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Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's diseaseMeta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's diseaseA family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxiaAssociation of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disordersRole of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the diseaseDifferent implication of NEDD9 genetic variant in early and late-onset Alzheimer's diseaseCommon variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseaseGenome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseGenetics of vascular dementia - review from the ICVD working group.The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Sexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta-analysis.Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population.Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane.Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.A pilot study evaluating the contribution of SLC19A1 (RFC-1) 80G>a polymorphism to Alzheimer's disease in Italian Caucasians.Frontotemporal dementia and its subtypes: a genome-wide association study.Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationFailure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients.Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations.Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Mutation analysis of patients with neurodegenerative disorders using NeuroX arrayMeta-analysis of the association between variants in SORL1 and Alzheimer disease.Isolation of two cDNA clones from tomato containing two different superoxide dismutase sequences.Brain metabolic decreases related to the dose of the ApoE e4 allele in Alzheimer's diseaseMonomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons.Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits.A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaA pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease.Suitability of neuropsychological tests in patients with vascular dementia (VaD).Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects.Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications.Semantic dementia associated with mutation V363I in the tau gene.Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.Heterozygous TREM2 mutations in frontotemporal dementia.Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.The Methylenetetrahydrofolate Reductase C677T Polymorphism and Risk for Late-Onset Alzheimer's disease: Further Evidence in an Italian Multicenter Study.
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