Lista de obras -

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2009

Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis ⬇️

artículo científico publicado el 14 de septiembre de 2013

Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies

artículo científico publicado en 2004

Advantages of QBI in TBSS analyses

artículo científico publicado en 2013

Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report ⬇️

artículo científico publicado el 24 de diciembre de 2012

An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member ⬇️

artículo científico publicado el 1 de mayo de 2013

Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

artículo científico publicado en 2012

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

artículo científico publicado en 2015

Cardiovascular diseases may play a negative role in the prognosis of ALS.

artículo científico publicado en 2018

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

artículo científico publicado en 2012

Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database ⬇️

artículo científico publicado el 1 de enero de 2012

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

artículo científico publicado en 2015

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Exome sequencing reveals VCP mutations as a cause of familial ALS

artículo científico publicado en 2010

Exposure to Environmental Toxicants and Pathogenesis of Amyotrophic Lateral Sclerosis: State of the Art and Research Perspectives ⬇️

artículo científico publicado el 24 de julio de 2013

FUS mutations in sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2010

Factors predicting survival in ALS: a multicenter Italian study

artículo científico publicado en 2016

Functional overlap and divergence between ALS and bvFTD.

artículo científico publicado en 2014

Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy

article

HFE p.H63D polymorphism does not influence ALS phenotype and survival

artículo científico publicado en 2015

High angular resolution diffusion imaging abnormalities in the early stages of amyotrophic lateral sclerosis

artículo científico publicado en 2017

Infratentorial progressive multifocal leukoencephalopathy in a patient treated with fludarabine and rituximab

artículo científico publicado en 2008

Microstructural changes across different clinical milestones of disease in amyotrophic lateral sclerosis

artículo científico publicado en 2015

Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: A 3T high angular resolution diffusion imaging (HARDI) study

Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis

artículo científico publicado en 2016

Protein misfolding, amyotrophic lateral sclerosis and guanabenz: protocol for a phase II RCT with futility design (ProMISe trial).

artículo científico

Proteostasis and ALS: protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS).

artículo científico publicado en 2019

Resting state fMRI correlates of Theory of Mind impairment in amyotrophic lateral sclerosis

artículo científico publicado en 2017

Sporadic ALS is not associated with VAPB gene mutations in Southern Italy

artículo científico publicado en 2006

Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis

artículo científico publicado en 2016

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

artículo científico publicado en 2009

Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging research

artículo científico publicado en 2012

Lista de obras de

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

Accumulation of altered aspartyl residues in erythrocyte membrane proteins from patients with sporadic amyotrophic lateral sclerosis ⬇️

Accuracy of death certificates for amyotrophic lateral sclerosis varies significantly from north to south of Italy: implications for mortality studies

Advantages of QBI in TBSS analyses

Amyotrophic Lateral Sclerosis and Multiple Sclerosis Overlap: A Case Report ⬇️

An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member ⬇️

Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level magnetoencephalographic study

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

Cardiovascular diseases may play a negative role in the prognosis of ALS.

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database ⬇️

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Exome sequencing reveals VCP mutations as a cause of familial ALS

Exposure to Environmental Toxicants and Pathogenesis of Amyotrophic Lateral Sclerosis: State of the Art and Research Perspectives ⬇️

FUS mutations in sporadic amyotrophic lateral sclerosis

Factors predicting survival in ALS: a multicenter Italian study

Functional overlap and divergence between ALS and bvFTD.

Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy

HFE p.H63D polymorphism does not influence ALS phenotype and survival

High angular resolution diffusion imaging abnormalities in the early stages of amyotrophic lateral sclerosis

Infratentorial progressive multifocal leukoencephalopathy in a patient treated with fludarabine and rituximab

Microstructural changes across different clinical milestones of disease in amyotrophic lateral sclerosis

Motor and extramotor neurodegeneration in amyotrophic lateral sclerosis: A 3T high angular resolution diffusion imaging (HARDI) study

Neuropsychological assessment in different King's clinical stages of amyotrophic lateral sclerosis

Protein misfolding, amyotrophic lateral sclerosis and guanabenz: protocol for a phase II RCT with futility design (ProMISe trial).

Proteostasis and ALS: protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS).

Resting state fMRI correlates of Theory of Mind impairment in amyotrophic lateral sclerosis

Sporadic ALS is not associated with VAPB gene mutations in Southern Italy

Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

Widespread structural and functional connectivity changes in amyotrophic lateral sclerosis: insights from advanced neuroimaging research