Hereditary erythermalgia and acquired erythromelalgia - PubMed (original) (raw)

Comment

Hereditary erythermalgia and acquired erythromelalgia

P J van Genderen et al. Am J Med Genet. 1993.

No abstract available

PubMed Disclaimer

Comment on

• Autosomal dominant erythromelalgia.
  Finley WH, Lindsey JR Jr, Fine JD, Dixon GA, Burbank MK. Finley WH, et al. Am J Med Genet. 1992 Feb 1;42(3):310-5. doi: 10.1002/ajmg.1320420310. Am J Med Genet. 1992. PMID: 1536168

Similar articles

• [On the clinical features of erythromelalgia. Familial incidence of an idiopathic form in mother and daughter].
  Krebs A, Andres HU. Krebs A, et al. Schweiz Med Wochenschr. 1969 Mar 15;99(11):344-9. Schweiz Med Wochenschr. 1969. PMID: 5795636 German. No abstract available.
• Autosomal dominant erythromelalgia.
  Finley WH, Lindsey JR Jr, Fine JD, Dixon GA, Burbank MK. Finley WH, et al. Am J Med Genet. 1992 Feb 1;42(3):310-5. doi: 10.1002/ajmg.1320420310. Am J Med Genet. 1992. PMID: 1536168
• [Diagnosis of vascular acrosyndromes: essential acrocyanosis and erythermalgia].
  Lazareth I. Lazareth I. Agressologie. 1990 Apr;31(4):201-2. Agressologie. 1990. PMID: 2256537 French.
• [Classification of erythermalgia].
  Levesque H. Levesque H. J Mal Vasc. 1996;21(2):80-3. J Mal Vasc. 1996. PMID: 8755186 Review. French.
• [Erythermalgias].
  Lévesque H. Lévesque H. Rev Prat. 1998 Oct 1;48(15):1669-72. Rev Prat. 1998. PMID: 9814069 Review. French.

Cited by

• Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.
  Cummins TR, Dib-Hajj SD, Waxman SG. Cummins TR, et al. J Neurosci. 2004 Sep 22;24(38):8232-6. doi: 10.1523/JNEUROSCI.2695-04.2004. J Neurosci. 2004. PMID: 15385606 Free PMC article.
• Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labelling.
  Segerdahl AR, Xie J, Paterson K, Ramirez JD, Tracey I, Bennett DLH. Segerdahl AR, et al. Pain. 2012 May;153(5):1122-1127. doi: 10.1016/j.pain.2011.12.012. Epub 2012 Feb 24. Pain. 2012. PMID: 22365309 Free PMC article.
• A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity.
  Sheets PL, Jackson JO 2nd, Waxman SG, Dib-Hajj SD, Cummins TR. Sheets PL, et al. J Physiol. 2007 Jun 15;581(Pt 3):1019-31. doi: 10.1113/jphysiol.2006.127027. Epub 2007 Apr 12. J Physiol. 2007. PMID: 17430993 Free PMC article.
• Physiology and Pathophysiology of Itch.
  Cevikbas F, Lerner EA. Cevikbas F, et al. Physiol Rev. 2020 Jul 1;100(3):945-982. doi: 10.1152/physrev.00017.2019. Epub 2019 Dec 23. Physiol Rev. 2020. PMID: 31869278 Free PMC article. Review.
• Extending the clinical spectrum of pain channelopathies.
  Houlden H. Houlden H. Brain. 2012 Feb;135(Pt 2):313-6. doi: 10.1093/brain/aws007. Brain. 2012. PMID: 22345085 Free PMC article. No abstract available.

Publication types

MeSH terms

Substances

LinkOut - more resources

• Full Text Sources

  • Wiley