51 results on '"Daniela Galimberti"'
Search Results
2. Feasibility of implementing a standard cognitive assessment in Italian academic and non‐academic memory clinics
3. Protective association of HLA‐DRB1 *04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences
4. Apathy in presymptomatic genetic frontotemporal dementia predicts cognitive decline and is driven by structural brain changes
5. Differences in sex distribution between genetic and sporadic FTD
6. A data‐driven disease progression model of fluid biomarkers in genetic FTD
7. A cognitive composite for genetic frontotemporal dementia: GENFI‐cog
8. Dissecting frontotemporal dementia: Correlations between neuropsychiatric symptoms and neuropathology
9. Phenotypic heterogeneity of the rare R377W PSEN1 mutation: Late‐onset presentation with mixed Alzheimer’s and frontotemporal dementia features
10. Subtype and stage inference identifies distinct atrophy patterns in genetic frontotemporal dementia that MAP onto specific MAPT mutations
11. The Free Cued Selective Reminding Test detects episodic memory impairment in the presymptomatic period of familial frontotemporal dementia within the GENFI cohort
12. Trajectory of apathy, cognition and neural correlates in the decades before symptoms in frontotemporal dementia
13. P2‐179: STAVUDINE INHIBITS INFLAMMASOME ACTIVATION MOLECULAR INHIBITOR IN PERIPHERAL‐MONOCYTES OF AD PATIENTS
14. P1-380: EARLY REGIONAL HYPOMETABOLISM IN PRE-SYMPTOMATIC CARRIERS OF MAPT : A GENFI SUB-STUDY
15. [IC‐P‐079]: MULTIPLE DISTINCT ATROPHY PATTERNS FOUND IN GENETIC FRONTOTEMPORAL DEMENTIA USING SUBTYPE AND STAGE INFERENCE (SUSTAIN)
16. [IC‐03–04]: WHITE MATTER HYPERINTENSITIES IN GENETIC FRONTOTEMPORAL DEMENTIA: A GENFI STUDY
17. [P1–029]: IN GENETIC FRONTOTEMPORAL DEMENTIA, FUNCTIONAL NETWORK EFFICIENCY IS MAINTAINED UNTIL THE ONSET OF SYMPTOMS: EVIDENCE FOR FUNCTIONAL RESILIENCE TO STRUCTURAL CHANGE
18. [P4–189]: SYMPTOM ONSET IN GENETIC FRONTOTEMPORAL DEMENTIA
19. [P1–437]: PRESYMPTOMATIC WHITE MATTER INTEGRITY LOSS IN FAMILIAL FRONTOTEMPORAL DEMENTIA IN THE GENETIC FRONTOTEMPORAL DEMENTIA INITIATIVE (GENFI) COHORT: A MULTI‐CENTRE, CROSS‐SECTIONAL, DIFFUSION TENSOR IMAGING STUDY
20. P2-183: ANALYSIS OF IL-33 AND ITS DECOY RECEPTOR SST2 IN ALZHEIMER'S DISEASE AND MILD COGNITIVE IMPAIRMENT PATIENTS
21. P2-182: DEFECTIVE MIRNA-223-MEDIATED REGULATION OF NLRP3 INFLAMMASOME ACTIVATION IN ALZHEIMER'S DISEASE
22. O4-03-06: LONGITUDINAL ASSOCIATION BETWEEN APATHY AND COGNITIVE DECLINE IN PRE- AND POST-SYMPTOMATIC GENETIC FRONTOTEMPORAL DEMENTIA
23. S4‐01‐01: Cross‐Sectional Studies of Plasma Proteomic Biomarkers Relating to Pet Amyloid and CSF Amyloid and Tau
24. O5‐05‐03: Novel CSF Biomarkers Discriminating FTLD‐TDP from Non‐Demented Controls
25. P1‐025: Cerebral Perfusion as an Imaging Biomarker of Presymptomatic Genetic Frontotemporal Dementia: Preliminary Results from the Genetic Frontotemporal Dementia Initiative (GENFI)
26. IC‐P‐054: Grey matter differences in genetic frontotemporal dementia: Results from the genfi study
27. F2‐03‐04: Genetic risk factors for posterior cortical atrophy
28. O2‐01‐01: Grey matter differences in genetic frontotemporal dementia: Results from the genfi study
29. P4‐009: Frontotemporal dementia and parkinsonism linked to chromosome 17 granulin: Clinical and pathologic study of a patient from a new pedigree
30. P1‐115: Consensus guidelines to perform lumbar puncture for CSF sampling in patients with neurological conditions
31. P1‐044: TREM2 GENETIC VARIABILITY IN PATIENTS WITH ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION
32. P1‐043: CIRCULATING AND INTRATHECAL MIRNAS AS POTENTIAL BIOMARKERS FOR ALZHEIMER'S DISEASE
33. P4‐074: ITALIAN NETWORK FOR AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION (ITALIANDIAFN)
34. IC‐P‐069: ITALIAN NETWORK FOR AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION (ITALIANDIAFN)
35. P3‐104: A NOVEL MUTATION IN PROGRANULIN GENE IN BEHAVIOURAL VARIANT FRONTO‐TEMPORAL DEMENTIA
36. P1‐231: Role of OLR1 and Its Regulating hsa‐miR369‐3p in Alzheimer's Disease: Genetic and Expression Analysis
37. P1‐282: Annamaria Confaloni PhD
38. P1‐286: A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
39. P1‐092: Chromosome 9 and sporadic Frontotemporal Lobar Degeneration: KIF24, but not UBAP1, is a risk factor in Italian population
40. P4‐101: Urea cycle and Alzheimer's disease
41. P4‐107: Association study of the ADAM12 and SH3MD1 genes with the risk of developing Alzheimer's disease
42. O2‐06–06: SNPS in MAPT are associated with cerebrospinal fluid Tau levels, MAPT mRNA levels, and age at onset of late‐onset Alzheimer's disease
43. P1‐207: APOE alleles distribution in different forms of mild cognitive impairment
44. P1–444: Low doses of memantine are effective in reducing behavioral symptoms in AD patients
45. P1–177: Total folate levels in Alzheimer disease and other forms of degenerative cognitive decline
46. P1–221: Association between dementia and cancer
47. P3–167: Absence of mutations in TREM–2 coding region in early onset dementia
48. P1–329: Presenilin–1 mutation E318G in Italian population: Genetic screening and effect on beta amyloid metabolism in human fibroblasts
49. P2–138: Chemokine serum levels in mild cognitive impairment as Alzheimer's disease early biomarkers
50. P3-217: Genetic and functional analysis of progranulin gene variants in patients with Alzheimer's disease
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