All Stories

  1. Current treatment practice of Guillain-Barré syndrome
  2. Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
  3. Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations
  4. Regional variation of Guillain-Barré syndrome
  5. Inflammatory myopathy in the context of an unusual overlapping laminopathy
  6. The impact of rituximab infusion protocol on the long-term outcome in anti-MuSK myasthenia gravis
  7. Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15
  8. Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
  9. Phenotypical features of a new dominant GDAP1 pathogenic variant (p.R226del) in axonal Charcot-Marie-Tooth disease
  10. 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
  11. PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36
  12. 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...
  13. Rituximab in treatment-resistant CIDP with antibodies against paranodal proteins
  14. Analysis of theCHCHD10gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
  15. Gastrointestinal symptoms in late-onset Pompe disease: Early response to enzyme replacement therapy
  16. Neuropatías, radiculopatías y plexopatías
  17. Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry
  18. Long-term outcome in chronic inflammatory demyelinating polyneuropathy patients treated with intravenous immunoglobulin: A retrospective study
  19. A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis
  20. Diagnóstico y tratamiento del dolor neuropático
  21. Two-stage case-control association study of dopamine-related genes and migraine
  22. Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutation
  23. Public health surveillance and incidence of adulthood Guillain-Barré syndrome in Spain, 1998–1999: the view from a sentinel network of neurologists
  24. Guillain-Barré Syndrome in Spain, 1985–1997: Epidemiological and Public Health Views
  25. P134 Electroneurographic (ENoG) evaluation of peripheral facial palsy (PFP). Early and late results in 500 patients
  26. Bone anomalies in myotonic dystrophy