Associated Papers
Genetic and Clinical Insights into Inherited Erythromelalgia: A Comprehensive Review of Cases from China and Worldwide.
Li Y et al.
The Journal of Investigative Dermatology, 2026
Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.
Baker MD et al.
Pflugers Archiv : European Journal of Physiology, 2020
Q10R mutation in SCN9A gene is associated with generalized epilepsy with febrile seizures plus.
Cen Z et al.
Seizure, 2017
Short-lasting unilateral neuralgiform headache attacks with ispilateral facial flushing is a new variant of paroxysmal extreme pain disorder.
Imai N et al.
The Journal of Headache and Pain, 2015
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia.
Zhang Z et al.
Scandinavian Journal of Pain, 2014
Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.
Klein CJ et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2013
[Analysis of the families and the clinical phenotypes of the generalized epilepsy associated with adjunct febrile seizure].
Chen X et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2008
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