Myasthenia gravis, motor neuron syndrome and thymoma

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dc.contributor.authorPandian, JD
dc.contributor.authorMathuranath, PS
dc.contributor.authorSuresh, PA
dc.contributor.authorRadhakrishnan, K
dc.date.accessioned2017-03-10T03:27:41Z
dc.date.available2017-03-10T03:27:41Z
dc.date.issued1998
dc.description.abstractAn adult male with thymomatous myasthenia gravis (MG) and a motor neuron syndrome simulating amyotrophic lateral sclerosis is reported. After thymectomy and corticosteroid therapy, the MG remitted. During 4 years of follow-up, the lower motor neuron signs in the upper limbs and upper motor neuron signs in the lower limbs remained unchanged. Literature concerning paraneoplastic neurological syndromes associated with thymoma has been reviewed.
dc.identifier.citation46 ,3;232-234en_US
dc.identifier.urihttps://dspace.sctimst.ac.in/handle/123456789/10099
dc.publisherNEUROLOGY INDIA
dc.subjectNeurosciences & Neurology
dc.titleMyasthenia gravis, motor neuron syndrome and thymoma
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