Electrophysiological subtypes and prognosis of childhood Guillain–Barré syndrome in Japan
✍ Scribed by Kasumi Nagasawa; Satoshi Kuwabara; Sonoko Misawa; Katsunori Fujii; Yuzo Tanabe; Nobuhiro Yuki; Takamichi Hattori; Yoichi Kohno
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 83 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0148-639X
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Guillain-Barre ´syndrome (GBS) is recognized clinically by the presence of acute, rapidly progressive weakness, areflexia, and albuminocytological dissociation in cerebrospinal fluid. Although GBS was initially considered to be primarily an acute inflammatory demyelinating polyneuropathy (AIDP), sev
and the Plasma Exchange/Sandoglobulin Guillain-Bard Syndrome Trial Group7 We performed electrophysiological and serological testing within 15 days of symptom onset on 369 patients with Guillain-Bark Syndrome (GBS) enrolled in a trial comparing plasma exchange, intravenous immunoglobulin, and both t