z-logo
open-access-imgOpen Access
Acquired Neuromyotonia Heralding Recurrent Thymoma in Myasthenia Gravis
Author(s) -
Jori Fleisher,
Megan Richie,
Raymond S. Price,
Steven S. Scherer,
Josep Dalmau,
Eric Lancaster
Publication year - 2013
Publication title -
jama neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.298
H-Index - 231
eISSN - 2168-6157
pISSN - 2168-6149
DOI - 10.1001/jamaneurol.2013.2863
Subject(s) - neuromyotonia , thymoma , myasthenia gravis , thymectomy , medicine , thymus neoplasm , gastroenterology , pathology , antibody , immunology
Acquired neuromyotonia is increasingly recognized as an autoimmune disorder, frequently associated with antibodies against voltage-gated potassium channel complex proteins.We present a case of acquired neuromyotonia as the heralding symptom of recurrent thymoma in a patient with myasthenia gravis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom