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69 results on '"Ghidoni, Roberta"'

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1. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

2. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

3. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

4. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

5. Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia

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

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

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

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

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

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

13. Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

14. Loss of exosomes in progranulin-associated frontotemporal dementia

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

17. The SIRT2 polymorphism rs10410544 and risk of Alzheimer’s disease in two Caucasian case–control cohorts

19. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

20. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

21. Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

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

29. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

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

39. Presenilin 1 Protein Directly Interacts with Bcl-2

40. POLY-GP DIPEPTIDE REPEATS AND NEUROFILAMENT LIGHT CHAIN AS BIOMARKERS IN PRESYMPTOMATIC AND SYMPTOMATIC FRONTOTEMPORAL DEMENTIA CAUSED BY C9ORF72 REPEAT EXPANSIONS

42. ITALIAN NETWORK FOR AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION (ITALIANDIAFN)

43. ITALIAN NETWORK FOR AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION (ITALIANDIAFN)

50. Chromosome 9 and sporadic Frontotemporal Lobar Degeneration: KIF24, but not UBAP1, is a risk factor in Italian population

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