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Xu, C. Guillain-Barré Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4065 (accessed on 27 September 2026).
Xu C. Guillain-Barré Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4065. Accessed September 27, 2026.
Xu, Camila. "Guillain-Barré Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4065 (accessed September 27, 2026).
Xu, C. (2020, December 23). Guillain-Barré Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4065
Xu, Camila. "Guillain-Barré Syndrome." Encyclopedia. Web. 23 December, 2020.
Guillain-Barré Syndrome
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/guillain-barre-syndrome

Guillain-Barré syndrome is an autoimmune disorder that affects the nerves.

genetic conditions

References

  1. Abraham LJ, Kroeger KM. Impact of the -308 TNF promoter polymorphism on thetranscriptional regulation of the TNF gene: relevance to disease. J Leukoc Biol. 1999 Oct;66(4):562-6. Review.
  2. Hughes RA, Cornblath DR. Guillain-Barré syndrome. Lancet. 2005 Nov5;366(9497):1653-66. Review.
  3. Ishikawa M, Kuroda Y, Kobayashi K, Sawada H, Hayashi M. Identification of abrain-specific 27/26-kDa extracellular protein with the monoclonal antibody todifferentiated PC12h pheochromocytoma cells. Exp Cell Res. 1991 Mar;193(1):151-4.
  4. Pithadia AB, Kakadia N. Guillain-Barré syndrome (GBS). Pharmacol Rep. 2010Mar-Apr;62(2):220-32. Review.
  5. Prasad KN, Nyati KK, Verma A, Rizwan A, Paliwal VK. Tumor necrosisfactor-alpha polymorphisms and expression in Guillain-Barré syndrome. HumImmunol. 2010 Sep;71(9):905-10. doi: 10.1016/j.humimm.2010.06.013.
  6. Zhang J, Dong H, Li B, Li CY, Guo L. Association of tumor necrosis factorpolymorphisms with Guillain-Barré syndrome. Eur Neurol. 2007;58(1):21-5.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 852
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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