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Lista de obras de Sandro Sorbi

5-HT2A receptor gene polymorphism and eating disorders

artículo científico publicado en 2002

5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa

article

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

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

artículo científico publicado en 2002

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2013

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

artículo científico publicado en 2015

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

artículo científico publicado en 2013

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

A short version of Rao's Brief Repeatable Battery as a screening tool for cognitive impairment in multiple sclerosis.

artículo científico publicado en 2009

APOE-epsilon4 is not associated with cognitive impairment in relapsing-remitting multiple sclerosis

artículo científico publicado en 2009

APP717 and Alzheimer's disease in Italy.

artículo científico publicado en 1993

Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population

artículo científico publicado en 2003

Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees

article

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

artículo científico

Age and ApoE genotype interaction in Alzheimer's disease: an FDG-PET study

artículo científico publicado en 2004

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

Alteration of acylphosphatase levels in familial Alzheimer's disease fibroblasts with presenilin gene mutations.

artículo científico publicado en 1996

Alzheimer skin fibroblasts show increased susceptibility to free radicals.

artículo científico publicado en 1992

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline

artículo científico publicado en 2017

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

artículo científico publicado en 1996

Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits.

artículo científico publicado en 2005

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

artículo científico publicado en 2011

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

Analysis of apolipoprotein E, α1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man

article

Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease

article

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

artículo científico publicado en 2006

Anosognosia in very mild Alzheimer's disease but not in mild cognitive impairment.

artículo científico publicado en 2005

Anti-ganglioside antibodies and elevated CSF IgG levels in Guillain-Barre syndrome

artículo científico publicado en 2006

ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease.

artículo científico publicado en 1994

ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families.

artículo científico publicado en 1995

Apolipoprotein E and ?1-antichymotrypsin polymorphism in Alzheimer's disease

artículo científico publicado en 1996

Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease

artículo científico publicado en 1995

ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis

artículo científico publicado en 2009

Are there adaptive changes in the human brain of patients with Parkinson's disease treated with long-term deep brain stimulation of the subthalamic nucleus? A 4-year follow-up study with regional cerebral blood flow SPECT.

artículo científico publicado en 2007

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 BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

artículo científico publicado en 2004

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations

artículo científico publicado en 2005

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

artículo científico publicado en 2007

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

artículo científico publicado en 2008

Association of Neocortical Volume Changes With Cognitive Deterioration in Relapsing-Remitting Multiple Sclerosis

artículo científico publicado en 2007

Association of apolipoprotein E polymorphism to clinical heterogeneity of multiple sclerosis

artículo científico publicado en 2000

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

artículo científico publicado en 2017

Association of the estrogen receptor alpha gene polymorphisms with sporadic Alzheimer's disease.

artículo científico publicado en 1999

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

artículo científico

Association studies between the plasmin genes and late-onset Alzheimer's disease

artículo científico publicado en 2007

Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease

artículo científico publicado en 2002

Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors.

artículo científico publicado en 2008

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

artículo científico publicado en 2012

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Autologous hematopoietic stem cell transplantation for very active relapsing-remitting multiple sclerosis: report of two cases

artículo científico publicado en 2007

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

artículo científico publicado en 2013

Benign multiple sclerosis

artículo científico publicado en 2006

Brain damage as detected by magnetization transfer imaging is less pronounced in benign than in early relapsing multiple sclerosis

artículo científico publicado en 2006

Brain metabolic correlates of dopaminergic degeneration in de novo idiopathic Parkinson's disease

artículo científico publicado en 2009

Brain metabolic decreases related to the dose of the ApoE e4 allele in Alzheimer's disease

artículo científico publicado en 2004

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

Case???control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa

article

Cathepsin D expression is decreased in Alzheimer's disease fibroblasts

scholarly article by Lorena Urbanelli et al published January 2008 in Neurobiology of Aging

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

artículo científico publicado en 2002

Changes in high affinity choline uptake in rat cortex following lesions of the magnocellular forebrain nuclei

artículo científico publicado en 1982

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

article

Choline High-Affinity Uptake and Metabolism and Choline Acetyltransferase Activity in the Striatum of Rats Chronically Treated with Neuroleptics ⬇️

artículo científico publicado el 1 de septiembre de 1980

Clinical and genetic analysis of an Italian family with Machado-Joseph disease

article

Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy.

artículo científico publicado en 2001

Clinical and genetic study of a large SPG4 Italian family

artículo científico publicado en 2005

Clinical correlation of the binding potential with 123I-FP-CIT in de novo idiopathic Parkinson's disease patients

artículo científico publicado en 2008

Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis

article

Cognitive and affective changes in mild to moderate Alzheimer's disease patients undergoing switch of cholinesterase inhibitors: a 6-month observational study

artículo científico publicado en 2014

Cognitive assessment and quantitative magnetic resonance metrics can help to identify benign multiple sclerosis.

artículo científico publicado en 2008

Cognitive impairment predicts conversion to multiple sclerosis in clinically isolated syndromes

artículo científico publicado en 2009

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

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

artículo científico publicado en 2021

Complex repetitive behavior: punding after bilateral subthalamic nucleus stimulation in Parkinson's disease

artículo científico publicado en 2010

Coping strategies, psychological variables and their relationship with quality of life in multiple sclerosis.

artículo científico publicado en 2009

Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation

artículo científico publicado en 2019

Csf p-tau181/tau ratio as biomarker for TDP pathology in frontotemporal dementia

scholarly article by Barbara Borroni et al published 29 October 2014 in Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

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

Daytime course of sleepiness in de novo Parkinson's disease patients

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Development of human striatal anlagen after transplantation in a patient with Huntington's disease

artículo científico publicado en 2008

Differences in extracellular matrix production and basic fibroblast growth factor response in skin fibroblasts from sporadic and familial Alzheimer's disease

artículo científico publicado en 2007

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

artículo científico publicado en 2010

Double-Blind, Crossover, Placebo-Controlled Clinical Trial with L-Acetylcarnitine in Patients with Degenerative Cerebellar Ataxia

artículo científico publicado en 2000

Dramatic Reduction of Microemboli after Heparin Infusion in Progressing Stroke due to Aortic Arch Atheroma

artículo científico publicado en 2007

EFNS guidelines for the diagnosis and management of Alzheimer's disease.

artículo científico publicado en 2010

EFNS task force: the use of neuroimaging in the diagnosis of dementia.

artículo científico publicado en 2012

EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.

artículo científico publicado en 2012

EFNS-ENS/EAN Guideline on concomitant use of cholinesterase inhibitors and memantine in moderate to severe Alzheimer's disease

artículo científico

Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence.

artículo científico publicado en 2008

Education and occupation provide reserve in both ApoE ε4 carrier and noncarrier patients with probable Alzheimer's disease.

artículo científico publicado en 2011

Effect of phosphatidylserine on free radical susceptibility in human diploid fibroblasts

artículo científico publicado en 1993

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

artículo científico publicado en 2010

Energy metabolism in demented brain.

artículo científico publicado en 1986

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

artículo científico publicado en 2015

Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease ⬇️

artículo científico publicado el 1 de julio de 1995

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

article

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

artículo científico publicado en 2010

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

artículo científico publicado en 2011

FDG PET and the genetics of dementia

article

Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire (CCQ) across five European countries.

artículo científico publicado en 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

Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa

artículo científico publicado en 2012

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

Fibroblasts from FAD-linked presenilin 1 mutations display a normal unfolded protein response but overproduce Abeta42 in response to tunicamycin

artículo científico publicado en 2004

Fibroblasts from PS1 mutated pre-symptomatic subjects and Alzheimer's disease patients share a unique protein levels profile

artículo científico publicado en 2010

Fine specificity of antibodies against phospholipids and beta-2-glycoprotein I in monoclonal gammopathy associated neuropathies

artículo científico publicado en 2006

Folate, homocysteine, vitamin B12, and polymorphisms of genes participating in one-carbon metabolism in late-onset Alzheimer's disease patients and healthy controls

artículo científico publicado en 2011

Fragile X premutation with atypical symptoms at onset

artículo científico publicado en 2006

Free radical injury in skin cultured fibroblasts from Alzheimer's disease patients.

artículo científico publicado en 1992

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

artículo científico publicado en 2014

GAD antibodies associated neurological disorders: incidence and phenotype distribution among neurological inflammatory diseases.

artículo científico publicado en 2010

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships

artículo científico publicado en 2017

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

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

artículo científico publicado en 2015

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

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

article

Gluthatione level is altered in lymphoblasts from patients with familial Alzheimer's disease.

artículo científico publicado en 1999

Growth Properties and Growth Factor Responsiveness in Skin Fibroblasts from Centenarians

artículo científico publicado en 1998

HLA A2 allele is associated with age at onset of Alzheimer's disease.

artículo científico publicado en 1999

Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease

artículo científico publicado en 2005

Heterozygous TREM2 mutations in frontotemporal dementia

artículo científico

Higher uric acid serum levels are associated with better muscle function in the oldest old: Results from the Mugello Study

artículo científico publicado en 2017

How can elderly apolipoprotein E ε4 carriers remain free from dementia?

artículo científico publicado en 2012

Human herpesvirus 6-associated limbic encephalitis in adult recipients of unrelated umbilical cord blood transplantation

artículo científico publicado en 2008

Human longevity and 11p15.5: a study in 1321 centenarians

artículo científico publicado en 2009

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients

artículo científico publicado en 2014

IX Congresso Sindem: Italian Association for the study of Dementia linked to the Italian Neurological Society (SIN)

article

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

artículo científico publicado en 2003

IgM monoclonal gammopathy-associated neuropathies with different IgM specificity.

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Immunoproteasome and LMP2 polymorphism in aged and Alzheimer's disease brains

artículo científico publicado en 2006

Impact of cognitive impairment on coping strategies in multiple sclerosis

artículo científico publicado en 2009

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

Implication of α1-antichymotrypsin polymorphism in familial Alzheimer's disease

scientific article published on 01 March 1998

Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts

artículo científico publicado en 2006

Influence of apolipoprotein E epsilon4 genotype on brain tissue integrity in relapsing-remitting multiple sclerosis

artículo científico publicado en 2004

Influence of impaired T- and B-cell compartments on efficacy of IVIg in dysimmune neuropathies.

artículo científico publicado en 2007

Inherent abnormalities in oxidative metabolism in Alzheimer's disease: interaction with vascular abnormalities.

artículo científico publicado en 1997

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

artículo científico publicado en 2005

Interaction of caudate dopamine depletion and brain metabolic changes with cognitive dysfunction in early Parkinson's disease

article

Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner

artículo científico publicado en 2008

Interobserver agreement on Poser's and the new McDonald's diagnostic criteria for multiple sclerosis.

artículo científico publicado en 2003

Intravenous mitoxantrone and cyclophosphamide as second-line therapy in multiple sclerosis: an open-label comparative study of efficacy and safety

artículo científico publicado en 2008

Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy.

artículo científico publicado en 2014

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

article

Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis

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

Long-Term Adherence to Interferon β Therapy in Relapsing-Remitting Multiple Sclerosis

artículo científico publicado en 2007

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

artículo científico publicado en 2017

Low social interactions in eating disorder patients in childhood and adulthood: a multi-centre European case control study.

artículo científico publicado en 2012

Magnetic resonance imaging in Alzheimer's disease: from diagnosis to monitoring treatment effect.

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

artículo científico publicado en 2011

Metabolic correlates of executive dysfunction. Different patterns in mild and very mild Alzheimer's disease.

artículo científico publicado en 2007

Mild cognitive impairment: loss of linguistic task-induced changes in motor cortex excitability.

artículo científico publicado en 2009

Misserise mutation of S182 gene in Italian families with early-onset Alzheimer's disease

artículo científico publicado en 1995

Mitochondria and Alzheimer's disease

artículo científico publicado en 2012

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease

article

Monitoring Neuro-Motor Recovery From Stroke With High-Resolution EEG, Robotics and Virtual Reality: A Proof of Concept

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Multicenter standardized 18F-FDG PET diagnosis of mild cognitive impairment, Alzheimer's disease, and other dementias

artículo científico publicado en 2008

Music and cerebral hemodynamics.

artículo científico publicado en 2000

Mutant presenilin 1 increases the expression and activity of BACE1

artículo científico publicado en 2009

Mutation analysis of CHCHD10 in different neurodegenerative diseases

artículo científico publicado en 2015

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

artículo científico publicado en 2014

Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease

artículo científico publicado en 2008

Mutual information optimization for mass spectra data alignment

artículo científico publicado en 2011

Neocortical volume decrease in relapsing-remitting multiple sclerosis with mild cognitive impairment

artículo científico publicado en 2006

Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

artículo científico publicado en 2004

Neuropsychological and MRI measures predict short-term evolution in benign multiple sclerosis.

artículo científico publicado en 2009

Neutrophils CD11b and fibroblasts PGE(2) are elevated in Alzheimer's disease

artículo científico publicado en 2002

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

artículo científico publicado en 2007

No evidence of linkage between schizophrenia and D2 dopamine receptor gene locus in Italian pedigrees

article

No implication of apolipoprotein E polymorphism in Italian schizophrenic patients.

artículo científico publicado en 1998

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

article

Non-paraneoplastic limbic encephalitis associated with anti-glutamic acid decarboxylase antibodies

artículo científico publicado en 2008

Novel S-acyl glutathione derivatives prevent amyloid oxidative stress and cholinergic dysfunction in Alzheimer disease models

artículo científico publicado en 2012

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

artículo científico publicado en 2015

On the multivariate nature of brain metabolic impairment in Alzheimer's disease

artículo científico publicado en 2007

Orbitofrontal dysfunction related to both apathy and disinhibition in frontotemporal dementia

artículo científico publicado en 2006

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

artículo científico publicado en 2002

P53 codon 72 polymorphism and longevity: additional data on centenarians from continental Italy and Sardinia.

artículo científico publicado en 1999

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

artículo científico publicado en 2016

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

artículo científico publicado en 2007

Phospholipid composition and levels are not altered in fibroblasts bearing presenilin-1 mutations.

artículo científico publicado en 2000

Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease

artículo científico publicado en 2011

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

Predictive potential of pre-operative functional neuroimaging in patients treated with subthalamic stimulation

artículo científico publicado en 2010

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

artículo científico publicado en 2006

Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study.

artículo científico publicado en 2008

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 sleep disturbances in mild cognitive impairment and dementing disorders: a multicenter Italian clinical cross-sectional study on 431 patients.

artículo científico publicado en 2012

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

Protein tyrosine phosphatase receptor-type C exon 4 gene mutation distribution in an Italian multiple sclerosis population

artículo científico publicado en 2002

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

artículo científico publicado en 2015

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

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

Recommendations from the Italian Interdisciplinary Working Group (AIMN, AIP, SINDEM) for the utilization of amyloid imaging in clinical practice

artículo científico publicado en 2015

Recommendations of the Sleep Study Group of the Italian Dementia Research Association (SINDem) on clinical assessment and management of sleep disorders in individuals with mild cognitive impairment and dementia: a clinical review.

artículo científico

Regional cerebral metabolism in early Alzheimer's disease with clinically significant apathy or depression

artículo científico publicado en 2005

Reliability of administrative data for the identification of Parkinson's disease cohorts

artículo científico publicado en 2015

Response to interferon-beta therapy in relapsing-remitting multiple sclerosis: a comparison of different clinical criteria

article

Rethinking on the concept of biomarkers in preclinical Alzheimer's disease

artículo científico publicado en 2016

Risperidone in idiopathic and symptomatic dystonia: preliminary experience

artículo científico publicado en 2000

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease

artículo científico publicado en 2010

SAND: a Screening for Aphasia in NeuroDegeneration. Development and normative data

artículo científico publicado en 2017

Safety and tolerability of cyclophosphamide 'pulses' in multiple sclerosis: a prospective study in a clinical cohort.

artículo científico publicado en 2003

Semantic dementia associated with mutation V363I in the tau gene

artículo científico publicado en 2010

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Sleep and Cognitive Decline: A Strong Bidirectional Relationship. It Is Time for Specific Recommendations on Routine Assessment and the Management of Sleep Disorders in Patients with Mild Cognitive Impairment and Dementia

artículo científico

Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference

artículo científico publicado en 2011

Spectrophotometric measurement of pyruvate dehydrogenase complex activity in cultured human fibroblasts

artículo científico publicado en 1981

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 C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease.

artículo científico publicado en 2001

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients

artículo científico publicado en 2015

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

artículo científico publicado en 2010

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

artículo científico publicado en 2012

The contribution of cerebrospinal fluid oligoclonal bands to the early diagnosis of multiple sclerosis.

artículo científico publicado en 2009

The diagnosis of dementias: a practical tool not to miss rare causes

artículo científico publicado en 2017

The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death.

artículo científico publicado en 2004

The effect of tetraethylammonium on intracellular calcium concentration in Alzheimer's disease fibroblasts with APP, S182 and E5-1 missense mutations.

artículo científico publicado en 1996

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

artículo científico publicado en 2007

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

Tissue banking and EURAGE

artículo científico publicado en 1989

Toward the validation of functional neuroimaging as a potential biomarker for Alzheimer's disease: implications for drug development

artículo científico publicado en 2005

Uncommon Dementias

Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation

artículo científico publicado en 2003

Which target for DBS in Parkinson's disease? Subthalamic nucleus versus globus pallidus internus

artículo científico publicado en 2001

White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

artículo científico publicado en 2017

Yawning: a behavioural marker of sleepiness in de novo PD patients

artículo científico publicado en 2013

p66(shc) is highly expressed in fibroblasts from centenarians.

artículo científico publicado en 2005

α2-Macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease

article

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