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191 results on '"Bartolomei Ilaria"'

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1. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

2. Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

3. Hypoperfusion of brain parenchyma is associated with the severity of chronic cerebrospinal venous insufficiency in patients with multiple sclerosis: a cross-sectional preliminary report

4. A seasonal periodicity in relapses of multiple sclerosis? A single-center, population-based, preliminary study conducted in Bologna, Italy

5. Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study

6. Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study

8. Familial Cardiac Amyloidoses

10. Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study

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

14. Withdrawal of mechanical ventilation in amyotrophic lateral sclerosis patients: a multicenter Italian survey.

17. Changes of Cine Cerebrospinal Fluid Dynamics in Patients with Multiple Sclerosis Treated with Percutaneous Transluminal Angioplasty: A Case-control Study

19. Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study

21. Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis

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

25. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

26. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

28. Genetic counselling in ALS: facts, uncertainties and clinical suggestions

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

32. 11 C‐PK11195 PET–based molecular study of microglia activation in SOD1 amyotrophic lateral sclerosis

33. ATTRv amyloidosis Italian Registry: clinical and epidemiological data

35. A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

37. Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum.

38. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

40. Additional file 6 of Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

41. Additional file 4 of Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

42. Additional file 5 of Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

43. Additional file 2 of Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

44. Additional file 1 of Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

45. FUS mutations in sporadic amyotrophic lateral sclerosis

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

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

48. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

49. Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

50. HFE p.H63D polymorphism does not influence ALS phenotype and survival

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