| Literature DB >> 11591857 |
C L Pan1, N Yuki, M Koga, M C Chiang, S T Hsieh.
Abstract
The authors describe two patients with acute sensory ataxic neuropathy. Both had a profound loss of proprioception and generalized areflexia. High titers of monospecific anti-GD1b IgG antibody were detected in their sera during the acute phase. Sensory ataxia resolved within 2 weeks after the onset. Taken together with the induction of experimental sensory ataxic neuropathy sensitized with GD1b ganglioside, GD1b may be a target molecule for autoantibody in some patients with acute sensory ataxic neuropathy.Entities:
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Year: 2001 PMID： 11591857 DOI： 10.1212/wnl.57.7.1316
Source DB: PubMed Journal: Neurology ISSN： 0028-3878 Impact factor: 9.910