All Stories

  1. Limitations of Complement Activity Assays as Biomarkers for Ravulizumab Therapeutic Monitoring
  2. Localized Changes in Dentate Nucleus Shape and Magnetic Susceptibility in Friedreich Ataxia
  3. Expert consensus recommendations for improving and standardising the assessment of patients with generalised myasthenia gravis
  4. Refocusing generalized myasthenia gravis: Patient burden, disease profiles, and the role of evolving therapy
  5. Efficacy of innovative therapies in myasthenia gravis: A systematic review, meta‐analysis and network meta‐analysis
  6. Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence
  7. The C-Terminal Cross-linked Telopeptide of Type I Collagen (CTX-I) as a Potential Cardiomyopathy Biomarker in Friedreich Ataxia Patients
  8. Safety experience with continued exposure to ofatumumab in patients with relapsing forms of multiple sclerosis for up to 3.5 years
  9. Interplay Between Cognitive and Bowel/Bladder Function in Multiple Sclerosis
  10. A real‐world study of alemtuzumab in a cohort of Italian patients
  11. Switch from sequestering to anti-CD20 depleting treatment: disease activity outcomes during wash-out and in the first 6 months of ocrelizumab therapy
  12. First therapy choice in newly diagnosed Multiple Sclerosis patients: A multicenter Italian study
  13. Clinical predictors of Dimethyl Fumarate response in multiple sclerosis: a real life multicentre study
  14. Is antibody titer useful to verify the immunization after VZV Vaccine in MS patients treated with Fingolimod? A case series
  15. The use of medical grade cannabis in Italy for drug-resistant epilepsy: a case series
  16. The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families
  17. Overt hypogonadism may be not a sentinel sign of RNF216 : two novel mutations associated with ataxia, chorea and fertility
  18. Olfactory function and cognition in relapsing–remitting and secondary-progressive multiple sclerosis
  19. Bacterial and CMV pneumonia in a patient treated with alemtuzumab for multiple sclerosis
  20. Cognitive and functional connectivity alterations in Friedreich's ataxia
  21. Dissociative identity disorder: Restoration of executive functions after switch from alter to host personality
  22. Peripheral markers of autophagy in polyglutamine diseases
  23. The Multiple Faces of Spinocerebellar Ataxia type 2
  24. Normalization of timed neuropsychological tests with the PATA rate and nine-hole pegboard tests
  25. The iEDSS: BICAMS for the Cerebral Functional Score
  26. Lamivudine and fingolimod co-administration in two patients with multiple sclerosis and occult hepatitis B virus infection
  27. The use of medical-grade cannabis in patients non-responders to Nabiximols
  28. Mobitz type I and II atrioventricular blocks during fingolimod therapy
  29. Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia
  30. Modifications of resting state networks in spinocerebellar ataxia type 2
  31. Multiple hormone deficiencies in chronic heart failure
  32. The combined use of conventional MRI and MR spectroscopic imaging increases the diagnostic accuracy in amyotrophic lateral sclerosis
  33. A randomized controlled pilot trial of lithium in spinocerebellar ataxia type 2
  34. Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD)
  35. Safety of the first dose of fingolimod for multiple sclerosis: results of an open-label clinical trial
  36. Safety and tolerability of carbamylated erythropoietin in Friedreich's ataxia
  37. Genetic Screening for the LRRK2 R1441C and G2019S Mutations in Parkinsonian Patients from Campania
  38. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
  39. A Randomized, Double-blind, Placebo-Controlled Study of Latrepirdine in Patients With Mild to Moderate Huntington Disease
  40. Migraine attack restores the response of vascular smooth muscle cells to nitric oxide but not to norepinephrine
  41. Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene
  42. A randomized clinical trial of lithium in multiple system atrophy
  43. A gene expression phenotype in lymphocytes from friedreich ataxia patients
  44. A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal results
  45. A Combined Nucleic Acid and Protein Analysis in Friedreich Ataxia: Implications for Diagnosis, Pathogenesis and Clinical Trial Design
  46. Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit
  47. Benign hereditary chorea: Clinical and neuroimaging features in an Italian family
  48. Vascular smooth muscle cell dysfunction in patients with migraine
  49. SCA Functional Index: A useful compound performance measure for spinocerebellar ataxia
  50. Recombinant Human Erythropoietin Increases Frataxin Protein Expression Without Increasing mRNA Expression
  51. Ataxia with oculomotor apraxia type 2: A clinical, pathologic, and genetic study
  52. Novel mutation ofSACSgene in a Spanish family with autosomal recessive spastic ataxia
  53. Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation
  54. Very late onset in ataxia oculomotor apraxia type I