32 results on '"Geracitano, Silvana"'
Search Results
2. A new approach to broaden the range of eye colour identifiable by IrisPlex in DNA phenotyping
3. Occupation, Literacy, Anthropometric Traits, and Life Expectancy of Italian Men Born 1900–1910: Evidence From Military Conscription Registers
4. An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review
5. A Blood-Based Molecular Clock for Biological Age Estimation
6. Clinical and Prognostic Implications of Estimating Glomerular Filtration Rate by Three Different Creatinine-Based Equations in Older Nursing Home Residents
7. A Blood-Based Molecular Clock for Biological Age Estimation.
8. Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia
9. Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia
10. Clinical Manifestations of Highly Prevalent Corticosteroid-Binding Globulin Mutations in a Village in Southern Italy
11. A New Robust Epigenetic Model for Forensic Age Prediction
12. Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease
13. Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy
14. Inter-Individual Variability in Xenobiotic-Metabolizing Enzymes: Implications for Human Aging and Longevity
15. Cardiovascular risk profiling of long‐lived people shows peculiar associations with mortality compared with younger individuals
16. Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia
17. Uncoupling protein 4 (UCP4) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia
18. Cardiovascular risk profiling of long‐lived people shows peculiar associations with mortality compared with younger individuals.
19. The Impact of the Emerging Genomics Data on the Management of Agerelated Phenotypes in the Context of Cellular Senescence
20. A Novel Pathogenic PSEN1 Mutation in a Family with Alzheimer's Disease: Phenotypical and Neuropathological Features
21. PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype
22. MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia
23. Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia
24. P3-166: Epidemiology of Frontotemporal dementia in southern Italy
25. AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions
26. P3-286: Subcortical ischemic vascular dementia: A search for APP gene mutations
27. P3‐277: TAU V363I mutation: Pathogenic or not?
28. P3-279: A novel progranulin mutation in a large frontotemporal dementia calabrian kindred
29. P3-404: Presenilins mutations are frequent in early-onset familial frontotemporal dementia
30. P1-319: Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” AD
31. Epidemiology of Frontotemporal dementia in southern Italy
32. Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
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