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Lista de obras de Elio Scarpini

+10 T/C polymorphisms in the gene of transforming growth factor-β1 are associated with neurodegeneration and its clinical evolution

article

A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation

artículo científico publicado en 2012

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

A functional variant in ERAP1 predisposes to multiple sclerosis

artículo científico publicado en 2012

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 polymorphism in SEL1L confers susceptibility to Alzheimer's disease

artículo científico publicado en 2006

A novel study and meta-analysis of the genetic variation of the serotonin transporter promoter in the italian population do not support a large effect on Alzheimer's disease risk

artículo científico publicado en 2011

A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk

artículo científico publicado en 2008

A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease

artículo científico publicado en 2009

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

artículo científico publicado en 2012

APOE and Alzheimer disease: a major gene with semi-dominant inheritance

artículo científico publicado en 2011

Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration.

artículo científico publicado en 2009

Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration

artículo científico publicado en 2006

Acute ataxia coincident with seroconversion for anti-HIV

article

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

Alpha-MSH peptides inhibit production of nitric oxide and tumor necrosis factor-alpha by microglial cells activated with beta-amyloid and interferon gamma

artículo científico publicado en 1999

Alpha1-antichymotrypsin induces TNF-alpha production and NF-kappaB activation in the murine N9 microglial cell line

artículo científico publicado en 2009

Alzheimer's Disease Diagnosis: Discrepancy between Clinical, Neuroimaging, and Cerebrospinal Fluid Biomarkers Criteria in an Italian Cohort of Geriatric Outpatients: A Retrospective Cross-sectional Study.

artículo científico publicado en 2017

Alzheimer's disease: from molecular pathogenesis to innovative therapies.

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 emerging role for long non-coding RNA dysregulation in neurological disorders

artículo científico publicado en 2013

Analysis of the genes coding for subunit 10 and 15 of cytochrome c oxidase in Alzheimer's disease

artículo científico publicado en 2009

Anti-GM2 IgM antibodies: clinical correlates and reactivity with a human neuroblastoma cell line.

artículo científico publicado en 1999

Appearance and localization of dystrophin in normal human fetal muscle

artículo científico publicado en 1991

Appearance of PLP mRNA in specific regions of the developing rat lumbosacral spinal cord as revealed by in situ hybridization

scientific article published on 01 May 1993

Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects

article

Association of a NOS1 promoter repeat with Alzheimer's disease

artículo científico publicado en 2007

Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.

artículo científico publicado en 2005

Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy

artículo científico publicado en 2008

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 haematopoietic stem cell transplantation with an intermediate intensity conditioning regimen in multiple sclerosis: the Italian multi-centre experience

article

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

artículo científico publicado en 2013

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

scientific article published on 01 January 2011

Balò's concentric sclerosis: still to be considered as a variant of multiple sclerosis?

artículo científico publicado en 2015

Behavioral and Neurophysiological Effects of Transcranial Direct Current Stimulation (tDCS) in Fronto-Temporal Dementia ⬇️

artículo científico publicado en 2018

Binge eating and fast cognitive worsening in an early-onset bvFTD patient carrying C9ORF72 expansion

artículo científico publicado en 2014

Body Mass Index Predicts Progression of Mild Cognitive Impairment to Dementia.

artículo científico publicado en 2016

Brain temperature in multiple sclerosis

artículo científico publicado en 2013

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

artículo científico publicado en 2013

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

artículo científico publicado en 2013

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

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

CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease

artículo científico publicado en 2004

CHF5074 reduces biomarkers of neuroinflammation in patients with mild cognitive impairment: a 12-week, double-blind, placebo-controlled study.

artículo científico publicado en 2013

CHRNA7 Gene and Response to Cholinesterase Inhibitors in an Italian Cohort of Alzheimer's Disease Patients.

artículo científico publicado en 2016

CSF β-amyloid and white matter damage: a new perspective on Alzheimer's disease

artículo científico publicado en 2017

CSF β-amyloid as a putative biomarker of disease progression in multiple sclerosis

artículo científico publicado en 2016

CSF β-amyloid predicts prognosis in patients with multiple sclerosis

artículo científico publicado en 2018

CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical course

artículo científico publicado en 2007

Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease

article

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

artículo científico publicado en 2007

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

artículo científico publicado en 2009

Candidate gene analysis of semaphorins in patients with Alzheimer's disease.

artículo científico publicado en 2009

Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease.

artículo científico publicado en 2010

Cerebrospinal Fluid Level of Aquaporin4: A New Window on Glymphatic System Involvement in Neurodegenerative Disease?

scientific article published on 01 January 2019

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

artículo científico publicado en 2011

Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes

artículo científico publicado en 2009

Cessation versus continuation of galantamine treatment after 12 months of therapy in patients with Alzheimer's disease: a randomized, double blind, placebo controlled withdrawal trial.

artículo científico publicado en 2011

Chemokine network in multiple sclerosis: role in pathogenesis and targeting for future treatments

artículo científico publicado en 2004

Chemokines in serum and cerebrospinal fluid of Alzheimer's disease patients.

artículo científico publicado en 2003

Chitinase 3-like 1: prognostic biomarker in clinically isolated syndromes

artículo científico publicado en 2015

Circulating miRNAs as potential biomarkers in Alzheimer's disease

artículo científico publicado en 2014

Clinical features of Sjogren’s syndrome in patients with multiple sclerosis

artículo científico publicado en 2010

Clinical phenotypes and genetic biomarkers of FTLD.

artículo científico publicado en 2012

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

Comparison of β2-microglobulin serum level between Alzheimer's patients, cognitive healthy and mild cognitive impaired individuals.

artículo científico publicado en 2018

Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study.

artículo científico publicado en 2015

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

Cultured human monocytes release proinflammatory cytokines in response to myelin basic protein

scientific article published on 01 August 1998

Cultures of human Schwann cells isolated from fetal nerves

artículo científico publicado en 1988

Cytochrome c oxidase during human fetal development.

artículo científico publicado en 1989

Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy

artículo científico publicado en 1986

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

artículo científico publicado en 2009

DNA methylation in repetitive elements and Alzheimer disease

artículo científico publicado en 2011

Decrease of nerve Na+,K(+)-ATPase activity in the pathogenesis of human diabetic neuropathy

artículo científico publicado en 1993

Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis.

artículo científico publicado en 2013

Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions

artículo científico publicado en 2014

Detection of misfolded Aβ oligomers for sensitive biochemical diagnosis of Alzheimer's disease

artículo científico publicado en 2014

Disease-modifying drugs in Alzheimer's disease

scientific article published on 06 December 2013

Disease-modifying drugs in multiple sclerosis: new oral options

Disease-modifying treatments for Alzheimer's disease

artículo científico publicado en 2011

Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales.

artículo científico publicado en 2018

Does Vascular Burden Contribute to the Progression of Mild Cognitive Impairment to Dementia?

artículo científico publicado en 2012

E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosis

artículo científico publicado en 2005

Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations

artículo científico publicado en 2012

Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels in patients with multiple sclerosis

artículo científico publicado en 2016

Effect of rivastigmine on delay to diagnosis of Alzheimer's disease from mild cognitive impairment: the InDDEx study

artículo científico publicado en 2007

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

artículo científico publicado en 2017

Efficacy of Souvenaid in mild Alzheimer's disease: results from a randomized, controlled trial

artículo científico publicado en 2012

Emerging amyloid disease-modifying drugs for Alzheimer's disease.

artículo científico publicado en 2016

Endovascular treatment of CCSVI in patients with multiple sclerosis: clinical outcome of 462 cases.

artículo científico publicado en 2013

Epigenetic modulation of BDNF gene in patients with major depressive disorder.

artículo científico publicado en 2012

Epigenetic modulation of BDNF gene: differences in DNA methylation between unipolar and bipolar patients

artículo científico publicado en 2014

Epigenetic regulation of fatty acid amide hydrolase in Alzheimer disease

artículo científico publicado en 2012

Epigenetic regulatory modifications in genetic and sporadic frontotemporal dementia

scientific article published on 05 June 2018

Erratum to: Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay

artículo científico publicado en 2016

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

article

Establishment of Schwann cell cultures from adult rat peripheral nerves

artículo científico publicado en 1988

Estrogens need insulin-like growth factor I cooperation to exert their neuroprotective effects in post-menopausal women

artículo científico publicado en 2012

Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation.

artículo científico publicado en 2017

Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism†

scientific article published on 01 January 2014

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

artículo científico publicado en 2011

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

artículo científico publicado en 2013

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

artículo científico publicado en 2011

Expression of nerve growth factor receptor during human peripheral nerve development

artículo científico publicado en 1988

Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease.

artículo científico publicado en 2013

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

Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration

artículo científico publicado en 2010

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

artículo científico publicado en 2011

Frontotemporal Lobar Degeneration

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

artículo científico publicado en 2014

Frontotemporal lobar degeneration: current knowledge and future challenges.

artículo científico

GRN Thr272fs clinical heterogeneity: a case with atypical late onset presenting with a dementia with Lewy bodies phenotype

artículo científico publicado en 2013

GRN variability contributes to sporadic frontotemporal lobar degeneration

artículo científico publicado en 2010

GSK3β genetic variability in patients with Multiple Sclerosis

artículo científico publicado en 2011

Gender effects on plasma PGRN levels in patients with Alzheimer's disease: a preliminary study

artículo científico publicado en 2013

Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis

artículo científico publicado en 2007

Gene promoter methylation and expression of Pin1 differ between patients with frontotemporal dementia and Alzheimer's disease.

artículo científico publicado en 2016

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 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 risk factors for the posterior cortical atrophy variant of Alzheimer's disease

artículo científico publicado en 2016

Genetic variation in the choline O-acetyltransferase gene in depression and Alzheimer's disease: the VITA and Milano studies

artículo científico publicado en 2011

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

Genetics of frontotemporal lobar degeneration.

artículo científico publicado en 2012

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

artículo científico publicado en 2012

Growth Arrest Specific 6 Concentration is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's Disease.

artículo científico publicado en 2017

HLA-class I markers and multiple sclerosis susceptibility in the Italian population

artículo científico publicado en 2009

Heparan sulfate proteoglycan induces the production of NO and TNF-alpha by murine microglia

artículo científico publicado en 2005

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

artículo científico publicado en 2005

Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene

artículo científico publicado en 2011

Heterozygous TREM2 mutations in frontotemporal dementia

artículo científico

ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution

article

IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease.

artículo científico publicado en 2007

Idalopirdine as a treatment for Alzheimer's disease

artículo científico publicado en 2015

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

artículo científico publicado en 2011

Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay

artículo científico publicado en 2015

Identification of soluble TREM-2 in the cerebrospinal fluid and its association with multiple sclerosis and CNS inflammation

artículo científico publicado en 2008

Immunocytochemical expression of human muscle cell p75 neurotrophin receptor is down-regulated by cyclic adenosine 3',5'-monophosphate

scientific article published on 01 October 1997

Immunological patterns identifying disease course and evolution in multiple sclerosis patients

Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population

artículo científico publicado en 2010

Immunotherapy against amyloid pathology in Alzheimer's disease

artículo científico publicado en 2013

Improved Cerebrospinal Fluid-Based Discrimination between Alzheimer's Disease Patients and Controls after Correction for Ventricular Volumes

artículo científico publicado en 2017

In situ hybridization study of myelin protein mRNA in rats with an experimental diabetic neuropathy

artículo científico publicado en 1996

Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects

artículo científico publicado en 2014

Inducible nitric oxide synthase (iNOS) in immune-mediated demyelination and Wallerian degeneration of the rat peripheral nervous system

artículo científico publicado en 2004

Induction of adhesion molecules on human schwann cells by proinflammatory cytokines, an immunofluorescence study

artículo científico publicado en 1999

Induction of p75NGFR in human diabetic neuropathy

artículo científico publicado en 1996

Inflammatory molecules in Frontotemporal Dementia: cerebrospinal fluid signature of progranulin mutation carriers.

artículo científico publicado en 2015

Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients

artículo científico publicado en 2005

Innate immune system and inflammation in Alzheimer's disease: from pathogenesis to treatment

artículo científico publicado en 2014

Intensive versus standard lowering of blood pressure in the acute phase of intracranial haemorrhage: a systematic review and meta-analysis.

artículo científico publicado en 2017

Interaction between the APOE epsilon4 allele and the APH-1b c + 651T > G SNP in Alzheimer's disease.

artículo científico publicado en 2007

Interleukin-1 beta and interferon-gamma induce proliferation and apoptosis in cultured Schwann cells.

artículo científico publicado en 2002

Interleukin-6 plasma level increases with age in an Italian elderly population ("The Treviso Longeva"-Trelong-study) with a sex-specific contribution of rs1800795 polymorphism

artículo científico publicado en 2009

Intrathecal chemokine levels in Alzheimer disease and frontotemporal lobar degeneration.

artículo científico publicado en 2006

Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer disease

artículo científico publicado en 2006

Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2008

Inverse agonism of cannabinoid CB1 receptor blocks the adhesion of encephalitogenic T cells in inflamed brain venules by a protein kinase A-dependent mechanism.

artículo científico publicado en 2011

Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway?

artículo científico publicado en 2015

Is HCRTR2 a genetic risk factor for Alzheimer's disease?

artículo científico publicado en 2014

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

artículo científico publicado en 2010

Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis

artículo científico publicado en 2005

Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?

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

Lack of Association between the GPR3 Gene and the Risk for Alzheimer's Disease

artículo científico publicado en 2011

Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort

artículo científico publicado en 2010

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

scientific article published on 27 August 2018

Loss of epidermal growth factor regulation by cobalamin in multiple sclerosis

artículo científico publicado en 2010

Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patients

artículo científico publicado en 2011

Low-affinity nerve growth factor receptor expression in sciatic nerve during P2-peptide induced experimental allergic neuritis

scientific article published on 01 October 1995

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels

artículo científico publicado en 2009

MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.

artículo científico publicado en 2004

MDC/CCL22 intrathecal levels in patients with multiple sclerosis.

artículo científico publicado en 2008

Manifesting carrier of X-linked Duchenne muscular dystrophy

artículo científico publicado en 1981

Merkel cell carcinoma in a patient with relapsing-remitting multiple sclerosis treated with fingolimod

artículo científico publicado en 2017

MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers

artículo científico publicado en 2011

MicroRNAs as active players in the pathogenesis of multiple sclerosis

artículo científico

Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset

artículo científico publicado en 2019

Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases

artículo científico publicado en 1994

Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid

artículo científico publicado en 2011

Muscular carnitine synthesis and palmitate metabolism in vitro

artículo científico publicado en 1978

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.

artículo científico publicado en 2011

Myelin protein transcripts increase in experimental diabetic neuropathy

artículo científico publicado en 1993

Myopathy with paroxysmal myoglobinuria and focal muscle necrosis following enfluorane anaesthesia

artículo científico publicado en 1978

NOTCH3 gene mutations in subjects clinically suspected of CADASIL.

artículo científico publicado en 2011

Neurofilament light chain: a biomarker for genetic frontotemporal dementia

scientific article published on July 2016

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration

artículo científico publicado en 2007

No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis

scientific article published on 16 April 2014

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort

artículo científico publicado en 2009

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

artículo científico publicado en 2016

Novel evidence of phenotypical variability in the hexanucleotide repeat expansion in chromosome 9.

artículo científico

Novel exon 1 progranulin gene variant in Alzheimer's disease.

artículo científico

Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia

artículo científico publicado en 2013

Old and new acetylcholinesterase inhibitors for Alzheimer's disease

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Osteopontin is increased in the cerebrospinal fluid of patients with Alzheimer's disease and its levels correlate with cognitive decline.

artículo científico publicado en 2010

Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's disease

artículo científico publicado en 2005

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis

artículo científico publicado en 2005

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

artículo científico publicado en 2016

Partial recovery after severe immune reconstitution inflammatory syndrome in a multiple sclerosis patient with progressive multifocal leukoencephalopathy

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

Pharmacological Management of Psychiatric Symptoms in Frontotemporal Dementia: A Systematic Review

artículo científico publicado en 2017

Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred

article

Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficits

artículo científico

Physical activity reduces the risk of dementia in mild cognitive impairment subjects: a cohort study

artículo científico publicado en 2014

Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease.

artículo científico publicado en 2012

Pioglitazone for the treatment of Alzheimer's disease

artículo científico publicado en 2016

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes

artículo científico publicado en 2016

Plasma levels of beta-amyloid (1-42) in Alzheimer's disease and mild cognitive impairment.

artículo científico publicado en 2006

Polymorphisms in the LOC387715/ARMS2 putative gene and the risk for Alzheimer's disease.

artículo científico publicado en 2008

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

Possible association between SNAP-25 single nucleotide polymorphisms and alterations of categorical fluency and functional MRI parameters in Alzheimer's disease

artículo científico publicado en 2014

Possible influence of a non-synonymous polymorphism located in the NGF precursor on susceptibility to late-onset Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2012

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

Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration.

artículo científico publicado en 2008

Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population.

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

Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosis

artículo científico publicado en 2005

Profiling of Specific Gene Expression Pathways in Peripheral Cells from Prodromal Alzheimer's Disease Patients.

artículo científico publicado en 2018

Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutations

artículo científico publicado en 2015

Progranulin as a therapeutic target for dementia

scientific article published on 22 June 2018

Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration

artículo científico publicado en 2012

Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

artículo científico publicado en 2012

Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males

article

Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder

artículo científico publicado en 2014

Progranulin genetic polymorphisms influence progression of disability and relapse recovery in multiple sclerosis

artículo científico publicado en 2015

Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series

article

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

artículo científico publicado en 2009

Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

artículo científico publicado en 2017

Progress in Alzheimer's disease

artículo científico publicado en 2011

Progress in Alzheimer's disease research in the last year

artículo científico publicado en 2013

Progress in multiple sclerosis research in the last year

artículo científico publicado en 2012

Progressive, isolated language disturbance: its significance in a 65-year-old-man. A case report with implications for treatment and review of literature

artículo científico publicado en 2005

Proinflammatory profile of cytokine production by human monocytes and murine microglia stimulated with beta-amyloid[25-35].

artículo científico publicado en 1999

Prolonged visual memory enhancement after direct current stimulation in Alzheimer's disease

artículo científico publicado en 2011

Psychiatric symptoms in frontotemporal dementia: epidemiology, phenotypes, and differential diagnosis.

artículo científico publicado en 2015

Rapid quantitative immunohistochemical assessment of human peripheral neuropathies using a monoclonal antibody against nerve growth factor receptor

scientific article published on 01 December 1989

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Recognition of viral and self-antigens by TH1 and TH1/TH17 central memory cells in patients with multiple sclerosis reveals distinct roles in immune surveillance and relapses

artículo científico publicado en 2017

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

artículo científico publicado en 2020

Regulatory T cells suppress the late phase of the immune response in lymph nodes through P-selectin glycoprotein ligand-1.

artículo científico publicado en 2013

Repetitive element hypermethylation in multiple sclerosis patients.

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Reversible Mild Cognitive Impairment: The Role of Comorbidities at Baseline Evaluation.

artículo científico publicado en 2016

RhoA and zeta PKC control distinct modalities of LFA-1 activation by chemokines: critical role of LFA-1 affinity triggering in lymphocyte in vivo homing

artículo científico publicado en 2004

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

artículo científico publicado en 2011

Role of VEGF gene variability in longevity: A lesson from the Italian population

article

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

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

artículo científico publicado en 2009

S-100 protein and laminin: Immunocytochemical markers for human Schwann cells in vitro

scientific article published on 01 July 1986

SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis

scientific article published on 27 October 2005

SORL1 Gene is Associated with the Conversion from Mild Cognitive Impairment to Alzheimer's Disease

artículo científico publicado en 2015

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

artículo científico publicado en 2012

Safety of MF59-adjuvanted influenza vaccination in the elderly: results of a comparative study of MF59-adjuvanted vaccine versus nonadjuvanted influenza vaccine in northern Italy.

artículo científico publicado en 2013

Schwann cell undergoes apoptosis during experimental allergic neuritis (EAN)

artículo científico publicado en 1998

Sciatic endometriosis presenting as periodic (catamenial) sciatic radiculopathy

artículo científico publicado en 2012

Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia

artículo científico publicado en 2012

Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII.

artículo científico publicado en 2012

Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy

artículo científico publicado en 2009

Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease

artículo científico publicado en 2005

Serum folate concentrations in patients with cortical and subcortical dementias

artículo científico publicado en 2007

Severe polyneuropathy in a patient with Churg-Strauss syndrome

artículo científico publicado en 2000

Structural and metabolic cerebral alterations between elderly bipolar disorder and behavioural variant frontotemporal dementia: A combined MRI-PET study

artículo científico publicado en 2018

Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease

artículo científico publicado en 2009

Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy

artículo científico publicado en 1992

Testing the 2018 NIA-AA research framework in a retrospective large cohort of patients with cognitive impairment: from biological biomarkers to clinical syndromes

artículo científico publicado en 2019

The Alzheimer's Association external quality control program for cerebrospinal fluid biomarkers

artículo científico publicado en 2011

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 CST3 B haplotype is associated with frontotemporal lobar degeneration.

artículo científico publicado en 2009

The Enigmatic Role of Viruses in Multiple Sclerosis: Molecular Mimicry or Disturbed Immune Surveillance?

artículo científico publicado en 2017

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

artículo científico publicado en 2010

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration

artículo científico publicado en 2009

The Neuroanatomy of Somatoform Disorders: A Magnetic Resonance Imaging Study

artículo científico publicado en 2018

The Progranulin (GRN) Cys157LysfsX97 Mutation is Associated with Nonfluent Variant of Primary Progressive Aphasia Clinical Phenotype

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

artículo científico publicado en 2012

The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.

artículo científico publicado en 2005

The expression of CD59 in experimental allergic neuritis

artículo científico publicado en 1999

The functional MAOA-uVNTR promoter polymorphism in patients with frontotemporal dementia

artículo científico publicado en 2008

The human astrocytoma cell line U373MG produces monocyte chemotactic protein (MCP)-1 upon stimulation with beta-amyloid protein.

artículo científico publicado en 2000

The impact of osteopontin gene variations on multiple sclerosis development and progression

artículo científico publicado en 2012

The leukocyte expression of CD36 is low in patients with Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2006

The loss of macular ganglion cells begins from the early stages of disease and correlates with brain atrophy in multiple sclerosis patients

artículo científico publicado en 2017

The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia

artículo científico publicado en 2015

The ontogenesis of Fc gamma receptors and complement receptors CR1 in human peripheral nerve

artículo científico publicado en 1990

The results of two multicenter, open-label studies assessing efficacy, tolerability and safety of protiramer, a high molecular weight synthetic copolymeric mixture, in patients with relapsing-remitting multiple sclerosis.

artículo científico publicado en 2008

The role of the innate immune system in Alzheimer's disease and frontotemporal lobar degeneration: an eye on microglia

artículo científico publicado en 2013

The serotonin transporter promoter polymorphic region is not a risk factor for Alzheimer's disease related behavioral disturbances.

artículo científico publicado en 2009

The urokinase-type plasminogen activator polymorphism PLAU_1 is a risk factor for APOE-epsilon4 non-carriers in the Italian Alzheimer's disease population and does not affect the plasma Abeta(1-42) level.

artículo científico publicado en 2006

Tolerability and safety of Souvenaid in patients with mild Alzheimer's disease: results of multi-center, 24-week, open-label extension study

artículo científico publicado en 2015

Transcranial Direct Current Stimulation Modulates Cortical Neuronal Activity in Alzheimer's Disease

artículo científico publicado en 2016

Transcranial direct current stimulation (tDCS) for fatigue in multiple sclerosis.

artículo científico publicado en 2014

Transcranial direct current stimulation improves recognition memory in Alzheimer disease.

artículo científico publicado en 2008

Transmembrane protein 106B gene (TMEM106B) variability and influence on progranulin plasma levels in patients with Alzheimer's disease.

artículo científico publicado en 2015

Treatment of Alzheimer's disease: current status and new perspectives.

artículo científico publicado en 2003

Treatment of Alzheimer's disease: symptomatic and disease-modifying approaches

artículo científico publicado en 2010

Usefulness of Multi-Parametric MRI for the Investigation of Posterior Cortical Atrophy

artículo científico publicado en 2015

VEGF genetic variability is associated with increased risk of developing Alzheimer's disease

artículo científico publicado en 2009

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

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Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition

artículo científico publicado en 2008

Variations of the perforin gene in patients with multiple sclerosis

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Vascular endothelial growth factor gene variability is associated with increased risk for AD.

artículo científico publicado en 2005

Visual loss and enlarged extraocular muscles from metastatic signet ring carcinoma

artículo científico publicado en 2001

Weight Loss Predicts Progression of Mild Cognitive Impairment to Alzheimer's Disease.

artículo científico publicado en 2016

Word and Picture Version of the Free and Cued Selective Reminding Test (FCSRT): Is There Any Difference?

artículo científico publicado en 2017

p75 neurotrophin receptor induction and macrophage infiltration in peripheral nerve during experimental diabetic neuropathy: possible relevance on regeneration.

artículo científico publicado en 1997

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