List of works by Daniela Galimberti

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

scientific article published on 31 October 2012

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

A Case with Early Onset Alzheimer's Disease, Frontotemporal Hypometabolism, ApoE Genotype ɛ4/ɛ4 and C9ORF72 Intermediate Expansion: A Treviso Dementia (TREDEM) Registry Case Report

scientific article published on 01 January 2019

A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms Status

scientific article published on 20 October 2016

A case of bipolar disorder developing into atypical parkinsonism and presenting with frontotemporal asymmetrical brain degeneration. A TREDEM Registry Case Report

scientific article published on 18 February 2020

A functional variant in ERAP1 predisposes to multiple sclerosis

scientific article

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

scientific article

A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD.

scientific article published on 16 April 2013

A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort

scientific article published on 05 February 2020

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

scientific article

A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia

scientific article published on 11 October 2017

A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease

scientific article

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

scientific article

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

scientific article

A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy

article

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

scientific article

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

scientific article published on 6 January 2012

ABCA1- and ABCG1-mediated cholesterol efflux capacity of cerebrospinal fluid is impaired in Alzheimer's disease

scientific article published on 05 June 2019

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

scientific article

APOE ε2 and ε4 influence the susceptibility for Alzheimer's disease but not other dementias

scientific article published on 5 April 2010

Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort

scientific article published on 05 August 2020

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

scientific article

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

scientific article published on 07 November 2006

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

scientific article published on September 1999

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

scientific article published on October 2009

Alzheimer's disease: from pathogenesis to disease-modifying approaches

scientific article

Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis: correlation with CSF β-amyloid levels and brain volumes

article

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

scientific article published in January 2011

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

scientific article published on 14 October 2013

Analysis of brain atrophy and local gene expression in genetic frontotemporal dementia

scientific article published on 01 July 2020

Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis.

scientific article published on 12 January 2015

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

scientific article published on 29 September 2013

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

scientific article

Anti-Cholinergic Derangement of Cortical Metabolism on 18F-FDG PET in a Patient with Frontotemporal Lobar Degeneration Dementia: A Case of the TREDEM Registry

scientific article published on 02 March 2020

Apathy in presymptomatic genetic frontotemporal dementia predicts cognitive decline and is driven by structural brain changes

scientific article published on 14 December 2020

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans

scientific article published on 13 October 2012

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

scientific article

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

scientific article

Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population

scientific article published on 18 December 2021

Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population

article

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

scientific article published on 20 November 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

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

scientific article

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?

scientific article

Behavioral genetics of neurodegenerative disorders

scientific article published on January 2012

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

scientific article

Biomarkers and phenotypic expression in Alzheimer's disease: exploring the contribution of frailty in the Alzheimer's Disease Neuroimaging Initiative

scientific article published on 19 November 2020

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

scientific article published on 31 March 2016

Brain functional network integrity sustains cognitive function despite atrophy in presymptomatic genetic frontotemporal dementia

scientific article published on 20 November 2020

Brain temperature in multiple sclerosis

scientific article published on 24 October 2013

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

scientific article published on 16 December 2013

C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone

scientific article published on 21 August 2019

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

scientific article

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

scientific article

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

scientific article (publication date: August 2009)

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

scientific article published in October 2004

CEREBRAL PERFUSION AS AN IMAGING BIOMARKER OF PRESYMPTOMATIC GENETIC FRONTOTEMPORAL DEMENTIA: PRELIMINARY RESULTS FROM THE GENETIC FRONTOTEMPORAL DEMENTIA INITIATIVE (GENFI)

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

scientific article published on 8 January 2015

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

scientific article

CLIC1 Protein Accumulates in Circulating Monocyte Membrane during Neurodegeneration

scientific article published on 21 February 2020

CSF pro-orexin and amyloid-β38 expression in Alzheimer's disease and frontotemporal dementia

scientific article published on 25 August 2018

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

scientific article published on 20 October 2017

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

scientific article published on 17 October 2016

CSF β-amyloid predicts early cerebellar atrophy and is associated with a poor prognosis in multiple sclerosis

scientific article published on 21 October 2019

CSF β-amyloid predicts prognosis in patients with multiple sclerosis

scientific article published on 07 August 2018

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

scientific article

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

scientific article

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

scientific article published on 25 February 2009

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

scientific article published on 3 December 2009

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

scientific article

Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study

scientific article published on 01 April 2019

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.

scientific article published in January 2011

Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes

scientific article

Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status

scientific article published on 11 January 2016

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

scientific article

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

scientific article published in April 2003

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

scientific article published on 13 February 2015

Circulating miRNAs as potential biomarkers in Alzheimer's disease

scientific article

Clinical and MRI correlates of disease progression in a case of nonfluent/agrammatic variant of primary progressive aphasia due to progranulin (GRN) Cys157LysfsX97 mutation

scientific article published on 12 April 2014

Clinical phenotypes and genetic biomarkers of FTLD.

scientific article

Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia

scientific article published on 23 May 2019

Clinical, neuropathological, and genetic characteristics of the novel IVS9+1delG GRN mutation in a patient with frontotemporal dementia

scientific article published in January 2012

Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study

scientific article

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

scientific article (publication date: May 2011)

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

scientific article published on 7 June 2021

Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI).

scientific article

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

scientific article published on 9 May 2018

Consensus definitions and application guidelines for control groups in cerebrospinal fluid biomarker studies in multiple sclerosis

scientific article published on 21 May 2013

Consensus guidelines for lumbar puncture in patients with neurological diseases

scientific article

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

scientific article

Corneal involvement in rheumatoid arthritis: an in vivo confocal study

scientific article

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

Current understanding on the role of standard and immunoproteasomes in inflammatory/immunological pathways of multiple sclerosis

scientific article published on 02 January 2014

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

scientific article

DNA methylation in repetitive elements and Alzheimer disease

scientific article published on 03 February 2011

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

scientific article published in December 2013

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

scientific article published on 28 June 2014

Dementia: not only Alzheimer's disease, an eye on frontotemporal dementia.

scientific article

Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis

scholarly article published in February 2024

Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic Syndrome

scientific article published on 02 December 2020

Differentiating Vogt-Koyanagi-Harada syndrome from recurrent optic neuritis: a case report and review of the literature concerning Hispanic patients

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

scientific article

Disease-related cortical thinning in presymptomatic granulin mutation carriers

scientific article published on 29 December 2020

Disease-specific plasma levels of mitokines FGF21, GDF15, and Humanin in type II diabetes and Alzheimer's disease in comparison with healthy aging

scientific article published on 31 October 2020

Distinct Neuroanatomical Correlates of Neuropsychiatric Symptoms in the Three Main Forms of Genetic Frontotemporal Dementia in the GENFI Cohort

scientific article published on 01 January 2018

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

scientific article

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

scientific article published on 10 November 2012

Downregulation of exosomal miR-204-5p and miR-632 as a biomarker for FTD: a GENFI study

scientific article published on 6 February 2018

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

scientific article

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

scientific article published on 25 March 2015

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

scientific article published in January 2012

Early symptoms in symptomatic and preclinical genetic frontotemporal lobar degeneration

scientific article published on 07 August 2020

Education modulates brain maintenance in presymptomatic frontotemporal dementia

scientific article published on 10 June 2019

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

scientific article

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

scientific article published on 23 January 2017

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

scientific article

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

scientific article

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

scientific article

Epigenetic regulation of fatty acid amide hydrolase in Alzheimer disease

scientific article

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

scientific article published on 23 February 2016

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

article

Estimating the inheritance of frontotemporal lobar degeneration in the Italian population

scientific article published on January 2014

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

scientific article published on 22 March 2012

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

scientific article published on 15 November 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 retinal anterograde neurodegeneration in the very early stages of multiple sclerosis: a longitudinal OCT study

scientific article published on 30 April 2020

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

scientific article

Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases

scientific article published on 28 August 2019

Exploring the role of BDNF DNA methylation and hydroxymethylation in patients with obsessive compulsive disorder

scientific article published on 06 April 2019

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

scientific article published on 25 February 2013

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

scientific article published on 19 August 2011

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

scientific article published in January 2013

Extracellular proteasome-osteopontin circuit regulates cell migration with implications in multiple sclerosis

scientific article published on 09 March 2017

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

scientific article

Familial clustering in Italian progressive-onset and bout-onset multiple sclerosis

scientific article published on 11 February 2014

Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers

scientific article published on 14 April 2020

Fluid biomarkers in frontotemporal dementia: past, present and future

scientific article published on 13 November 2020

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

scientific article published on 13 October 2010

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

scientific article published in January 2011

Frontotemporal Dementia Misdiagnosed for Post-Treatment Lyme Disease Syndrome or vice versa? A Treviso Dementia (TREDEM) Registry Case Report

scientific article published on 01 January 2018

Frontotemporal Lobar Degeneration

Frontotemporal Lobar Degeneration: Genetics and Clinical Phenotypes

article

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

scientific article

Frontotemporal dementia: correlations between psychiatric symptoms and pathology

scientific article published on 12 April 2020

Frontotemporal lobar degeneration: current knowledge and future challenges.

scientific article published on 25 April 2012

Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia

scientific article published on 04 January 2019

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

scientific article published in January 2013

GRN variability contributes to sporadic frontotemporal lobar degeneration

scientific article

GSK3β genetic variability in patients with Multiple Sclerosis

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients

article

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

scientific article published on 28 February 2019

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

scientific article

Genetic risk factors and role of immune dysfunction in FTLD

scientific article published on 01 May 2019

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

scientific article published on 15 March 2016

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

scientific article published on 02 September 2020

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

scientific article

Genetics and biology of Alzheimer's disease and frontotemporal lobar degeneration

scientific article

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

scientific article published in January 2012

Genetics of frontotemporal lobar degeneration.

scientific article published on 10 April 2012

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

scientific article (publication date: October 2009)

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

scientific article published on 20 March 2012

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

scientific article

Guidelines for uniform reporting of body fluid biomarker studies in neurologic disorders

scientific article published on 22 August 2014

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

scientific article

Hemodynamic and Anatomic Variations Require an Adaptable Approach during Intra-Arterial Chemotherapy for Intraocular Retinoblastoma: Alternative Routes, Strategies, and Follow-Up.

scientific article published on 25 February 2016

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

scientific article published on 24 July 2011

Heterozygous TREM2 mutations in frontotemporal dementia

scientific article published on 16 October 2013

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

scientific article published on 6 June 2014

ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution

article

IL-33 and its decoy sST2 in patients with Alzheimer's disease and mild cognitive impairment

scientific article published on 06 June 2020

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

scientific article published in April 2007

Idalopirdine as a treatment for Alzheimer's disease

scientific article published on 28 May 2015

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

scientific article

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

scientific article published in December 2015

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

scientific article

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

scientific article

Immunotherapy against amyloid pathology in Alzheimer's disease

scientific article

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

scientific article published on January 2017

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

scientific article published on 24 September 2007

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

scientific article

Increased PCSK9 Cerebrospinal Fluid Concentrations in Alzheimer's Disease

scientific article published on 20 September 2016

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

scientific article

Inflammation and oxidative damage in Alzheimer's disease: friend or foe?

scientific article

Inflammation in dry eye associated with rheumatoid arthritis: cytokine and in vivo confocal microscopy study

scientific article published on 22 January 2013

Inflammation in neurodegenerative disorders: friend or foe?

scientific article

Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola Disease

scientific article published on 25 January 2019

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

scientific article published on 27 May 2015

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

scientific article

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

scientific article

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

scientific article published on 26 April 2007

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

scientific article published on 18 April 2009

Intrathecal chemokine levels in Alzheimer disease and frontotemporal lobar degeneration.

scientific article

Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer disease

scientific article

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

scientific article

Investigation of c9orf72 in 4 neurodegenerative disorders

scientific article published on December 2012

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

scientific article published on 28 November 2015

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

scientific article

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

scientific article

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

scientific article

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

scientific article

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

scientific article published on 21 December 2014

Kappa free light chains is a valid tool in the diagnostics of MS: A large multicenter study

scientific article published on 08 May 2019

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

scientific article published on 7 April 2011

Lack of adiponectin leads to increased lymphocyte activation and increased disease severity in a mouse model of multiple sclerosis

scientific article published on 07 June 2013

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

scientific article

Lag-time in Alzheimer’s disease patients: a potential plasmatic oxidative stress marker associated with ApoE4 isoform

scientific article published on 01 April 2019

Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation

scientific article published on 07 September 2020

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

scientific article

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

scientific article

Low frequency and rare coding variation contributes to multiple sclerosis risk

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

scientific article

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

scientific article published in October 2004

MDC/CCL22 intrathecal levels in patients with multiple sclerosis.

scientific article

MRI helps depict clinically undetectable risk factors in advanced stage retinoblastomas

scientific article published on February 2015

Menopausal transition: a possible risk factor for brain pathologic events

scientific article published on 2 July 2007

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

scientific article published on 5 September 2017

MiRNA Profiling in Plasma Neural-Derived Small Extracellular Vesicles from Patients with Alzheimer's Disease

scientific article published on 10 June 2020

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

scientific article published on 07 November 2011

MicroRNAs as active players in the pathogenesis of multiple sclerosis

scientific article published on 15 October 2012

Microtubule defects in mesenchymal stromal cells distinguish patients with Progressive Supranuclear Palsy.

scientific article published on 4 March 2018

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

scientific article published on 01 January 2019

Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid

scientific article published on 03 March 2011

Mutation analysis of CHCHD10 in different neurodegenerative diseases

scientific article published on 31 March 2015

Neurofilament light chain and oligoclonal bands are prognostic biomarkers in radiologically isolated syndrome

scientific article published on 14 February 2018

Neurofilament light chain: a biomarker for genetic frontotemporal dementia

scientific article published on July 2016

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

scientific article published on 7 May 2016

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

scientific article published on 27 November 2007

Neuronal pentraxin 2: a synapse-derived CSF biomarker in genetic frontotemporal dementia

scientific article published on 09 April 2020

New insights into the genetic etiology of Alzheimer's disease and related dementias

scientific article published in April 2022

New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations

scholarly article published 23 July 2021

NfL reliability across laboratories, stage-dependent diagnostic performance and matrix comparability in genetic FTD: a large GENFI study

scholarly article published on 19 January 2024

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

scientific article

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

scientific article published on 10 August 2016

Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature

scientific article

Novel CSF biomarkers to discriminate FTLD and its pathological subtypes

scientific article published on 07 September 2018

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

scientific article published on January 2013

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

scientific article published on 26 August 2008

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

scientific article

Old and new acetylcholinesterase inhibitors for Alzheimer's disease

scientific article

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

scientific article published on 26 November 2011

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

scientific article published in January 2010

Overlap Between Frontotemporal Dementia and Dementia with Lewy Bodies: A Treviso Dementia (TREDEM) Registry Case Report

scientific article published on 01 January 2019

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

scientific article published on 17 February 2005

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

scientific article published on 01 November 2005

P2‐182: DEFECTIVE MIRNA‐223‐MEDIATED REGULATION OF NLRP3 INFLAMMASOME ACTIVATION IN ALZHEIMER'S DISEASE

scholarly article

P2‐183: ANALYSIS OF IL‐33 AND ITS DECOY RECEPTOR SST2 IN ALZHEIMER'S DISEASE AND MILD COGNITIVE IMPAIRMENT PATIENTS

scholarly article

PICALM Gene Methylation in Blood of Alzheimer's Disease Patients Is Associated with Cognitive Decline

scientific article published on 01 January 2018

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

scientific article published on 6 January 2016

Parieto-occipital sulcus widening differentiates posterior cortical atrophy from typical Alzheimer disease

scientific article published on 28 September 2020

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

scientific article published on January 2014

Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

scientific article published on 19 October 2017

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

scientific article published on 29 January 2013

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

scientific article published on January 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

scientific article published on January 2014

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

scientific article published in January 2014

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

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Pioglitazone for the treatment of Alzheimer's disease

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Plasma Protein Biomarkers for the Prediction of CSF Amyloid and Tau and [F]-Flutemetamol PET Scan Result

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

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Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia

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

scientific article published on 25 April 2006

Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers.

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

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

scientific article published in January 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

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

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

scientific article published on August 2008

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

scientific article published on 6 September 2006

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

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Presymptomatic white matter integrity loss in familial frontotemporal dementia in the GENFI cohort: A cross-sectional diffusion tensor imaging study

scientific article published on 11 July 2018

Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosis

scientific article published on 01 October 2005

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

scientific article published in January 2018

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

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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

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Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

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

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

scientific article published on 6 February 2014

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

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

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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

scientific article published on 14 August 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

scientific article published on 13 November 2017

Progress in Alzheimer's disease

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Progress in Alzheimer's disease research in the last year

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Progress in multiple sclerosis research in the last year

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Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia

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

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

scientific article published on 8 April 2015

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

scientific article published on 15 November 2016

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

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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

scientific article published on 16 February 2017

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

scientific article published on 04 March 2020

Regulation of gene transcription in bipolar disorders: Role of DNA methylation in the relationship between prodynorphin and brain derived neurotrophic factor.

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Repetitive element hypermethylation in multiple sclerosis patients.

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

scientific article published in January 2012

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

scientific article published on 19 January 2016

Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

scientific article published on 01 November 2019

Role of Genetics and Epigenetics in the Pathogenesis of Alzheimer's Disease and Frontotemporal Dementia.

scientific article published in January 2018

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

scientific article published in January 2011

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

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

scientific article published on 6 May 2011

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

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SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis

scientific article published on 27 October 2005

SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer's Disease

scientific article published on 01 January 2019

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

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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

scientific article published on 12 September 2012

Sciatic endometriosis presenting as periodic (catamenial) sciatic radiculopathy

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

scientific article published on 11 October 2012

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

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Self-Awareness for Memory Impairment in Amnestic Mild Cognitive Impairment: A Longitudinal Study

scientific article published in January 2017

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

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

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Serum folate concentrations in patients with cortical and subcortical dementias

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Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

scientific article published on 01 December 2019

Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort

scientific article published on 26 September 2020

Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort

Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: applied to GENFI study

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

scientific article published on 13 December 2018

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

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T cells producing GM-CSF and IL-13 are enriched in the cerebrospinal fluid of relapsing MS patients

scientific article published on 25 June 2019

TREM2 regulates microglial cell activation in response to demyelination in vivo

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

scientific article published on 15 October 2019

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

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

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

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The CST3 B haplotype is associated with frontotemporal lobar degeneration.

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The Cornea in Sjögren’s Syndrome: An In Vivo Confocal Study

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

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

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The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies design.

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The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

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

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The Neuroanatomy of Somatoform Disorders: A Magnetic Resonance Imaging Study

scientific article published on 20 July 2018

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

The Role of Amyloid-β in White Matter Damage: Possible Common Pathogenetic Mechanisms in Neurodegenerative and Demyelinating Diseases

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

scientific article published on 30 May 2012

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

scientific article published on 7 April 2005

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

scientific article published on 01 June 2008

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

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

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The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint

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

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

scientific article published in November 2017

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

scientific article published in January 2015

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

scientific article published on 18 July 2013

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

scientific article published in January 2009

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

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Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

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

scientific article published in January 2015

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

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Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

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Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

Untangling Extracellular Proteasome-Osteopontin Circuit Dynamics in Multiple Sclerosis

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

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

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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.

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Ventricular volume expansion in presymptomatic genetic frontotemporal dementia

scientific article published on 02 October 2019

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

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White Matter Hyperintensities are No Major Confounder for Alzheimer's Disease Cerebrospinal Fluid Biomarkers

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

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White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study

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

scientific article published on 8 October 2017