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Clinical, biological, electrophysiological and therapeutic profile of patients with anti-MAG neuropathy according to MYD88 L265P and CXCR4 mutations and underlying haemopathy.

Alexandre GuérémyJosé BoucrautJohn BoudjaraneAude-Marie GrapperonEtienne FortanierLaure FarnaultJean GabertFrédéric VelyRomaric LacroixLudivine KoutonShahram AttarianEmilien Delmont
Published in: Journal of neurology (2023)
mutation and underlying haemopathies are not predictive of a more severe disease. However, in cases of resistant and progressive neuropathy, they provide an opportunity to prescribe newly available drugs such as Bruton tyrosine kinase inhibitors.
Keyphrases
  • multiple sclerosis
  • toll like receptor
  • early onset
  • drug induced
  • immune response