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4. A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

5. Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

6. Genetic variation inHIF1Ais associated with smoldering inflammation and disease progression in Multiple Sclerosis

7. Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

8. Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases.

9. Pilot Study on QTc Interval in Dogs Treated with Domperidone

11. Risk HLA Variants Affect the T-Cell Repertoire in Multiple Sclerosis

12. Genetic Variants in Iron Metabolism impact Disease Progression in MS through HIF1A (S9.006)

15. Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach

16. Intrinsic-Dimension Analysis for Guiding Dimensionality Reduction in Multi-Omics Data

17. A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility

19. Pleural Disease

20. Involvement of NINJ2 Protein in Inflammation and Blood–Brain Barrier Transmigration of Monocytes in Multiple Sclerosis

21. Clinical and pathological findings in neurolymphomatosis: Preliminary association with gene expression profiles in sural nerves

23. When it's neighbor's fault, a complicated ascending aortic aneurysm mimicking pulmonary embolism: A case report

24. COL6A5 variants in familial neuropathic chronic itch

25. A late spontaneous peripherally inserted central catheter migration: two cases series.

28. The Small RNA ErsA Impacts the Anaerobic Metabolism of Pseudomonas aeruginosa Through Post-Transcriptional Modulation of the Master Regulator Anr

34. Impact of multiple sclerosis risk loci in postinfectious neurological syndromes

35. Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population.

36. MOESM3 of Laser capture microdissection for transcriptomic profiles in human skin biopsies

37. Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.

38. A Whole-Exome Sequencing Study In Multiple Sclerosis Multiplex Families (P2.389)

39. COL6A5variants in familial neuropathic chronic itch

40. Bioinformatics molecular dynamics and docking pipeline analysis for high-throughput genome analysis and drug discovery oriented to personalized pain therapy in non-responsive patients

41. Role of PET-CT in the evaluation of early response to neoadjuvant treatment of locally advanced non-small cell lung cancer (NSCLC)

42. Radiation-induced lung disease (RILD) after 3D Conformal (3D-CRT) and Stereotactic Body Radiotherapy (SBRT) in patients treated for non-small cell lung cancer (NSCLC): correlation with dosimetric parameters and pulmonary function tests (PFTs)

43. Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction

44. Lung abnormalities at multimodality imaging after radiation therapy for non-small cell lung cancer

46. The vast majority of lymphocytes infiltrating primary cutaneous melanoma express the CD27 costimulatory receptor: implications for melanoma progression

48. Correction: Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.

49. Reliability and Usefulness of Random Fecal a1-Antitrypsin Concentration

50. Reliability and Usefulness of Random Fecal α1Antitrypsin Concentration

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