Lista de obras -

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia

artículo científico publicado en 2002

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

artículo científico publicado en 2015

A new social-family model for eating disorders: A European multicentre project using a case-control design

artículo científico publicado en 2015

A pilot study evaluating the contribution of SLC19A1 (RFC-1) 80G>a polymorphism to Alzheimer's disease in Italian Caucasians

artículo científico publicado en 2014

Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications

artículo científico

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline

artículo científico publicado en 2017

Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up stu

artículo científico publicado en 2016

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.

artículo científico publicado en 2006

Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease

artículo científico publicado en 2011

Association analysis of the paraoxonase-1 gene with Alzheimer's disease.

artículo científico publicado en 2006

Association between serotonin transporter gene polymorphism and eating disorders outcome: a 6-year follow-up study

artículo científico publicado en 2012

Association of IL10 promoter polymorphism in Italian Alzheimer's disease.

artículo científico publicado en 2007

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline

artículo científico publicado en 2017

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

artículo científico

Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians.

artículo científico publicado en 2012

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

artículo científico publicado en 2013

Brain-derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy.

artículo científico publicado en 2004

Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease.

artículo científico publicado en 2004

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020

Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease

artículo científico publicado en 2002

Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians

article

Cystatin C and apoe polymorphisms in Italian Alzheimer's disease.

artículo científico publicado en 2005

DAPK1 is associated with FTD and not with Alzheimer's disease.

artículo científico publicado en 2012

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease

artículo científico publicado en 2010

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

artículo científico publicado en 2017

Effects of donepezil, galantamine and rivastigmine in 938 Italian patients with Alzheimer's disease: a prospective, observational study

artículo científico publicado en 2010

Epigenetic modifications in Alzheimer's disease: cause or effect?

artículo científico publicado en 2015

Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients

artículo científico publicado en 2010

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

artículo científico publicado en 2017

Fragile X premutation with atypical symptoms at onset

artículo científico publicado en 2006

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships

artículo científico publicado en 2017

Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity

article

Heterozygous TREM2 mutations in frontotemporal dementia

artículo científico

Identification of new presenilin gene mutations in early-onset familial Alzheimer disease.

artículo científico publicado en 2003

Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects

artículo científico publicado en 2013

Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease

artículo científico publicado en 2009

Implication of a Genetic Variant at PICALM in Alzheimer's Disease Patients and Centenarians

artículo científico publicado en 2011

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

artículo científico publicado en 2011

Implication of sex and SORL1 variants in italian patients with Alzheimer disease

artículo científico publicado en 2009

Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts

artículo científico publicado en 2006

Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.

artículo científico publicado en 2005

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints

article

Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort

artículo científico publicado en 2008

Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease

artículo científico publicado en 2005

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease

artículo científico publicado en 2010

Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane

artículo científico publicado en 2010

Lipid rafts mediate amyloid-induced calcium dyshomeostasis and oxidative stress in Alzheimer's disease

artículo científico publicado en 2013

Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier

artículo científico publicado en 2017

Membrane cholesterol enrichment prevents Aβ-induced oxidative stress in Alzheimer's fibroblasts.

artículo científico publicado en 2009

Mitochondria and Alzheimer's disease

artículo científico publicado en 2012

Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons

artículo científico publicado en 2015

No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy.

artículo científico publicado en 2007

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

article

Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease.

artículo científico publicado en 2015

Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients

artículo científico publicado en 2002

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype.

artículo científico publicado en 2007

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

artículo científico publicado en 2018

Presenilin mutations linked to familial Alzheimer's disease reduce endoplasmic reticulum and Golgi apparatus calcium levels.

artículo científico publicado en 2006

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

article

Protective effect of new S-acylglutathione derivatives against amyloid-induced oxidative stress

artículo científico publicado en 2008

Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa

artículo científico publicado en 2004

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

artículo científico publicado en 2014

Semantic dementia associated with mutation V363I in the tau gene

artículo científico publicado en 2010

Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference

artículo científico publicado en 2011

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

artículo científico publicado en 2012

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

scientific article published on 23 December 2016

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.

artículo científico publicado en 2013

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations.

artículo científico publicado en 2007

The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts.

artículo científico publicado en 2012

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease.

artículo científico publicado en 2004

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease

article

Lista de obras de

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

A new social-family model for eating disorders: A European multicentre project using a case-control design

A pilot study evaluating the contribution of SLC19A1 (RFC-1) 80G>a polymorphism to Alzheimer's disease in Italian Caucasians

Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline

Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up stu

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.

Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease

Association analysis of the paraoxonase-1 gene with Alzheimer's disease.

Association between serotonin transporter gene polymorphism and eating disorders outcome: a 6-year follow-up study

Association of IL10 promoter polymorphism in Italian Alzheimer's disease.

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians.

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

Brain-derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy.

Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease.

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease

Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians

Cystatin C and apoe polymorphisms in Italian Alzheimer's disease.

DAPK1 is associated with FTD and not with Alzheimer's disease.

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

Effects of donepezil, galantamine and rivastigmine in 938 Italian patients with Alzheimer's disease: a prospective, observational study

Epigenetic modifications in Alzheimer's disease: cause or effect?

Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

Fragile X premutation with atypical symptoms at onset

Frontotemporal dementia and its subtypes: a genome-wide association study

Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships

Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity

Heterozygous TREM2 mutations in frontotemporal dementia

Identification of new presenilin gene mutations in early-onset familial Alzheimer disease.

Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects

Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease

Implication of a Genetic Variant at PICALM in Alzheimer's Disease Patients and Centenarians

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

Implication of sex and SORL1 variants in italian patients with Alzheimer disease

Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts

Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints

Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort

Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease

Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane

Lipid rafts mediate amyloid-induced calcium dyshomeostasis and oxidative stress in Alzheimer's disease

Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier

Membrane cholesterol enrichment prevents Aβ-induced oxidative stress in Alzheimer's fibroblasts.

Mitochondria and Alzheimer's disease

Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons

No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy.

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease.

Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Presenilin mutations linked to familial Alzheimer's disease reduce endoplasmic reticulum and Golgi apparatus calcium levels.

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

Protective effect of new S-acylglutathione derivatives against amyloid-induced oxidative stress

Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Semantic dementia associated with mutation V363I in the tau gene

Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations.

The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts.

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease.

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease