CALINI, DANIELA

CALINI, DANIELA  

Universita' degli Studi di MILANO  

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Risultati 1 - 11 di 11 (tempo di esecuzione: 0.0 secondi).
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) -
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 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. 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) -
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) -
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum 2014 N. TicozziC. TilocaD. CaliniALTIERI, ALESSANDRAC. ColombritaC. CeredaA. RattiV. 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. TilocaC. CeredaS. CortiD. GentiliniD. CaliniR. Del BoN. TicozziG.P. ComiV. 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. CortiC. CeredaA. 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. BertolinC. CeredaG.P. ComiN. TicozziA. RattiV. Silani + Article (author) -