362 results on '"Melone, Mariarosa Anna Beatrice"'
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2. Human blood lipid profiles after dietary supplementation of different omega 3 ethyl esters formulations
3. POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients
4. A rapid, safe, and quantitative in vitro assay for measurement of uracil-DNA glycosylase activity
5. Sagittal kinematics and imbalance of the spine and whole body during walking in late-onset Pompe disease
6. First study on the peptidergic innervation of the brain superior sagittal sinus in humans
7. A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
8. Truncated Analogues of a G-Quadruplex-Forming Aptamer Targeting Mutant Huntingtin: Shorter Is Better!
9. The carnitine system and cancer metabolic plasticity
10. RETRACTED ARTICLE: Verapamil Inhibits Ser202/Thr205 Phosphorylation of Tau by Blocking TXNIP/ROS/p38 MAPK Pathway
11. Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype
12. Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network
13. Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix
14. Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression
15. Fighting the Huntington’s Disease with a G-Quadruplex-Forming Aptamer Specifically Binding to Mutant Huntingtin Protein: Biophysical Characterization, In Vitro and In Vivo Studies
16. Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4
17. A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
18. Neurofibromatosis type 1: Molecular spectrum of the NF1 mutations in a large cohort of adult Italian patients
19. Expression profiling of circulating miRNA in the Neurofibromatosis type 1 and related cancers in a large NF1 Italian cohort
20. Nanoparticle-Guided Brain Drug Delivery: Expanding the Therapeutic Approach to Neurodegenerative Diseases
21. Quantitative Evaluation of Upright Posture by x-Ray and 3D Stereophotogrammetry with a New Marker Set Protocol in Late Onset Pompe Disease
22. POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients
23. Short and long term effects of Nabiximols on balance and walking assessed by 3D-gait analysis in people with Multiple Sclerosis and spasticity.
24. “Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy
25. “One Health” Approach for Health Innovation and Active Aging in Campania (Italy)
26. Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement
27. Novel autophagic vacuolar myopathies: Phenotype and genotype features
28. Quantitative Evaluation of Upright Posture by X-Ray and 3D Stereophotogrammetry With an Original Marker Placement Protocol in Late Onset Pompe Disease.
29. Understanding the Biological Activities of Vitamin D in Type 1 Neurofibromatosis: New Insights into Disease Pathogenesis and Therapeutic Design
30. The Discovery of Highly Potent THP Derivatives as OCTN2 Inhibitors: From Structure-Based Virtual Screening to In Vivo Biological Activity
31. Bioactive Phenolic Compounds in the Modulation of Central and Peripheral Nervous System Cancers: Facts and Misdeeds
32. P32. Vacuolated pas-positive lymphocytes: a screening test for pompe disease and other autophagic myopathies
33. Nanotechnology-Based Polyphenol Delivery: A Novel Therapeutic Strategy for the Treatment of Age-Related Neurodegenerative Disorder
34. Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis
35. The carnitine system and cancer metabolic plasticity review-article
36. The Autophagy Signaling Pathway: A Potential Multifunctional Therapeutic Target of Curcumin in Neurological and Neuromuscular Diseases
37. Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
38. A case of Foix–Chavany–Marie syndrome due to bilateral corona radiata infarcts
39. Early posterior vitreous detachment is associated with LAMA5 dominant mutation
40. The Role of Cathepsin D in the Pathogenesis of Human Neurodegenerative Disorders
41. Neuro-Behçet’s disease presenting as an isolated progressive cognitive and behavioral syndrome
42. Meldonium improves Huntington’s disease mitochondrial dysfunction by restoring peroxisome proliferator‐activated receptor γ coactivator 1α expression
43. Metabolic syndrome, Mediterranean diet, and polyphenols: Evidence and perspectives
44. Neurofibromatous neuropathy: An ultrastructural study
45. Successful long-term therapy with flecainide in a family with paramyotonia congenita
46. Verapamil Inhibits Ser202/Thr205 Phosphorylation of Tau by Blocking TXNIP/ROS/p38 MAPK Pathway
47. A novel and rapid method of determining truncated neurofibromin 1 to rapidly screen for neurofibromatosis type 1 (NF1)
48. Protective effects of modified Mediterranean diet in patients with Parkinson's disease
49. Rasagiline improves sleep disorders in Parkinson's disease
50. Intracranial calcifications, parkinsonism and metabolic myopathy in disorder of calcium metbolism
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