163 results on '"Petrozzi, Lucia"'
Search Results
2. Potential Diagnostic Value of Red Blood Cells α-Synuclein Heteroaggregates in Alzheimer’s Disease
3. α-Synuclein Aggregates with β-Amyloid or Tau in Human Red Blood Cells: Correlation with Antioxidant Capability and Physical Exercise in Human Healthy Subjects
4. A single center study: Aβ42/p-Tau181 CSF ratio to discriminate AD from FTD in clinical setting
5. Nrf2 Signaling: An Adaptive Response Pathway for Neurodegenerative Disorders
6. Biological determinants of blood‐based cytokines in the Alzheimer's disease clinical continuum
7. Comparison of plasmatic interleukins patterns among cognitively unimpaired subjects, patients affected by mild cognitive impairment and subjects with Alzheimer's disease dementia
8. The hOGG1 Ser326Cys polymorphism and Huntington's disease
9. Nerve and muscle involvement in mitochondrial disorders: an electrophysiological study
10. Clock T3111C and Per2 C111G SNPs do not influence circadian rhythmicity in healthy Italian population
11. Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation
12. α-Synuclein Heteromers in Red Blood Cells of Alzheimer’s Disease and Lewy Body Dementia Patients
13. Mitochondria and Neurodegeneration
14. Red blood cell α‐synuclein heteroaggregates can discriminate healthy controls from cognitively impaired subjects of the AD‐LBD spectrum
15. Sex differences in red blood cell α ‐synuclein protein and its heteroaggregates with amyloid‐β and tau in early Alzheimer’s disease
16. α-Synuclein heteromers with ß-amyloid and tau decreased in red blood cells of Alzheimer’s disease and Lewy Body dementia patients.
17. Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
18. Spontaneous and induced aneuploidy in peripheral blood lymphocytes of patients with Alzheimer’s disease
19. Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinsonʼs disease
20. Spontaneous and induced chromosome damage in somatic cells of sporadic and familial Alzheimerʼs disease patients
21. P2-239: POTENTIAL DIAGNOSTIC VALUE OF RED BLOOD CELLS α-SYNUCLEIN HETEROAGGREGATES IN ALZHEIMER'S DISEASE
22. Chromosome and oxidative damage biomarkers in lymphocytes of Parkinson's disease patients
23. Amyotrophic Lateral Sclerosis and Oxidative Stress: A Double-Blind Therapeutic Trial After Curcumin Supplementation
24. α-Synuclein Heterocomplexes with β-Amyloid Are Increased in Red Blood Cells of Parkinson’s Disease Patients and Correlate with Disease Severity
25. α-Synuclein Aggregated with Tau and β-Amyloid in Human Platelets from Healthy Subjects: Correlation with Physical Exercise
26. α-Synuclein Aggregates with β-Amyloid or Tau in Human Red Blood Cells: Correlation with Antioxidant Capability and Physical Exercise in Human Healthy Subjects
27. Gly482Ser PGC-1α Gene Polymorphism and Exercise-Related Oxidative Stress in Amyotrophic Lateral Sclerosis Patients
28. Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatment
29. Tetracycline treatment in patients with progressive external ophthalmoplegia
30. Methylation analysis of multiple genes in blood DNA of Alzheimer’s disease and healthy individuals
31. Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington’s Disease
32. A novel mitochondrial tRNA Ile point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia
33. A single center study: Aβ42/p-Tau181 CSF ratio to discriminate AD from FTD in clinical setting.
34. NEWS and VIEWS: mitochondrial encephalomyopathies.
35. Lack of Association between Nuclear Factor Erythroid-Derived 2-Like 2 Promoter Gene Polymorphisms and Oxidative Stress Biomarkers in Amyotrophic Lateral Sclerosis Patients
36. Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: A case report and an update on the state of art
37. An “inflammatory” mitochondrial myopathy. A case report
38. Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.
39. Nerve and muscle involvement in mitochondrial disorders: an electrophysiological study
40. A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia
41. Clock T3111C and Per2 C111G SNPs do not influence circadian rhythmicity in healthy Italian population
42. Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation
43. Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype
44. The mtDNA A8344G “MERRF” mutation is not a common cause of sporadic Parkinson disease in Italian population
45. Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genes
46. Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis
47. A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease
48. MERRF syndrome without ragged-red fibers: The need for molecular diagnosis
49. Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseases
50. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.