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1. Natalizumab treatment shows low cumulative probabilities of confirmed disability worsening to EDSS milestones in the long-term setting

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

7. The Italian multiple sclerosis register

21. Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: I: Fetal risks

22. Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: II: Maternal risks

25. C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson’s disease complicated by psychosis or dementia in a Sardinian population

28. Correction to: The Italian multiple sclerosis register

29. Natalizumab treatment and pregnancy in multiple sclerosis: A reappraisal of maternal and infant outcomes after 6 years

32. Guidelines on the clinical use for the detection of neutralizing antibodies (NAbs) to IFN beta in multiple sclerosis therapy: report from the Italian Multiple Sclerosis Study group

33. Guidelines from The Italian Neurological and Neuroradiological Societies for the use of magnetic resonance imaging in daily life clinical practice of multiple sclerosis patients

34. Multiple Sclerosis and Bipolar Disorders

35. Fingolimod versus interferon beta/glatiramer acetate after natalizumab suspension in multiple sclerosis

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

39. The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms

40. Pregnancy in multiple sclerosis women with relapses in the year before conception increases the risk of long-term disability worsening

41. Multicenter Interventional Phase IV Study for the Assessment of the Effects on Patient's Satisfaction of Peg IFN Beta-1a (Pre-filled Pen) in Subjects With Relapsing–Remitting Multiple Sclerosis Unsatisfied With Other Injectable Subcutaneous Interferons (PLATINUM Study)

42. ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

44. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charlote-Marie-Tooth and distal hereditary motor neuropathy

46. Postpartum relapses increase the risk of disability progression in multiple sclerosis: the role of disease modifying drugs

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

50. Long-term results of immunomodulatory treatment in children and adolescents with multiple sclerosis: the Italian experience

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