76 results on '"Confaloni, A."'
Search Results
2. The impact of a mono-institutional experience in lung metastases treated with stereotactic body radiation therapy (SBRT): a retrospective analysis
3. PO-1401 MR-guided adaptive versus CT-guided SBRT for prostate cancer: where is cost-benefit balance?
4. MR-guided adaptive versus CT-guided stereotactic radiotherapy for prostate cancer: Where is the best cost-benefit balance?
5. Circulating microRNAs in Neurodegenerative Diseases
6. Branched Chain Amino Acids in Experimental Models of Amyotrophic Lateral Sclerosis
7. A Sex Perspective in Neurodegenerative Diseases: microRNAs as Possible Peripheral Biomarkers
8. Activation of Tyrosine Phosphorylation Signaling in Erythrocytes of Patients with Alzheimer’s Disease
9. M2 Receptor Activation Counteracts the Glioblastoma Cancer Stem Cell Response to Hypoxia Condition
10. Dietary Lipids: Exogenous Control of Myelination
11. Plasma microRNA profiling distinguishes patients with frontotemporal dementia from healthy subjects
12. Role of non-echo-planar diffusion-weighted images in the identification of recurrent cholesteatoma of the temporal bone
13. MicroRNAs and mild cognitive impairment: A systematic review
14. Differentiation-Dependent Effects of a New Recombinant Manganese Superoxide Dismutase on Human SK-N-BE Neuron-Like Cells
15. Heme Oxygenase-1 and Brain Oxysterols Metabolism Are Linked to Egr-1 Expression in Aged Mice Cortex, but Not in Hippocampus
16. Circulating miR-127-3p as a Potential Biomarker for Differential Diagnosis in Frontotemporal Dementia
17. Outcomes of postoperative stereotactic radiosurgery to the resection cavity versus stereotactic radiosurgery alone for melanoma brain metastases
18. Reduced miR-659-3p Levels Correlate with Progranulin Increase in Hypoxic Conditions: Implications for Frontotemporal Dementia
19. Protocols for Application of Non-EPI DW MRI in Cholesteatoma
20. Promising Therapies for Alzheimer';s Disease
21. Frontotemporal Lobar Degeneration and MicroRNAs
22. PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population
23. SORL1 Gene is Associated with the Conversion from Mild Cognitive Impairment to Alzheimer’s Disease
24. Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
25. Neuropsychological predictors of rapidly progressive Alzheimer's disease
26. External Factors and Myelin Assembly
27. Binge eating and fast cognitive worsening in an early-onset bvFTD patient carrying C9ORF72 expansion
28. Circulating miRNAs as Biomarkers for Neurodegenerative Disorders
29. Familial Alzheimer's disease sustained by presenilin 2 mutations: Systematic review of literature and genotype–phenotype correlation
30. Thapsigargin affects presenilin-2 but not presenilin-1 regulation in SK-N-BE cells
31. Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation
32. Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors
33. Gender Effects on Plasma PGRN Levels in Patients with Alzheimer's Disease: A Preliminary Study
34. Gender differences in Parkinson’s disease: focus on plasma alpha-synuclein
35. Sex effect on presenilins expression in post-natal rat brain
36. Increased levels of acute-phase inflammatory proteins in plasma of patients with sporadic CJD
37. T lymphocytes from patients with systemic lupus erythematosus are resistant to induction of autophagy
38. Replication Study to Confirm the Role of CYP2D6 Polymorphism rs1080985 on Donepezil Efficacy in Alzheimer's Disease Patients
39. P1-282: Annamaria Confaloni PhD
40. Presenilin 2 mutation R71W in an Italian early-onset sporadic Alzheimer’s disease case
41. Altered oxidative stress profile in the cortex of mice fed an enriched branched-chain amino acids diet: Possible link with amyotrophic lateral sclerosis?
42. Rosuvastatin and Thapsigargin Modulate γ-Secretase Gene Expression and APP Processing in a Human Neuroglioma Model
43. A Novel Mutation in the Predicted TMIII Domain of the PSEN2 Gene in an Italian Pedigree with Atypical Alzheimer's Disease
44. The London APP Mutation (Val717Ile) Associated with Early Shifting Abilities and Behavioral Changes in Two Italian Families with Early-Onset Alzheimer’s Disease
45. P4‐122: Italian presenilin 2 mutation (R71W) in early‐onset dementia with relevant behavioural disturbances
46. P1‐071: Familial and sporadic Alzheimer's disease: A clinical longitudinal study
47. Gene Expression Profiles of APP and BACE1 in Tg SOD1G93A Cortical Cells
48. P3-251: A novel Italian presenilin 2 mutation (S175Y)
49. A novel PSEN2 mutation associated with a peculiar phenotype
50. Altered expression of cyclooxygenase-2, presenilins and oxygen radical scavenging enzymes in a rat model of global perinatal asphyxia
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