about
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisMutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisNEK1 variants confer susceptibility to amyotrophic lateral sclerosisReduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisA genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyMutational analysis of TARDBP in neurodegenerative diseasesParaoxonase gene mutations in amyotrophic lateral sclerosis.The diagnosis of Amyotrophic lateral sclerosis in 2010.Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations.Novel mutations support a role for Profilin 1 in the pathogenesis of ALS.Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementiaCCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortStem cells in amyotrophic lateral sclerosis: motor neuron protection or replacement?Genetics of familial Amyotrophic lateral sclerosis.RNA-binding proteins and RNA metabolism: a new scenario in the pathogenesis of Amyotrophic lateral sclerosis.Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.A review of options for treating sialorrhea in amyotrophic lateral sclerosis.The role of de novo mutations in the development of amyotrophic lateral sclerosis.An eye-tracker controlled cognitive battery: overcoming verbal-motor limitations in ALS.Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS).A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotypeGenome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.Brain-Computer Interface for Clinical Purposes: Cognitive Assessment and RehabilitationC9orf72 repeat expansions are restricted to the ALS-FTD spectrum.C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect.Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis.ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients.Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia.An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases.Cognitive assessment in Amyotrophic Lateral Sclerosis by means of P300-Brain Computer Interface: a preliminary study.Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt-Jakob disease.
P50
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Nicola Ticozzi
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Nicola Ticozzi
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Nicola Ticozzi
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Nicola Ticozzi
@nl
Nicola Ticozzi
@sl
type
label
Nicola Ticozzi
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Nicola Ticozzi
@en
Nicola Ticozzi
@es
Nicola Ticozzi
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Nicola Ticozzi
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prefLabel
Nicola Ticozzi
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Nicola Ticozzi
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Nicola Ticozzi
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Nicola Ticozzi
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Nicola Ticozzi
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P1053
K-8094-2016
P106
P1153
23062054500
P21
P31
P3829
P496
0000-0001-5963-7426