Daniela Galimberti

Neurology Unit, University of Milan

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2016

Other Publications

Article	Year
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration. Neuroscience letters\| PubMed ID: 17088018	2007
Association of a NOS1 promoter repeat with Alzheimer's disease. Neurobiology of aging\| PubMed ID: 17418914	2008
The cornea in Sjogren's syndrome: an in vivo confocal study. Investigative ophthalmology & visual science\| PubMed ID: 17460255	2007
Interaction between the APOE epsilon4 allele and the APH-1b c + 651T > G SNP in Alzheimer's disease. Neurobiology of aging\| PubMed ID: 17466415	2008
ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution. Journal of neuroimmunology\| PubMed ID: 17481737	2007
Serum folate concentrations in patients with cortical and subcortical dementias. Neuroscience letters\| PubMed ID: 17532571	2007
Role of VEGF gene variability in longevity: a lesson from the Italian population. Neurobiology of aging\| PubMed ID: 17574707	2008
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis. Neuroscience letters\| PubMed ID: 17825989	2007
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation. Neurobiology of aging\| PubMed ID: 17889967	2009
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis. Journal of the neurological sciences\| PubMed ID: 17967467	2008
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration. Journal of neurology\| PubMed ID: 18204920	2008
Corneal involvement in rheumatoid arthritis: an in vivo confocal study. Investigative ophthalmology & visual science\| PubMed ID: 18234999	2008
Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series. Neurogenetics\| PubMed ID: 18392865	2008
Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 18541914	2008
A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk. Cell\| PubMed ID: 18585350	2008
Polymorphisms in the LOC387715/ARMS2 putative gene and the risk for Alzheimer's disease. Dementia and geriatric cognitive disorders\| PubMed ID: 18688167	2008
Identification of soluble TREM-2 in the cerebrospinal fluid and its association with multiple sclerosis and CNS inflammation. Brain : a journal of neurology\| PubMed ID: 18790823	2008
Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease? Neuroscience letters\| PubMed ID: 18983895	2009
Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy. Journal of human genetics\| PubMed ID: 19020798	2008
Candidate gene analysis of selectin cluster in patients with multiple sclerosis. Journal of neurology\| PubMed ID: 19240957	2009
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. Age (Dordrecht, Netherlands)\| PubMed ID: 19377912	2009
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration. Journal of neurology\| PubMed ID: 19415413	2009
Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of aging\| PubMed ID: 19427062	2011
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels. Journal of Alzheimer's disease : JAD\| PubMed ID: 19494437	2009
Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy. European neurology\| PubMed ID: 19521089	2009
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 19625741	2009
The serotonin transporter promoter polymorphic region is not a risk factor for Alzheimer's disease related behavioral disturbances. Journal of Alzheimer's disease : JAD\| PubMed ID: 19625753	2009
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiology of aging\| PubMed ID: 19632744	2011
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 Alzhe... Journal of the neurological sciences\| PubMed ID: 19683260	2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nature genetics\| PubMed ID: 19734903	2009
Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration. Dementia and geriatric cognitive disorders\| PubMed ID: 19786775	2009
Alpha1-antichymotrypsin induces TNF-alpha production and NF-kappaB activation in the murine N9 microglial cell line. Neuroscience letters\| PubMed ID: 19800391	2009
Analysis of the genes coding for subunit 10 and 15 of cytochrome c oxidase in Alzheimer's disease. Journal of neural transmission (Vienna, Austria : 1996)\| PubMed ID: 19826901	2009
A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience letters\| PubMed ID: 19837132	2010
Candidate gene analysis of semaphorins in patients with Alzheimer's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology\| PubMed ID: 19957197	2010
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes. Neuroscience letters\| PubMed ID: 19963041	2010
Inflammation in neurodegenerative disorders: friend or foe? Current aging science\| PubMed ID: 20021370	2008
FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration. Journal of Alzheimer's disease : JAD\| PubMed ID: 20061612	2010
GRN variability contributes to sporadic frontotemporal lobar degeneration. Journal of Alzheimer's disease : JAD\| PubMed ID: 20061636	2010
The H1 haplotype of the tau gene (MAPT) is associated with mild cognitive impairment. Journal of Alzheimer's disease : JAD\| PubMed ID: 20157246	2010
Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population. PloS one\| PubMed ID: 20174631	2010
Treatment of Alzheimer's disease: symptomatic and disease-modifying approaches. Current aging science\| PubMed ID: 20298170	2010
Osteopontin is increased in the cerebrospinal fluid of patients with Alzheimer's disease and its levels correlate with cognitive decline. Journal of Alzheimer's disease : JAD\| PubMed ID: 20308780	2010
In vivo confocal microscopy of the ocular surface. American journal of ophthalmology\| PubMed ID: 20346790	2010
Loss of epidermal growth factor regulation by cobalamin in multiple sclerosis. Brain research\| PubMed ID: 20347721	2010
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients. Journal of Alzheimer's disease : JAD\| PubMed ID: 20555150	2010
Genetics and biology of Alzheimer's disease and frontotemporal lobar degeneration. International journal of clinical and experimental medicine\| PubMed ID: 20607039	2010
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration? Neuroscience letters\| PubMed ID: 20670673	2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's disease : JAD\| PubMed ID: 20847397	2010
Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration. Neurobiology of aging\| PubMed ID: 20947212	2011
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population. Journal of medical genetics\| PubMed ID: 21037273	2011
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease. Journal of neurology\| PubMed ID: 21069533	2011
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 21157029	2011
In vivo confocal microscopy of meibomian glands in Sjögren's syndrome. Investigative ophthalmology & visual science\| PubMed ID: 21169534	2011
Inflammation and oxidative damage in Alzheimer's disease: friend or foe? Frontiers in bioscience (Scholar edition)\| PubMed ID: 21196374	2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Neurobiology of aging\| PubMed ID: 21220176	2011
Alzheimer's disease: from pathogenesis to disease-modifying approaches. CNS & neurological disorders drug targets\| PubMed ID: 21222635	2011
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred. Journal of Alzheimer's disease : JAD\| PubMed ID: 21258152	2011
An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 21263195	2011
Multiple sclerosis: BAFF and CXCL13 in cerebrospinal fluid. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 21372118	2011
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. Journal of medical genetics\| PubMed ID: 21441263	2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature genetics\| PubMed ID: 21460840	2011
Genetic variation in the choline O-acetyltransferase gene in depression and Alzheimer's disease: the VITA and Milano studies. Journal of psychiatric research\| PubMed ID: 21507424	2011
In vivo confocal microscopy of conjunctival roundish bright objects: young, older, and Sjögren subjects. Investigative ophthalmology & visual science\| PubMed ID: 21508113	2011
GSK3β genetic variability in patients with Multiple Sclerosis. Neuroscience letters\| PubMed ID: 21527318	2011
APOE ε2 and ε4 influence the susceptibility for Alzheimer's disease but not other dementias. International journal of molecular epidemiology and genetics\| PubMed ID: 21537391	2010
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration. Rejuvenation research\| PubMed ID: 21548758	2011
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia. Journal of Alzheimer's disease : JAD\| PubMed ID: 21558644	2011
Lack of Association between the GPR3 Gene and the Risk for Alzheimer's Disease. International journal of Alzheimer's disease\| PubMed ID: 21559181	2011
Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patients. Journal of neuroinflammation\| PubMed ID: 21645364	2011
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. International journal of Alzheimer's disease\| PubMed ID: 21660253	2011
Progress in Alzheimer's disease. Journal of neurology\| PubMed ID: 21706152	2012
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis. Journal of Alzheimer's disease : JAD\| PubMed ID: 21709374	2011
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis. Human genetics\| PubMed ID: 21735172	2012
Disease-modifying treatments for Alzheimer's disease. Therapeutic advances in neurological disorders\| PubMed ID: 21765871	2011
The Alzheimer's Association external quality control program for cerebrospinal fluid biomarkers. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 21784349	2011
Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene. Biological psychiatry\| PubMed ID: 21791336	2011
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature\| PubMed ID: 21833088	2011
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis. Neuroscience letters\| PubMed ID: 21875645	2011
Cerebrospinal fluid biomarkers in Progranulin mutations carriers. Journal of Alzheimer's disease : JAD\| PubMed ID: 21891865	2011
From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder. Journal of Alzheimer's disease : JAD\| PubMed ID: 21891869	2011
The progranulin (GRN) Cys157LysfsX97 mutation is associated with nonfluent variant of primary progressive aphasia clinical phenotype. Journal of Alzheimer's disease : JAD\| PubMed ID: 22072213	2012
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers. Neuroscience letters\| PubMed ID: 22108567	2012
Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study. Neuro-degenerative diseases\| PubMed ID: 22123177	2012
Sciatic endometriosis presenting as periodic (catamenial) sciatic radiculopathy. Journal of neurology\| PubMed ID: 22215240	2012
A functional variant in ERAP1 predisposes to multiple sclerosis. PloS one\| PubMed ID: 22253828	2012
Behavioral genetics of neurodegenerative disorders. Current topics in behavioral neurosciences\| PubMed ID: 22261700	2012
Possible influence of a non-synonymous polymorphism located in the NGF precursor on susceptibility to late-onset Alzheimer's disease and mild cognitive impairment. Journal of Alzheimer's disease : JAD\| PubMed ID: 22330829	2012
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology\| PubMed ID: 22353757	2012
Clinical, neuropathological, and genetic characteristics of the novel IVS9+1delG GRN mutation in a patient with frontotemporal dementia. Journal of Alzheimer's disease : JAD\| PubMed ID: 22366770	2012
Replication study to confirm the role of CYP2D6 polymorphism rs1080985 on donepezil efficacy in Alzheimer's disease patients. Journal of Alzheimer's disease : JAD\| PubMed ID: 22465999	2012
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia. PloS one\| PubMed ID: 22505994	2012
Clinical phenotypes and genetic biomarkers of FTLD. Journal of neural transmission (Vienna, Austria : 1996)\| PubMed ID: 22527778	2012
Frontotemporal lobar degeneration: current knowledge and future challenges. Journal of neurology\| PubMed ID: 22532172	2012
Genetics of frontotemporal lobar degeneration. Frontiers in neurology\| PubMed ID: 22536193	2012
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations. Journal of Alzheimer's disease : JAD\| PubMed ID: 22571983	2012
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration. Journal of Alzheimer's disease : JAD\| PubMed ID: 22614877	2012
The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 22651940	2013
Epigenetic regulation of fatty acid amide hydrolase in Alzheimer disease. PloS one\| PubMed ID: 22720070	2012
Progress in multiple sclerosis research in the last year. Journal of neurology\| PubMed ID: 22722387	2012
Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology\| PubMed ID: 22797721	2013
Epigenetic modulation of BDNF gene in patients with major depressive disorder. Biological psychiatry\| PubMed ID: 22901293	2013
Investigation of C9orf72 in 4 Neurodegenerative Disorders. Archives of neurology\| PubMed ID: 22964832	2012
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Neurology\| PubMed ID: 22972638	2012
The impact of osteopontin gene variations on multiple sclerosis development and progression. Clinical & developmental immunology\| PubMed ID: 23008732	2012
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. Neurobiology of aging\| PubMed ID: 23063648	2013
Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. Neuroscience letters\| PubMed ID: 23069673	2012
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. Neurology\| PubMed ID: 23115207	2012
Does vascular burden contribute to the progression of mild cognitive impairment to dementia? Dementia and geriatric cognitive disorders\| PubMed ID: 23147614	2012
MicroRNAs as active players in the pathogenesis of multiple sclerosis. International journal of molecular sciences\| PubMed ID: 23202949	2012
Immunotherapy against amyloid pathology in Alzheimer's disease. Journal of the neurological sciences\| PubMed ID: 23299047	2013
Inflammation in dry eye associated with rheumatoid arthritis: cytokine and in vivo confocal microscopy study. Innate immunity\| PubMed ID: 23339928	2013
Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors. Neurobiology of aging\| PubMed ID: 23374588	2013
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD. Antioxidants & redox signaling\| PubMed ID: 23379482	2013
Gender effects on plasma PGRN levels in patients with Alzheimer's disease: a preliminary study. Journal of Alzheimer's disease : JAD\| PubMed ID: 23396349	2013
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 23435408	2013
Novel evidence of phenotypical variability in the hexanucleotide repeat expansion in chromosome 9. Journal of Alzheimer's disease : JAD\| PubMed ID: 23435409	2013
Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis. International journal of molecular sciences\| PubMed ID: 23439547	2013
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation. Biological psychiatry\| PubMed ID: 23473366	2013
GRN Thr272fs clinical heterogeneity: a case with atypical late onset presenting with a dementia with Lewy bodies phenotype. Journal of Alzheimer's disease : JAD\| PubMed ID: 23478307	2013
Progress in Alzheimer's disease research in the last year. Journal of neurology\| PubMed ID: 23595792	2013
Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia. Journal of Alzheimer's disease : JAD\| PubMed ID: 23624518	2013
Lack of adiponectin leads to increased lymphocyte activation and increased disease severity in a mouse model of multiple sclerosis. European journal of immunology\| PubMed ID: 23640763	2013
Consensus definitions and application guidelines for control groups in cerebrospinal fluid biomarker studies in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 23695446	2013
Estimating the inheritance of frontotemporal lobar degeneration in the Italian population. Journal of Alzheimer's disease : JAD\| PubMed ID: 23719513	2014
Intra-arterial chemotherapy with melphalan for intraocular retinoblastoma. The British journal of ophthalmology\| PubMed ID: 23853166	2013
The role of the innate immune system in Alzheimer's disease and frontotemporal lobar degeneration: an eye on microglia. Clinical & developmental immunology\| PubMed ID: 23970926	2013
Dementia: not only Alzheimer's disease, an eye on frontotemporal dementia. Acta médica portuguesa\| PubMed ID: 24016634	2013
Evidence of pre-synaptic dopaminergic deficit in a patient with a novel progranulin mutation presenting with atypical parkinsonism. Journal of Alzheimer's disease : JAD\| PubMed ID: 24064467	2014
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature genetics\| PubMed ID: 24076602	2013
Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects. Journal of Alzheimer's disease : JAD\| PubMed ID: 24121957	2014
An emerging role for long non-coding RNA dysregulation in neurological disorders. International journal of molecular sciences\| PubMed ID: 24129177	2013
Heterozygous TREM2 mutations in frontotemporal dementia. Neurobiology of aging\| PubMed ID: 24139279	2014
Brain temperature in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 24158976	2014
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 24277735	2013
Physical activity reduces the risk of dementia in mild cognitive impairment subjects: a cohort study. Journal of Alzheimer's disease : JAD\| PubMed ID: 24296815	2014
Successful treatment of macular retinoblastoma with superselective ophthalmic artery infusion of melphalan. Journal of pediatric ophthalmology and strabismus\| PubMed ID: 24308859	2014
C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder. Bipolar disorders\| PubMed ID: 24329881	2014
Partial recovery after severe immune reconstitution inflammatory syndrome in a multiple sclerosis patient with progressive multifocal leukoencephalopathy. Immunotherapy\| PubMed ID: 24341880	2014
Disease-modifying drugs in Alzheimer's disease. Drug design, development and therapy\| PubMed ID: 24353405	2013
C9ORF72 repeat expansion not detected in patients with multiple sclerosis. Neurobiology of aging\| PubMed ID: 24355526	2014
C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia. Neurobiology of aging\| PubMed ID: 24387986	2014
Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder. Bipolar disorders\| PubMed ID: 24499389	2014
Familial clustering in Italian progressive-onset and bout-onset multiple sclerosis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology\| PubMed ID: 24514917	2014
Current understanding on the role of standard and immunoproteasomes in inflammatory/immunological pathways of multiple sclerosis. Autoimmune diseases\| PubMed ID: 24523959	2014
Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic defi... Journal of Alzheimer's disease : JAD\| PubMed ID: 24531155	2014
Innate immune system and inflammation in Alzheimer's disease: from pathogenesis to treatment. Neuroimmunomodulation\| PubMed ID: 24557039	2014
No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis. Journal of neuroimmunology\| PubMed ID: 24794504	2014
Clinical and MRI correlates of disease progression in a case of nonfluent/agrammatic variant of primary progressive aphasia due to progranulin (GRN) Cys157LysfsX97 mutation. Journal of the neurological sciences\| PubMed ID: 24814951	2014
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients. Human molecular genetics\| PubMed ID: 24908669	2014
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. PloS one\| PubMed ID: 24922517	2014
Frontotemporal dementia and its subtypes: a genome-wide association study. The Lancet. Neurology\| PubMed ID: 24943344	2014
Is HCRTR2 a genetic risk factor for Alzheimer's disease? Dementia and geriatric cognitive disorders\| PubMed ID: 24969517	2014
Epigenetic modulation of BDNF gene: differences in DNA methylation between unipolar and bipolar patients. Journal of affective disorders\| PubMed ID: 25012449	2014
Possible association between SNAP-25 single nucleotide polymorphisms and alterations of categorical fluency and functional MRI parameters in Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 25024311	2014
Circulating miRNAs as potential biomarkers in Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 25024331	2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. Neurobiology of aging\| PubMed ID: 25085782	2014
Transmembrane protein 106B gene (TMEM106B) variability and influence on progranulin plasma levels in patients with Alzheimer's disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 25114081	2015
Guidelines for uniform reporting of body fluid biomarker studies in neurologic disorders. Neurology\| PubMed ID: 25150289	2014
Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients. Neurobiology of aging\| PubMed ID: 25158920	2014
The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia. Journal of Alzheimer's disease : JAD\| PubMed ID: 25261445	2015
Csf p-tau181/tau ratio as biomarker for TDP pathology in frontotemporal dementia. Amyotrophic lateral sclerosis & frontotemporal degeneration\| PubMed ID: 25352065	2015
CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis. Brain : a journal of neurology\| PubMed ID: 25576308	2015
Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutations. International journal of molecular sciences\| PubMed ID: 25580532	2015
TREM2 regulates microglial cell activation in response to demyelination in vivo. Acta neuropathologica\| PubMed ID: 25631124	2015
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. The Lancet. Neurology\| PubMed ID: 25662776	2015
Chitinase 3-like 1: prognostic biomarker in clinically isolated syndromes. Brain : a journal of neurology\| PubMed ID: 25688078	2015
Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism. European journal of human genetics : EJHG\| PubMed ID: 25712084	2015
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients. Acta neuropathologica\| PubMed ID: 25716178	2015
Mutation analysis of CHCHD10 in different neurodegenerative diseases. Brain : a journal of neurology\| PubMed ID: 25833818	2015
SORL1 Gene is Associated with the Conversion from Mild Cognitive Impairment to Alzheimer's Disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 25881907	2015
MRI helps depict clinically undetectable risk factors in advanced stage retinoblastomas. The neuroradiology journal\| PubMed ID: 25924174	2015
Psychiatric symptoms in frontotemporal dementia: epidemiology, phenotypes, and differential diagnosis. Biological psychiatry\| PubMed ID: 25958088	2015
Idalopirdine as a treatment for Alzheimer's disease. Expert opinion on investigational drugs\| PubMed ID: 26022777	2015
Balò's concentric sclerosis: still to be considered as a variant of multiple sclerosis? Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology\| PubMed ID: 26109007	2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. Neurobiology of aging\| PubMed ID: 26154020	2015
Progranulin genetic polymorphisms influence progression of disability and relapse recovery in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England)\| PubMed ID: 26447062	2016
Usefulness of Multi-Parametric MRI for the Investigation of Posterior Cortical Atrophy. PloS one\| PubMed ID: 26480294	2015
Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway? Neuro-degenerative diseases\| PubMed ID: 26613252	2016
Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay. Molecular neurodegeneration\| PubMed ID: 26627638	2015
Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status. Acta neuropathologica\| PubMed ID: 26754641	2016
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population. Journal of Alzheimer's disease : JAD\| PubMed ID: 26757195	2015
Emerging amyloid disease-modifying drugs for Alzheimer's disease. Expert opinion on emerging drugs\| PubMed ID: 26817686	2016
Reversible Mild Cognitive Impairment: The Role of Comorbidities at Baseline Evaluation. Journal of Alzheimer's disease : JAD\| PubMed ID: 26836169	2016
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol. Journal of Alzheimer's disease : JAD\| PubMed ID: 26901402	2016
Erratum to: Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay. Molecular neurodegeneration\| PubMed ID: 26907468	2016
Gene promoter methylation and expression of Pin1 differ between patients with frontotemporal dementia and Alzheimer's disease. Journal of the neurological sciences\| PubMed ID: 26944164	2016
Weight Loss Predicts Progression of Mild Cognitive Impairment to Alzheimer's Disease. PloS one\| PubMed ID: 26990757	2016
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 26993346	2016
Body Mass Index Predicts Progression of Mild Cognitive Impairment to Dementia. Dementia and geriatric cognitive disorders\| PubMed ID: 27028129	2016
Transcranial Direct Current Stimulation Modulates Cortical Neuronal Activity in Alzheimer's Disease. Frontiers in neuroscience\| PubMed ID: 27065792	2016
CHRNA7 Gene and Response to Cholinesterase Inhibitors in an Italian Cohort of Alzheimer's Disease Patients. Journal of Alzheimer's disease : JAD\| PubMed ID: 27104904	2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations. Journal of Alzheimer's disease : JAD\| PubMed ID: 27163810	2016
Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes. Journal of Alzheimer's disease : JAD\| PubMed ID: 27163816	2016
Old and new acetylcholinesterase inhibitors for Alzheimer's disease. Expert opinion on investigational drugs\| PubMed ID: 27459153	2016
Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation. Journal of Alzheimer's disease : JAD\| PubMed ID: 27567822	2016
Neurofilament light chain: a biomarker for genetic frontotemporal dementia. Annals of clinical and translational neurology\| PubMed ID: 27606344	2016
Growth Arrest Specific 6 Concentration is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's Disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 27636849	2016
Increased PCSK9 Cerebrospinal Fluid Concentrations in Alzheimer's Disease. Journal of Alzheimer's disease : JAD\| PubMed ID: 27662294	2016
Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels in patients with multiple sclerosis. Journal of neuroimmunology\| PubMed ID: 27725128	2016