All Stories

  1. Blood DNA Methylation in Nuclear and Mitochondrial Sequences Links to Malnutrition and Poor Prognosis in ALS: A Longitudinal Study
  2. Guía práctica de diagnóstico y manejo en la enfermedad de Charcot-Marie-Tooth en España
  3. Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study
  4. Description of clinical and genetic features of 122 patients included in the Spanish Pompe registry
  5. Miastenia gravis. Actualización diagnóstica y terapéutica
  6. Mapa epidemiológico transversal de las ataxias y paraparesias espásticas hereditarias en España
  7. CSF Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barré Syndrome
  8. Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease
  9. Epidemiología de la miastenia grave en la península ibérica y Latinoamérica
  10. Cumulative genetic risk andC9orf72repeat status independently associate with ALS status in two case-control studies
  11. An International Perspective on Preceding Infections in Guillain-Barré Syndrome
  12. Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values
  13. International Validation of the Erasmus Guillain–Barré Syndrome Respiratory Insufficiency Score
  14. Predicting Outcome in Guillain-Barré Syndrome
  15. Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome
  16. Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy
  17. Autoantibody screening in Guillain–Barré syndrome
  18. Autoantibody screening in Guillain-Barré Syndrome
  19. Clinical characteristics and outcomes of thymoma‐associated myasthenia gravis
  20. Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4
  21. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barré syndrome patients
  22. Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)
  23. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barré syndrome patients
  24. Clinical and therapeutic features of myasthenia gravis in adults based on age at onset
  25. Respuesta clínica y neurofisiológica a la efedrina en un paciente con síndrome miasténico congénito de canal lento
  26. Current treatment practice of Guillain-Barré syndrome
  27. Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
  28. Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations
  29. Regional variation of Guillain-Barré syndrome
  30. Inflammatory myopathy in the context of an unusual overlapping laminopathy
  31. The impact of rituximab infusion protocol on the long-term outcome in anti-MuSK myasthenia gravis
  32. Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15
  33. Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
  34. Phenotypical features of a new dominant GDAP1 pathogenic variant (p.R226del) in axonal Charcot-Marie-Tooth disease
  35. International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome
  36. PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36
  37. Guillain-Barré syndrome following the 2009 pandemic monovalent and seasonal trivalent influenza vaccination campaigns in Spain from 2009 to 2011: outcomes from active surveillance by a neurologist network, and records from a country-wide hospital disch...
  38. Rituximab in treatment-resistant CIDP with antibodies against paranodal proteins
  39. Analysis of theCHCHD10gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
  40. Gastrointestinal symptoms in late-onset Pompe disease: Early response to enzyme replacement therapy
  41. Neuropatías, radiculopatías y plexopatías
  42. Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry
  43. Successful treatment of hypokalemic periodic paralysis with topiramate
  44. Can we predict the response in the treatment of epilepsy with vagus nerve stimulation?
  45. Levetiracetam following liver and kidney failure in late-onset anticonvulsant hypersensitivity syndrome
  46. Long-term outcome in chronic inflammatory demyelinating polyneuropathy patients treated with intravenous immunoglobulin: A retrospective study
  47. A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis
  48. Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
  49. Diagnóstico y tratamiento del dolor neuropático
  50. Two-stage case-control association study of dopamine-related genes and migraine
  51. Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation
  52. Public health surveillance and incidence of adulthood Guillain-Barré syndrome in Spain, 1998–1999: the view from a sentinel network of neurologists
  53. Guillain-Barré Syndrome in Spain, 1985–1997: Epidemiological and Public Health Views
  54. P134 Electroneurographic (ENoG) evaluation of peripheral facial palsy (PFP). Early and late results in 500 patients
  55. Bone anomalies in myotonic dystrophy