Lista de obras -

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

artículo científico publicado en 2002

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 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

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

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

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

artículo científico publicado en 2015

Fragile X premutation with atypical symptoms at onset

artículo científico publicado en 2006

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

article

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

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

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

artículo científico publicado en 2017

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

artículo científico publicado en 2014

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

artículo científico publicado en 2007

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

artículo científico publicado en 2015

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

article

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

Semantic dementia associated with mutation V363I in the tau gene

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

artículo científico publicado en 2013

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

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 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.

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.

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

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

Fragile X premutation with atypical symptoms at onset

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

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

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

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

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

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

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

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

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

Semantic dementia associated with mutation V363I in the tau gene

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

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

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