TICOZZI, NICOLA

TICOZZI, NICOLA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Risultati 1 - 20 di 116 (tempo di esecuzione: 0.136 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Advance care planning and mental capacity in ALS: a current challenge for an unsolved matter 20-mag-2020 Ticozzi N.Silani V. + Article (author) -
ALS genes: a mutational screening in a large cohort of Italian patients 1-gen-2008 N. TicozziA. RattiV. Silani + Article (author) -
ALS Genes: mutational analysis in a large cohort of Italian patients 1-gen-2009 N. TicozziA. RattiC. ColombritaV. Silani + Book Part (author) -
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function 1-nov-2018 N. TicozziC. TilocaF. VerdeS. DugaA. RattiV. Silani + Article (author) -
Amyotrophic lateral sclerosis: Epidemiology and risk factors 1-gen-2016 Verde F.Ticozzi N. Book Part (author) -
Amyotrophic lateral sclerosis: Genotypes and phenotypes 1-gen-2014 Ticozzi N.Silani V. Book Part (author) -
Analysis of FUS Gene Mutation in Familial Amyotrophic Lateral Sclerosis within an Italian cohort 1-gen-2009 N. TicozziV. SilaniA. Ratti + Article (author) -
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) -
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 1-gen-2014 N. TicozziA. RattiR. Del BoS. CortiV. Silani + Article (author) -
Angiogenin gene mutations in Italian patients with familial and sporadic ALS 1-gen-2007 N. TicozziC. ColombritaA. RattiV. Silani + Article (author) -
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis 1-gen-2011 N. TicozziV. Silani + Article (author) -
Angiogenin: a novel candidate gene for ALS pathogenesis in the Italian Population 1-gen-2007 C. ColombritaN. TicozziA. RattiV. Silani + Article (author) -
The Arrows and Colors Cognitive Test (ACCT) : a new verbal-motor free cognitive measure for executive functions in ALS 1-gen-2018 B. PolettiF. SolcaN. TicozziV. Silani + Article (author) -
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis 1-lug-2016 C. TilocaA. RattiR. Del BoG.P. ComiN. TicozziV. Silani + Article (author) -
Association of clinically evident eye movement abnormalities with motor and cognitive features in patients with motor neuron disorders 2-nov-2021 Solca, FedericaDiena, AlbertoColombo, EleonoraMaranzano, AlessioFerrucci, RobertaVerde, FedericoSilani, VincenzoTicozzi, Nicola + Article (author) -
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 30-ago-2021 Ticozzi N.Silani V.Ticozzi N.Colombrita C.Comi G. P.Del Bo R.Lauria G.Corti S.Ratti A.Silani V. + Article (author) -
ATAXIN2 CAG-repeat length in Italians patients with amyotrophic lateral sclerosis : risk factor or variant phenotype? Implication for genetic testing and counseling 1-gen-2012 N. TicozziG. LauriaV. Silani + Article (author) -
Brain-Computer Interface for Clinical Purposes : Cognitive Assessment and Rehabilitation 1-gen-2017 Solca, FedericaSangalli, DavideTicozzi, NicolaSilani, VincenzoPoletti, Barbara + Article (author) -
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder 1-gen-2013 V. SilaniN. Ticozzi + Article (author) -
C9ORF72 repeat expansion in a large Italian ALS cohort : evidence of a founder effect 1-ott-2012 A. RattiR. Del BoC. TilocaM. RanieriS.P. CortiN. TicozziG.P. ComiV. Silani + Article (author) -