CALINI, DANIELA

CALINI, DANIELA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
TARDBP mutations in a cohort of Italian patients with Parkinson’s disease and atypical parkinsonisms 2022 Tiloca, CinziaCalcagno, NarghesVerde, FedericoPeverelli, SilviaCalini, DanielaSangalli, DavideRatti, AntoniaSilani, VincenzoTicozzi, Nicola + Article (author) -
The validation of the Italian Edinburgh cognitive and behavioural ALS screen (ECAS) 2016 B. PolettiF. SolcaA. MontiS. ZagoD. CaliniC. TilocaA. DorettiF. VerdeA. RattiN. TicozziV. Silani + 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) -
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories 2014 A. RattiD. CaliniV. Silani + Article (author) -
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 2014 A. RattiC. TilocaS. CortiD. GentiliniD. CaliniR. Del BoN. TicozziG.P. ComiV. Silani + Article (author) -
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum 2014 N. TicozziC. TilocaD. CaliniALTIERI, ALESSANDRAC. ColombritaA. RattiV. Silani + Article (author) -
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 2014 N. TicozziD. CaliniC. TilocaC. ColombritaG.P. ComiR. Del BoG. LauriaS. CortiA. 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) -