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75 results on '"Salvi, F"'

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1. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

2. Effects of Venous Angioplasty on Cerebral Lesions in Multiple Sclerosis: Expanded Analysis of the Brave Dreams Double-Blind, Sham-Controlled Randomized Trial

3. A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements

4. The MITOS system predicts long-term survival in amyotrophic lateral sclerosis

5. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

6. Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy

7. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

8. Autologous haematopoietic stem cell transplantation with an intermediate intensity conditioning regimen in multiple sclerosis: the Italian multi-centre experience

9. Serum IgG against Simian Virus 40 antigens are hampered by high levels of sHLA-G in patients affected by inflammatory neurological diseases, as multiple sclerosis

10. Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behcet's disease and deep vein thrombosis

11. Stereotactic Radiotherapy in the Treatment of Lung Metastases from Bone and Soft-tissue Sarcomas

12. Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

13. Assessment of White Matter Tract Damage in Patients with Amyotrophic Lateral Sclerosis: A Diffusion Tensor MR Imaging Tractography Study

14. MRI predictors of long-term evolution in amyotrophic lateral sclerosis

15. Dose-dense and high-dose chemotherapy plus rituximab with autologous stem cell transplantation for primary treatment of diffuse large B-cell lymphoma with a poor prognosis: A phase II multicenter study

16. Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

17. Vascular endothelial growth factor gene polymorphisms in Behçet's disease

18. PBSC mobilization in lymphoma patients: analysis of risk factors for collection failure and development of a predictive score based on the kinetics of circulating CD34+ cells and WBC after chemotherapy and G-CSF mobilization

19. Cerebrospinal fluid findings in Devic?s neuromyelitis optica

20. CSF dynamics and brain volume in multiple sclerosis are associated with extracranial venous flow anomalies: a pilot study

21. Use of neck magnetic resonance venography, Doppler sonography and selective venography for diagnosis of chronic cerebrospinal venous insufficiency: a pilot study in multiple sclerosis patients and healthy controls

22. Toll-like receptor 4 (TLR4) gene polymorphisms in Italian patients with Behçet's disease

23. Chronic cerebrospinal venous insufficiency in patients with multiple sclerosis

24. Autoantibodies in multiple sclerosis patients before and during IFN-beta 1b treatment: are they correlated with the occurrence of autoimmune diseases?

25. Intercellular adhesion molecule-1 gene polymorphisms in Behçet's Disease

26. Association of MICA alleles and HLA-B51 in Italian patients with Behçet's disease

27. Idarubicin in patients with diffuse large cell lymphomas: a randomized trial comparing VACOP-B (A= Doxorubicin) vs VICOP-B (I=Idarubicin)

28. Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study

29. Magnetization transfer and diffusion tensor MR imaging of acute disseminated encephalomyelitis

30. Multicenter case-control study on restless legs syndrome in multiple sclerosis: The REMS Study

31. Clinical manifestations of Behçet's disease in 137 Italian patients: Results of a multicenter study

32. Familial amyloid polyneuropathy: report of a family

33. Endothelial nitric oxide synthase gene polymorphisms in Behçet's disease

34. An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p

35. Protein Z G79A and A-13G gene polymorphisms in Italian patients with Behçet's disease

36. The severity of chronic cerebrospinal venous insufficiency in patients with multiple sclerosis is related to altered cerebrospinal fluid dynamics

37. Chronic cerebrospinal venous insufficiency and iron deposition on susceptibility-weighted imaging in patients with multiple sclerosis: A pilot case-control study

38. Antibiotic Use and Risk of Multiple Sclerosis: A Nested Case-Control Study in Emilia-Romagna Region, Italy

39. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

40. Differences among young adults, adults and elderly chronic myeloid leukemia patients

41. Small Fiber Neuropathy in Patients with Chronic Pain and a Previous Diagnosis of Multiple Chemical Sensitivity Syndrome

42. Combined heart and liver transplantation in four adults with familial amyloidosis: experience of a single center

43. The m.3890GA/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypes

44. Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

45. Assessment of Brain White Matter Fiber Bundle Atrophy in Patients with Friedreich Ataxia

46. Prognostic Evaluation of Disease Outcome in Solid Tumors Investigated With 64Cu-ATSM PET/CT

47. Neuropathy in multiple myeloma treated with thalidomide: A prospective study

48. Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study

49. Efficacy and Safety of Extracranial Vein Angioplasty in Multiple Sclerosis

50. Genotypic and phenotypic correlation in an Italian population of hereditary amyloidosis TTR-related (HA-TTR): clinical and neurophysiological aids to diagnosis and some reflections on misdiagnosis

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