
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease 29-mar-2018 Corrado, LuciaTUNESI, SARAFonzo, Alessio DiTrezzi, IlariaComi, Giacomo P. + Article (author) -
Mostrati risultati da 1 a 11 di 11
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