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Your search keyword '"Rossi, Giacomina"' showing total 39 results

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39 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. Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort

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

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

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

6. Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort

9. Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort

10. Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

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

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

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

14. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

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

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

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

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

21. Frontotemporal dementia and its subtypes: a genome-wide association study

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

23. 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]

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

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

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

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