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30 results on '"Rossi, Giacomina"'

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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. Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study

4. Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia

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

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

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

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

13. A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)

14. Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features

15. Corrigendum to “Dissemination in time and space in presymptomatic granulin mutation carriers: A spatial chronnectome study” [Neurobiology of Aging Volume 108, December 2021, Pages 155–167]

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

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

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

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