References
Fisher CM (1956) An unusual variant of acute idiopathic polyneuritis (syndrome of ophthalmoplegia, ataxia, areflexia). New Engl J Med 255:57–65
Frenzen P (2008) Economic cost of Guillain-Barré syndrome in the United States. Neurology 71:21–27
Godschalk PC, Heikema AP, Gilbert M, Komagamine T, Ang CW, Glerum J, Brochu D, Li J, Yuki N, Jacobs BC, van Belkum A, Endtz HP (2004) The crucial role of Campylobacter jejuni genes in anti-ganglioside antibody induction in Guillain-Barré syndrome. J Clin Invest 114:1659–1665
Goodyear CS, O’Hanlon GM, Plomp JJ, Wagner ER, Morrison I, Veitch J, Cochrane L, Bullens RW, Molenaar PC, Conner J, Willison HJ (1999) Monoclonal antibodies raised against Guillain-Barré syndrome-associated Campylobacter jejuni lipopolysaccharides react with neuronal gangliosides and paralyze muscle–nerve preparations. J Clin Invest 104:697–708
Guillain G, Barré JA, Strohl A (1916) Sur un syndrome de radiculonévrite avec hyperalbuminose du liquide céphalo-rachidien sans réaction cellulaire. Remarques sur les caractères cliniques et graphiques des réflexes tendineux. Bull Soc Méd Hôp Paris 40
Henderson R, Lawn N, Fletcher D, McClelland R, Wijdicks E (2003) The morbidity of Guillain-Barré syndrome admitted to the intensive care unit. Neurology 60:17–21
Ho TW, Mishu B, Li CY, Gao CY, Cornblath DR, Griffin JW, Asbury AK, Blaser MJ, McKhann GM (1995) Guillain-Barré syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies. Brain 118:597–605
Hughes RA, Cornblath DR (2005) Guillain-Barré syndrome. Lancet 366:1653–1666
Kieseier BC, Kiefer R, Gold R, Hemmer B, Willison HJ, Hartung HP (2004) Advances in understanding and treatment of immune-mediated disorders of the peripheral nervous system. Muscle Nerve 30:131–156
Lehmann HC, Kohne A, zu Horste GM, Kieseier BC (2007) Incidence of Guillain-Barré syndrome in Germany. J Peripher Nerv Syst 12:285
Lyu R, Chen S (2004) Acute multiple cranial neuropathy: a variant of Guillain-Barré syndrome? Muscle Nerve 30:433–436
McGrogan A, Madle G, Seaman H, de Vries C (2009) The epidemiology of Guillain-Barré syndrome worldwide. A systematic literature review. Neuroepidemiology 32:150–163
Ropper A (1994) Further regional variants of acute immune polyneuropathy. Bifacial weakness or sixth nerve paresis with paresthesias, lumbar polyradiculopathy, and ataxia with pharyngeal–cervical–brachial weakness. Arch Neurol 51:671–675
Susuki K, Koga M, Hirata K, Isogai E, Yuki N (2009) A Guillain-Barré syndrome variant with prominent facial diplegia. J Neurol (this issue)
Susuki K, Rasband MN, Tohyama K, Koibuchi K, Okamoto S, Funakoshi K, Hirata K, Baba H, Yuki N (2007) Anti-GM1 antibodies cause complement-mediated disruption of sodium channel clusters in peripheral motor nerve fibers. J Neurosci 27:3956–3967
Ter Bruggen J, van der Meché F, de Jager A, Polman C (1998) Ophthalmoplegic and lower cranial nerve variants merge into each other and into classical Guillain-Barré syndrome. Muscle Nerve 21:239–242
van Doorn PA, Ruts L, Jacobs BC (2008) Clinical features, pathogenesis, and treatment of Guillain-Barré syndrome. Lancet Neurol 7:939–950
Willison HJ, Yuki N (2002) Peripheral neuropathies and anti-glycolipid antibodies. Brain 125:2591–2625
Yuki N, Susuki K, Koga M, Nishimoto Y, Odaka M, Hirata K, Taguchi K, Miyatake T, Furukawa K, Kobata T, Yamada M (2004) Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barré syndrome. Proc Natl Acad Sci USA 101:11404–11409
Yuki N, Yamada M, Koga M, Odaka M, Susuki K, Tagawa Y, Ueda S, Kasama T, Ohnishi A, Hayashi S, Takahashi H, Kamijo M, Hirata K (2001) Animal model of axonal Guillain-Barré syndrome induced by sensitization with GM1 ganglioside. Ann Neurol 49:712–720
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Lehmann, H.C., Hartung, HP. Variants of Guillain-Barré syndrome: low incidence but high impact. J Neurol 256, 1909–1910 (2009). https://doi.org/10.1007/s00415-009-5253-9
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DOI: https://doi.org/10.1007/s00415-009-5253-9