42 results on '"Sassi, Celeste"'
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2. TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients
3. Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of Apulia
4. PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice
5. Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy
6. Investigating APOE, APP-Aβ metabolism genes and Alzheimer’s disease GWAS hits in brain small vessel ischemic disease
7. Shared and oppositely regulated transcriptomic signatures in Huntington's disease and brain ischemia confirm known and unveil novel potential neuroprotective genes
8. An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models
9. Persistent hiccups as main COVID-19 manifestation with transient cytotoxic lesion of the corpus callosum splenium during the Omicron wave in the post-vaccination era
10. TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients
11. Long-Term Connectome Analysis Reveals Reshaping of Visual, Spatial Networks in a Model With Vascular Dementia Features
12. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3
13. ABCA7 p.G215S as potential protective factor for Alzheimer's disease
14. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
15. Vascular cognitive impairment in the mouse reshapes visual, spatial network functional connectivity
16. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease
17. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease
18. TREM2 Variants in Alzheimerʼs Disease
19. Genetics of Parkinson Disease
20. Missense variant in TREML2 protects against Alzheimer's disease
21. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease:critical influence of CSF1R and NOTCH3
22. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3
23. White matter hyperintensities and neurodegenerative dementias
24. An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models
25. Additional file 1: of Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimerâ s disease resilience
26. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3
27. Correction: Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO)
28. Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO)
29. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease
30. ABCA7 p.G215S as potential protective factor for Alzheimer's disease
31. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease
32. A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy
33. Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience.
34. Genetics of Parkinson Disease
35. A Novel Splice Site Mutation in GRN (p.A237fs [A>T]) in a Large Italian Family With FTD From The Apulia-FTD Registry (P2.160)
36. A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production
37. LINKAGE AND WHOLE GENOME SEQUENCE ANALYSIS OF ALZHEIMER'S DISEASE RESILIENCE AND RISK
38. Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
39. Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.
40. ABCA7 p.G215S as potential protective factor for Alzheimer's disease
41. ABCA7 p.G215S as potential protective factor for Alzheimer's disease.
42. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.
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