46 results on '"Petrozzi, Lucia"'
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2. Nrf2 Signaling: An Adaptive Response Pathway for Neurodegenerative Disorders
3. Biological determinants of blood‐based cytokines in the Alzheimer's disease clinical continuum
4. Comparison of plasmatic interleukins patterns among cognitively unimpaired subjects, patients affected by mild cognitive impairment and subjects with Alzheimer's disease dementia
5. α-Synuclein Heteromers in Red Blood Cells of Alzheimer’s Disease and Lewy Body Dementia Patients
6. Red blood cell α‐synuclein heteroaggregates can discriminate healthy controls from cognitively impaired subjects of the AD‐LBD spectrum
7. Sex differences in red blood cell α ‐synuclein protein and its heteroaggregates with amyloid‐β and tau in early Alzheimer’s disease
8. α-Synuclein heteromers with ß-amyloid and tau decreased in red blood cells of Alzheimer’s disease and Lewy Body dementia patients.
9. Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
10. P2-239: POTENTIAL DIAGNOSTIC VALUE OF RED BLOOD CELLS α-SYNUCLEIN HETEROAGGREGATES IN ALZHEIMER'S DISEASE
11. Potential Diagnostic Value of Red Blood Cells α-Synuclein Heteroaggregates in Alzheimer’s Disease
12. Amyotrophic Lateral Sclerosis and Oxidative Stress: A Double-Blind Therapeutic Trial After Curcumin Supplementation
13. α-Synuclein Heterocomplexes with β-Amyloid Are Increased in Red Blood Cells of Parkinson’s Disease Patients and Correlate with Disease Severity
14. α-Synuclein Aggregated with Tau and β-Amyloid in Human Platelets from Healthy Subjects: Correlation with Physical Exercise
15. A single center study: Aβ42/p-Tau181 CSF ratio to discriminate AD from FTD in clinical setting
16. α-Synuclein Aggregates with β-Amyloid or Tau in Human Red Blood Cells: Correlation with Antioxidant Capability and Physical Exercise in Human Healthy Subjects
17. Gly482Ser PGC-1α Gene Polymorphism and Exercise-Related Oxidative Stress in Amyotrophic Lateral Sclerosis Patients
18. Methylation analysis of multiple genes in blood DNA of Alzheimer’s disease and healthy individuals
19. Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington’s Disease
20. Lack of Association between Nuclear Factor Erythroid-Derived 2-Like 2 Promoter Gene Polymorphisms and Oxidative Stress Biomarkers in Amyotrophic Lateral Sclerosis Patients
21. Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: A case report and an update on the state of art
22. An “inflammatory” mitochondrial myopathy. A case report
23. Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatment
24. Nerve and muscle involvement in mitochondrial disorders: an electrophysiological study
25. A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia
26. The hOGG1 Ser326Cys polymorphism and Huntington's disease
27. Clock T3111C and Per2 C111G SNPs do not influence circadian rhythmicity in healthy Italian population
28. Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation
29. Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype
30. The mtDNA A8344G “MERRF” mutation is not a common cause of sporadic Parkinson disease in Italian population
31. Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genes
32. Mitochondria and Neurodegeneration
33. Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis
34. A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease
35. MERRF syndrome without ragged-red fibers: The need for molecular diagnosis
36. Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseases
37. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
38. Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis ofSPG4 reveals eleven novel mutations
39. Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations
40. Elevated levels of oxidative DNA damage in patients with coronary artery disease
41. Chromosome and oxidative damage biomarkers in lymphocytes of Parkinson's disease patients
42. Diurnal Motor Variations to Repeated Doses of Levodopa in Parkinson's Disease
43. Effects of chronic long-term therapy with calcium antagonists on cytogenetic damage in humans
44. Pharmacokinetics and Pharmacodynamics of L-DOPA After Acute and 6-Week Tolcapone Administration in Patients with Parkinsonʼs Disease
45. Spontaneous and induced aneuploidy in peripheral blood lymphocytes of patients with Alzheimer's disease
46. P XIII.20 A family study of baseline chromosomal aberration and sister chromatid exchange frequencies
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