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Lista de obras de Giuliano Binetti

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

artículo científico publicado en 2016

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 novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

artículo científico publicado en 2011

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

artículo científico publicado en 2006

A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expression.

artículo científico publicado en 2011

A transcultural study of agitation in dementia.

artículo científico publicado en 2002

A window into the heterogeneity of human cerebrospinal fluid Aβ peptides

artículo científico publicado en 2011

Abnormal fronto-parietal coupling of brain rhythms in mild Alzheimer's disease: a multicentric EEG study.

artículo científico publicado en 2004

Action and object naming in frontotemporal dementia, progressive supranuclear palsy, and corticobasal degeneration.

artículo científico

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

scientific article published on 03 December 2019

Altered Expression of Circulating Cdc42 in Frontotemporal Lobar Degeneration.

artículo científico publicado en 2018

Alzheimer disease-associated cystatin C variant undergoes impaired secretion

artículo científico publicado en 2003

An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease

artículo científico publicado en 2011

An electronic memory aid to support prospective memory in patients in the early stages of Alzheimer's disease: a pilot study.

artículo científico publicado en 2003

Analysis of alpha-2-macroglobulin-2 allele as a risk factor in Alzheimer's disease.

artículo científico publicado en 2001

Analysis of grey matter in thalamus and basal ganglia based on EEG α3/α2 frequency ratio reveals specific changes in subjects with mild cognitive impairment

artículo científico publicado en 2012

Anatomical Substrate and Scalp EEG Markers are Correlated in Subjects with Cognitive Impairment and Alzheimer's Disease

artículo científico publicado en 2011

Apolipoprotein E and alpha brain rhythms in mild cognitive impairment: a multicentric electroencephalogram study.

artículo científico publicado en 2006

Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's disease.

artículo científico publicado en 2004

Areas of intervention for genetic counselling of dementia: cross-cultural comparison between Italians and Americans

artículo científico publicado en 2006

Association between small apolipoprotein(a) isoforms and frontotemporal dementia in humans.

artículo científico publicado en 2003

Association of blood pressure and genetic background with white matter lesions in patients with mild cognitive impairment.

artículo científico publicado en 2008

Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2.

artículo científico publicado en 2003

Atypical dementia associated with a novel presenilin-2 mutation

artículo científico publicado en 2003

BACE-2 is overexpressed in Down's syndrome.

artículo científico publicado en 2003

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

scientific article published on 01 January 2011

Behavioral and neurophysiological effects of transdermal rotigotine in atypical parkinsonism.

artículo científico publicado en 2014

Blockade of the tumor necrosis factor-related apoptosis inducing ligand death receptor DR5 prevents beta-amyloid neurotoxicity.

artículo científico publicado en 2006

C9ORF72 Hexanucleotide Repeat Number in Frontotemporal Lobar Degeneration: A Genotype-Phenotype Correlation Study

artículo científico publicado en 2015

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study

artículo científico publicado en 2014

C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

artículo científico publicado en 2013

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

scientific article published on 17 September 2020

CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2009

Cerebrospinal fluid biomarkers for Alzheimer's disease: the present and the future.

scientific article published on 25 June 2011

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

artículo científico publicado en 2011

Characterization and distribution of protein kinase C isoforms in human skin fibroblasts

scientific article published on 01 October 1994

Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer's disease

artículo científico publicado en 2009

Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementia.

artículo científico publicado en 2005

Clinical and neuropsychological features associated with structural imaging patterns in patients with mild cognitive impairment

artículo científico publicado en 2007

Cognitive telerehabilitation in mild cognitive impairment, Alzheimer's disease and frontotemporal dementia: A systematic review

artículo científico publicado en 2017

Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

artículo científico publicado en 2017

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

Comparison of the effects of transdermal and oral rivastigmine on cognitive function and EEG markers in patients with Alzheimer's disease

artículo científico publicado en 2014

Computed tomography in the detection of the vascular component in dementia.

artículo científico publicado en 1995

Copper dyshomeostasis in Wilson disease and Alzheimer's disease as shown by serum and urine copper indicators.

artículo científico publicado en 2017

Cystatin C is released in association with exosomes: a new tool of neuronal communication which is unbalanced in Alzheimer's disease.

artículo científico publicado en 2009

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

artículo científico publicado en 2009

Decreased plasma levels of soluble receptor for advanced glycation end products in mild cognitive impairment.

artículo científico publicado en 2008

Defective protein kinase C alpha leads to impaired secretion of soluble beta-amyloid precursor protein from Alzheimer's disease fibroblasts.

artículo científico publicado en 1996

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

artículo científico publicado en 2017

Delusions and dementia: clinical and CT correlates.

artículo científico publicado en 1995

Dementia, delusions and seizures: storage disease or genetic AD?

artículo científico publicado en 2007

Detection of the presenilin 1 COOH-terminal fragment in the extracellular compartment: a release enhanced by apoptosis

scientific journal article

Diagnostic and prognostic value of serum NfL and p-Tau181 in frontotemporal lobar degeneration

artículo científico publicado en 2020

Distinct cerebrospinal fluid amyloid-beta peptide signatures in cognitive decline associated with Alzheimer's disease and schizophrenia.

artículo científico publicado en 2012

EEG markers are associated to gray matter changes in thalamus and basal ganglia in subjects with mild cognitive impairment.

artículo científico publicado en 2011

EEG markers discriminate among different subgroup of patients with mild cognitive impairment.

artículo científico publicado en 2009

EEG upper/low alpha frequency power ratio and the impulsive disorders network in subjects with mild cognitive impairment.

artículo científico publicado en 2014

EEG upper/low alpha frequency power ratio relates to temporo-parietal brain atrophy and memory performances in mild cognitive impairment.

artículo científico publicado en 2013

Effect of age and education on performance on the Mini-Mental State Examination in a healthy older population and during the course of Alzheimer's disease.

artículo científico publicado en 1995

Effect of energy shortage and oxidative stress on amyloid precursor protein metabolism in COS cells.

artículo científico publicado en 1997

Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter

artículo científico publicado en 2008

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

Effects of estrogens on cognition and brain morphology: involvement of the cerebellum.

artículo científico publicado en 2005

Effects of hormone therapy on brain morphology of healthy postmenopausal women: a Voxel-based morphometry study.

artículo científico publicado en 2006

Electroencephalographic upper/low alpha frequency power ratio relates to cortex thinning in mild cognitive impairment.

artículo científico publicado en 2014

Estimating the age of the most common Italian GRN mutation: walking back to Canossa times

artículo científico publicado en 2013

Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease

artículo científico publicado en 2010

Exosomes: the Trojan horses of neurodegeneration.

artículo científico publicado en 2008

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

scientific article published on 01 January 2010

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

Free copper and resting temporal EEG rhythms correlate across healthy, mild cognitive impairment, and Alzheimer's disease subjects.

artículo científico publicado en 2007

Free copper distinguishes mild cognitive impairment subjects from healthy elderly individuals.

artículo científico publicado en 2011

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

artículo científico publicado en 2014

GRN variability contributes to sporadic frontotemporal lobar degeneration

artículo científico publicado en 2010

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.

artículo científico publicado en 2016

Genetic association of an alpha2-macroglobulin (Val1000lle) polymorphism and Alzheimer's disease.

artículo científico publicado en 1998

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

artículo científico publicado en 2015

Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2012

Genotype (cystatin C) and EEG phenotype in Alzheimer disease and mild cognitive impairment: a multicentric study

artículo científico publicado en 2005

Genotypes and haplotypes in the IL-1 gene cluster: analysis of two genetically and diagnostically distinct groups of Alzheimer patients.

artículo científico publicado en 2005

H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers.

artículo científico publicado en 2008

HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans.

artículo científico publicado en 2009

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

artículo científico publicado en 2000

Hippocampal atrophy and EEG markers in subjects with mild cognitive impairment

artículo científico publicado en 2007

Homocysteine and electroencephalographic rhythms in Alzheimer disease: a multicentric study.

artículo científico publicado en 2007

Increase of theta frequency is associated with reduction in regional cerebral blood flow only in subjects with mild cognitive impairment with higher upper alpha/low alpha EEG frequency power ratio.

artículo científico publicado en 2013

Increase of theta/gamma and alpha3/alpha2 ratio is associated with amygdalo-hippocampal complex atrophy.

artículo científico publicado en 2009

Increase of theta/gamma ratio is associated with memory impairment.

artículo científico publicado en 2009

Increasing hippocampal atrophy and cerebrovascular damage is differently associated with functional cortical coupling in MCI patients.

artículo científico publicado en 2009

Inhibition of energy metabolism down-regulates the Alzheimer related presenilin 2 gene.

artículo científico publicado en 2003

Interaction between tau and alpha-synuclein proteins is impaired in the presence of P301L tau mutation.

artículo científico publicado en 2005

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

artículo científico publicado en 2010

Is cognitive function linked to serum free copper levels? A cohort study in a normal population.

artículo científico publicado en 2010

Late onset neurodegenerative diseases: a theoretical point of view.

artículo científico publicado en 2008

Longitudinal prognostic value of serum "free" copper in patients with Alzheimer disease.

artículo científico publicado en 2009

Losing protein in the brain: the case of progranulin.

artículo científico

Loss of Neuroprotective Factors in Neurodegenerative Dementias: The End or the Starting Point?

artículo científico publicado en 2017

Loss of exosomes in progranulin-associated frontotemporal dementia

artículo científico publicado en 2016

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

artículo científico publicado en 2008

Mapping distributed sources of cortical rhythms in mild Alzheimer's disease. A multicentric EEG study

artículo científico publicado en 2004

Mapping the effect of APOE epsilon4 on gray matter loss in Alzheimer's disease in vivo

artículo científico publicado en 2009

Markers of Alzheimer's disease in a population attending a memory clinic.

artículo científico publicado en 2009

Medial temporal atrophy but not memory deficit predicts progression to dementia in patients with mild cognitive impairment.

artículo científico publicado en 2006

Mini-Mental State Examination: a normative study in Italian elderly population

artículo científico publicado en 1996

No association between DCP1 genotype and late-onset Alzheimer disease.

artículo científico publicado en 2002

Non-ergot dopamine agonist rotigotine as a promising therapeutic tool in atypical parkinsonism syndromes: a 24 months pilot observational open-label study.

artículo científico publicado en 2014

Novel T719P AbetaPP mutation unbalances the relative proportion of amyloid-beta peptides.

artículo científico publicado en 2009

Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study

artículo científico publicado en 2011

Optimization protocol for amyloid-β peptides detection in human cerebrospinal fluid using SELDI TOF MS.

artículo científico publicado en 2010

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

artículo científico publicado en 2016

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

artículo científico publicado en 2020

Pattern of structural and functional brain abnormalities in asymptomatic granulin mutation carriers.

artículo científico publicado en 2014

Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.

artículo científico publicado en 2013

Plasma cystatin C and risk of developing Alzheimer's disease in subjects with mild cognitive impairment.

artículo científico publicado en 2010

Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease

artículo científico publicado en 2004

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

Predictors of Mortality and Institutionalization in Alzheimer Disease Patients 1 Year after Discharge from an Alzheimer Dementia Unit

scholarly article by Angelo Bianchetti et al published 1995 in Dementia and Geriatric Cognitive Disorders

Predictors of cognitive improvement after reality orientation in Alzheimer's disease.

artículo científico publicado en 2002

Predictors of comprehensive stimulation program efficacy in patients with cognitive impairment. Clinical practice recommendations.

artículo científico publicado en 2012

Preliminary evidence of validity of the revised criteria for Alzheimer disease diagnosis: report of 2 cases.

artículo científico publicado en 2010

Presenilin 2 is secreted in mouse primary neurons: a release enhanced by apoptosis.

artículo científico publicado en 2007

Presenilin 2 mutations alter cystatin C trafficking in mouse primary neurons.

artículo científico publicado en 2006

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

artículo científico publicado en 2006

Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

artículo científico publicado en 2015

Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients

article

Prevalence of pathogenic mutations in an Italian clinical series of patients with familial dementia.

artículo científico publicado en 2004

Procedural memory stimulation in Alzheimer's disease: impact of a training programme.

artículo científico publicado en 1997

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

artículo científico publicado en 2008

Progranulin Mutations Affects Brain Oscillatory Activity in Fronto-Temporal Dementia.

artículo científico publicado en 2016

Progranulin Mutations are a Common Cause of FTLD in Northern Italy ⬇️

artículo científico publicado el 1 de julio de 2010

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

artículo científico publicado en 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

artículo científico publicado en 2014

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

artículo científico publicado en 2018

Reduction of Ca2+ stores and capacitative Ca2+ entry is associated with the familial Alzheimer's disease presenilin-2 T122R mutation and anticipates the onset of dementia.

artículo científico publicado en 2005

Regional atrophy of transcallosal prefrontal connections in cognitively normal APOE epsilon4 carriers.

artículo científico publicado en 2009

Relation of apolipoprotein(a) size to alzheimer's disease and vascular dementia.

artículo científico publicado en 2004

Replication study to confirm the role of CYP2D6 polymorphism rs1080985 on donepezil efficacy in Alzheimer's disease patients.

artículo científico publicado en 2012

Risk of mortality and institutionalization in demented patients with delusions.

artículo científico publicado en 1996

Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.

artículo científico publicado en 2011

Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.

artículo científico publicado en 2011

Rotigotine is safe and efficacious in Atypical Parkinsonism Syndromes induced by both α-synucleinopathy and tauopathy.

artículo científico publicado en 2014

Secretory leukocyte protease inhibitor protein regulates the penetrance of frontotemporal lobar degeneration in progranulin mutation carriers.

artículo científico publicado en 2014

Semantic memory in Alzheimer's disease: an analysis of category fluency.

artículo científico

Serum C-Peptide, Visfatin, Resistin, and Ghrelin are Altered in Sporadic and GRN-Associated Frontotemporal Lobar Degeneration

artículo científico publicado en 2017

Sources of cortical rhythms change as a function of cognitive impairment in pathological aging: a multicenter study.

artículo científico publicado en 2005

Sources of cortical rhythms in adults during physiological aging: A multicentric EEG study

artículo científico publicado en 2006

Specific EEG changes associated with atrophy of hippocampus in subjects with mild cognitive impairment and Alzheimer's disease.

artículo científico publicado en 2012

Strengthening of Existing Episodic Memories Through Non-invasive Stimulation of Prefrontal Cortex in Older Adults with Subjective Memory Complaints.

artículo científico publicado en 2017

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

scientific article published on 23 December 2016

TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

scientific article published on July 2013

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.

artículo científico publicado en 2010

Tau Rather than TDP-43 Proteins are Potential Cerebrospinal Fluid Biomarkers for Frontotemporal Lobar Degeneration Subtypes: A Pilot Study.

artículo científico publicado en 2016

Tau missing from CSF: a case report.

artículo científico publicado en 2007

Temporal lobe asymmetry in patients with Alzheimer's disease with delusions

artículo científico publicado en 2000

The CST3 B haplotype is associated with frontotemporal lobar degeneration.

artículo científico publicado en 2009

The H1 haplotype of the tau gene (MAPT) is associated with mild cognitive impairment.

artículo científico publicado en 2010

The H2 MAPT haplotype is associated with familial frontotemporal dementia.

artículo científico publicado en 2006

The Heritability of Frontotemporal Lobar Degeneration: Validation of Pedigree Classification Criteria in a Northern Italy Cohort.

artículo científico publicado en 2017

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

artículo científico publicado en 2012

The level of 24-Hydroxycholesteryl Esters is an Early Marker of Alzheimer's Disease.

artículo científico publicado en 2016

Value of serum nonceruloplasmin copper for prediction of mild cognitive impairment conversion to Alzheimer disease.

artículo científico publicado en 2014

Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239I

artículo científico publicado en 2000

Vascular damage and EEG markers in subjects with mild cognitive impairment.

artículo científico publicado en 2007

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