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Your search keyword '"Rossi, Giacomina"' showing total 27 results

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27 results on '"Rossi, Giacomina"'

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

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

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

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

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

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

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

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

11. 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]

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

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

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

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

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

27. A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations

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