All Stories

  1. Plasma levels of glial fibrillary acidic protein and neurofilament light chain in patients with chronic migraine: a multicenter case-control study
  2. Quantification of serum TDP-43 and neurofilament light chain in patients with amyotrophic lateral sclerosis stratified by UNC13A genotype
  3. Transcranial static magnetic stimulation for amyotrophic lateral sclerosis: a bicentric, randomised, double-blind placebo-controlled phase 2 trial
  4. QSM-detected iron accumulation in the cerebellar gray matter is selectively associated with executive dysfunction in non-demented ALS patients
  5. Further insights into anti-IgLON5 disease: a case with complex clinical presentation
  6. Prevalence and motor-functional correlates of frontotemporal-spectrum disorders in a large cohort of non-demented ALS patients
  7. Correction to: Assessing the Long-Term (48-Week) Effectiveness, Safety, and Tolerability of Fremanezumab in Migraine in Real Life: Insights from the Multicenter, Prospective, FRIEND3 Study
  8. Evaluating the Effectiveness, Tolerability, and Safety of Eptinezumab in High-Frequency and Chronic Migraine in Real World: EMBRACE—The First Italian Multicenter, Prospective, Real-Life Study
  9. Ecological validity of performance-based cognitive screeners in amyotrophic lateral sclerosis: preliminary evidence
  10. Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosis
  11. Assessing the Long-Term (48-Week) Effectiveness, Safety, and Tolerability of Fremanezumab in Migraine in Real Life: Insights from the Multicenter, Prospective, FRIEND3 Study
  12. Cervical motion alterations and brain functional connectivity in cervical dystonia
  13. Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial
  14. Longitudinal Feasibility of the Montreal Cognitive Assessment (MoCA) in Non-Demented ALS Patients
  15. A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS): the statistical analysis plan of TUDCA-ALS trial
  16. An exploratory study on counterfactual thinking in amyotrophic lateral sclerosis
  17. The value of routine blood work-up in clinical stratification and prognosis of patients with amyotrophic lateral sclerosis
  18. Frontotemporal-spectrum disorders and functional independence in non-demented ALS patients
  19. The impact of upper motor neuron involvement on clinical features, disease progression and prognosis in amyotrophic lateral sclerosis
  20. Correction: Clinimetrics and feasibility of the Italian version of the Frontal Assessment Battery (FAB) in non-demented Parkinson’s disease patients
  21. Bulbar involvement and cognitive features in amyotrophic lateral sclerosis: a retrospective study on 347 patients
  22. Phosphorylated tau in plasma could be a biomarker of lower motor neuron impairment in amyotrophic lateral sclerosis
  23. Single task-level, 2SD-based cutoffs for the Italian version of the Edinburgh Cognitive and Behavioral ALS screen (ECAS)
  24. Equating norms between the ALS Cognitive Behavioral Screen (ALS-CBS™) and the Edinburgh Cognitive and Behavioural ALS Screen (ECAS) in non-demented ALS patients
  25. Clinical usability of the Story-Based Empathy Task (SET) in non-demented ALS patients
  26. Clinimetrics and feasibility of the Italian version of the Frontal Assessment Battery (FAB) in non-demented Parkinson’s disease patients
  27. Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis
  28. Correction to: Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis
  29. Standardization of the Italian ALS-CBS™ Caregiver Behavioral Questionnaire
  30. Relationship between cerebrospinal fluid/serum albumin quotient and phenotype in amyotrophic lateral sclerosis: a retrospective study on 328 patients
  31. Correction to: A video of best practice recommendations for making botulinum toxin therapy safe during the COVID‑19 pandemic
  32. Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosis
  33. Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis
  34. Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: The TUDCA-ALS trial protocol
  35. Maintenance of response and predictive factors of 1‐year GalcanezumAb treatment in real‐life migraine patients in Italy : The multicenter prospective cohort GARLIT...
  36. Conversion from chronic to episodic migraine in patients treated with galcanezumab in real life in Italy: the 12-month observational, longitudinal, cohort multicenter GARLIT experience
  37. Ecological Validity of the Montreal Cognitive Assessment in Non-Demented Parkinson’s Disease Patients
  38. Rapid response to galcanezumab and predictive factors in chronic migraine patients: A 3‐month observational, longitudinal, cohort, multicenter, Italian real‐life study
  39. Validation of the DYALS (dysphagia in amyotrophic lateral sclerosis) questionnaire for the evaluation of dysphagia in ALS patients
  40. Exosome microRNAs in Amyotrophic Lateral Sclerosis: A Pilot Study
  41. Clinical features, disease progression, and use of healthcare resources in a large sample of 866 patients from 24 headache centers: A real‐life perspective from the Italian chROnic migraiNe (IRON) project
  42. Burden and attitude to resistant and refractory migraine: a survey from the European Headache Federation with the endorsement of the European Migraine & Headache Alliance
  43. Galcanezumab for the prevention of high frequency episodic and chronic migraine in real life in Italy: a multicenter prospective cohort study (the GARLIT study)
  44. Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis
  45. Structural MRI outcomes and predictors of disease progression in amyotrophic lateral sclerosis
  46. CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum
  47. Headaches in the emergency department –a survey of patients’ characteristics, facts and needs
  48. PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival
  49. The Complex Interplay Between Depression/Anxiety and Executive Functioning: Insights From the ECAS in a Large ALS Population
  50. Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutations
  51. Signaling between adipose and nervous tissues are altered in several neurodegenerative diseases
  52. The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS)
  53. Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts
  54. Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations