Pages that link to "Q64856448"
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The following pages link to Giuliano Binetti (Q64856448):
Displaying 50 items.
- Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease (Q21136190) (← links)
- A window into the heterogeneity of human cerebrospinal fluid Aβ peptides (Q27010785) (← links)
- CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration (Q28243714) (← links)
- Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease (Q28285955) (← links)
- Detection of the presenilin 1 COOH-terminal fragment in the extracellular compartment: a release enhanced by apoptosis (Q28572591) (← links)
- A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia (Q30402493) (← links)
- Cystatin C is released in association with exosomes: a new tool of neuronal communication which is unbalanced in Alzheimer's disease. (Q33505900) (← links)
- GRN variability contributes to sporadic frontotemporal lobar degeneration (Q33522914) (← links)
- Behavioral and neurophysiological effects of transdermal rotigotine in atypical parkinsonism. (Q33713621) (← links)
- Rotigotine is safe and efficacious in Atypical Parkinsonism Syndromes induced by both α-synucleinopathy and tauopathy. (Q33734770) (← links)
- Optimization protocol for amyloid-β peptides detection in human cerebrospinal fluid using SELDI TOF MS. (Q33778885) (← links)
- Comparison of the effects of transdermal and oral rivastigmine on cognitive function and EEG markers in patients with Alzheimer's disease (Q33937187) (← links)
- Frontotemporal dementia and its subtypes: a genome-wide association study (Q33955007) (← links)
- Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration (Q34038343) (← links)
- Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients (Q34121245) (← links)
- High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes (Q34146052) (← links)
- H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers. (Q34325847) (← links)
- Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementia. (Q34467344) (← links)
- TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers. (Q34555400) (← links)
- No association between DCP1 genotype and late-onset Alzheimer disease. (Q34626057) (← links)
- Value of serum nonceruloplasmin copper for prediction of mild cognitive impairment conversion to Alzheimer disease. (Q34660301) (← links)
- Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer's disease (Q34996283) (← links)
- Temporal lobe asymmetry in patients with Alzheimer's disease with delusions (Q35458508) (← links)
- Specific EEG changes associated with atrophy of hippocampus in subjects with mild cognitive impairment and Alzheimer's disease. (Q35810855) (← links)
- Medial temporal atrophy but not memory deficit predicts progression to dementia in patients with mild cognitive impairment. (Q36141850) (← links)
- A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia (Q36444721) (← links)
- Analysis of grey matter in thalamus and basal ganglia based on EEG α3/α2 frequency ratio reveals specific changes in subjects with mild cognitive impairment (Q36466486) (← links)
- A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease (Q37099304) (← links)
- TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia (Q37154601) (← links)
- C9ORF72 repeat expansions in cases with previously identified pathogenic mutations (Q37251674) (← links)
- EEG upper/low alpha frequency power ratio relates to temporo-parietal brain atrophy and memory performances in mild cognitive impairment. (Q37253788) (← links)
- Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort (Q37325871) (← links)
- Mapping the effect of APOE epsilon4 on gray matter loss in Alzheimer's disease in vivo (Q37337930) (← links)
- Increase of theta frequency is associated with reduction in regional cerebral blood flow only in subjects with mild cognitive impairment with higher upper alpha/low alpha EEG frequency power ratio. (Q37365365) (← links)
- TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis (Q37664119) (← links)
- Anatomical Substrate and Scalp EEG Markers are Correlated in Subjects with Cognitive Impairment and Alzheimer's Disease (Q37855550) (← links)
- Cerebrospinal fluid biomarkers for Alzheimer's disease: the present and the future. (Q37895052) (← links)
- Losing protein in the brain: the case of progranulin. (Q37986220) (← links)
- Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration? (Q38371631) (← links)
- Action and object naming in frontotemporal dementia, progressive supranuclear palsy, and corticobasal degeneration. (Q38404304) (← links)
- Semantic memory in Alzheimer's disease: an analysis of category fluency. (Q38464327) (← links)
- Progranulin Mutations Affects Brain Oscillatory Activity in Fronto-Temporal Dementia. (Q38667291) (← links)
- Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia. (Q38765067) (← links)
- Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. (Q39041947) (← links)
- Preliminary evidence of validity of the revised criteria for Alzheimer disease diagnosis: report of 2 cases. (Q39966471) (← links)
- Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. (Q40051471) (← links)
- Blockade of the tumor necrosis factor-related apoptosis inducing ligand death receptor DR5 prevents beta-amyloid neurotoxicity. (Q40238974) (← links)
- Apolipoprotein E and alpha brain rhythms in mild cognitive impairment: a multicentric electroencephalogram study. (Q40364742) (← links)
- Genotype (cystatin C) and EEG phenotype in Alzheimer disease and mild cognitive impairment: a multicentric study (Q40382607) (← links)
- Interaction between tau and alpha-synuclein proteins is impaired in the presence of P301L tau mutation. (Q40420217) (← links)