References

Neurophysiologic studies in Morvan syndrome

10.1097/00004691-200411000-00008 · 2004 · External reference

Pediatric LGI1 and CASPR2 autoimmunity associated with COVID-19: Morvan syndrome

10.1007/s00415-021-10614-6 · 2021 · External reference

Morvan’s syndrome presenting with psychiatric manifestations: a case report and review of the literature

10.4103/0028-3886.349616 · 2022 · External reference

Differentiating oneiric stupor in agrypnia excitata from dreaming disorders

10.3389/fneur.2020.565694 · 2020 · External reference

Morvan syndrome: clinical and serological observations in 29 cases

10.1002/ana.23577 · 2012 · External reference

CASPR2-related Morvan syndrome: autonomic, polysomnographic, and neuropsychological observations

10.1212/cpj.0000000000000978 · 2021 · External reference

Autoimmune neuromyotonia

10.1097/wco.0000000000001104 · 2022 · External reference

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

10.1016/s0896-6273(00)81049-1 · 1999 · External reference

Pathophysiological effects of autoantibodies in autoimmune encephalitides

10.3390/cells13010015 · 2023 · External reference

Acquired neuromyotonia in thymoma-associated myasthenia gravis: a clinical and serological study

10.1111/ene.13922 · 2019 · External reference

Case report: anti-LGI1 encephalitis following COVID-19 vaccination

10.3389/fimmu.2021.813487 · 2022 · External reference

Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia

10.1093/brain/awq213 · 2010 · External reference

The clinical spectrum of Caspr2 antibody-associated disease

10.1212/wnl.0000000000002917 · 2016 · External reference

A rare case of peripheral nerve hyperexcitability in childhood: Isaacs syndrome

10.4103/jpn.jpn_128_19 · 2020 · External reference