203 results on '"Catania, Marcella"'
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2. Aβ1-6A2V(D) peptide, effective on Aβ aggregation, inhibits tau misfolding and protects the brain after traumatic brain injury
3. Spontaneous intracerebral haemorrhage associated with early-onset cerebral amyloid angiopathy and Alzheimer’s disease neuropathological changes five decades after cadaveric dura mater graft
4. A novel bio-inspired strategy to prevent amyloidogenesis and synaptic damage in Alzheimer’s disease
5. Serpin Signatures in Prion and Alzheimer’s Diseases
6. Exploring the ability of plasma pTau217, pTau181 and beta-amyloid in mirroring cerebrospinal fluid biomarker profile of Mild Cognitive Impairment by the fully automated Lumipulse® platform.
7. The novel I213S mutation in PSEN1 gene is located in a hotspot codon associated with familial early-onset Alzheimer's disease
8. Singular cases of Alzheimer’s disease disclose new and old genetic “acquaintances”
9. Autophagy Markers Are Altered in Alzheimer’s Disease, Dementia with Lewy Bodies and Frontotemporal Dementia
10. Rare causes of dystonia-parkinsonism with cognitive impairment, behavioral abnormalities, and voiceless whispering stereotypies: Describing the long-term evolution of the neurological phenotype in a patient with the PSEN2 Ile149Thr variant
11. Myoclonus in genetic Alzheimer’s disease due to Presenilin-1 mutation
12. One or more β-amyloid(s)? New insights into the prion-like nature of Alzheimer's disease
13. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene
14. Iatrogenic early onset cerebral amyloid angiopathy 30 years after cerebral trauma with neurosurgery: vascular amyloid deposits are made up of both Aβ40 and Aβ42
15. Corrigendum: PMCA-based detection of prions in the olfactory mucosa of patients with sporadic Creutzfeldt–Jakob disease
16. Expression of A2V-mutated Aβ in Caenorhabditis elegans results in oligomer formation and toxicity
17. Rac1 activation links tau hyperphosphorylation and Aβ dysmetabolism in Alzheimer’s disease
18. Good gene, bad gene: New APP variant may be both
19. SORL1gene mutation and octapeptide repeat insertion inPRNPgene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy
20. A novel bio-inspired strategy to prevent amyloidogenesis and synaptic damage in Alzheimer’s disease
21. A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis
22. PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt–Jakob Disease
23. Extra-repeat insertional mutation in the PRNP gene with cerebral amyloid angiopathy: A case report
24. Cerebrospinal Fluid EV Concentration and Size Are Altered in Alzheimer’s Disease and Dementia with Lewy Bodies
25. Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer’s Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene
26. SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy.
27. APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38
28. Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features
29. Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease
30. Plasma Extracellular Vesicle Size and Concentration Are Altered in Alzheimer’s Disease, Dementia With Lewy Bodies, and Frontotemporal Dementia
31. Microglial Heterogeneity and Its Potential Role in Driving Phenotypic Diversity of Alzheimer’s Disease
32. Chapter Nine - One or more β-amyloid(s)? New insights into the prion-like nature of Alzheimer's disease
33. Cerebral amyloid angiopathy in a 51-year-old patient with embolization by dura mater extract and surgery for nasopharyngeal angiofibroma at age 17
34. Singular cases of Alzheimer’s disease disclose new and old genetic “acquaintances”
35. Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
36. A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis
37. Diagnostic accuracy of prion disease biomarkers in iatrogenic Creutzfeldt-Jakob disease
38. Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project
39. Additional file 1: of Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene
40. Dreaming of a New World Where Alzheimer’s Is a Treatable Disorder
41. Familial frontotemporal dementia associated with the novel MAPT mutation T427M
42. Additional file 1: of Rac1 activation links tau hyperphosphorylation and Aβ dysmetabolism in Alzheimer’s disease
43. Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project.
44. Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38
45. Effects of peptidyl-prolyl isomerase 1 depletion in animal models of prion diseases
46. Molecular subtypes of Alzheimer’s disease
47. Altered Expression of Circulating Cdc42 in Frontotemporal Lobar Degeneration
48. Characterization of Amyloid-β Deposits in Bovine Brains
49. Tackling amyloidogenesis in Alzheimer’s disease with A2V variants of Amyloid-β
50. Anti-amyloidogenicactivity of a mutant form of Aβ: a new strategy for Alzheimer therapy
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