Inherited erythromelalgia due to mutations inSCN9A:natural history, clinical phenotype and somatosensory profile-Reference-Cited by-同舟云学术

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Inherited erythromelalgia due to mutations inSCN9A:natural history, clinical phenotype and somatosensory profile

Published:2016-02-26 Issue:4 Volume:139 Page:1052-1065
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

McDonnell Aoibhinn,Schulman Betsy,Ali Zahid,Dib-Hajj Sulayman D.,Brock Fiona,Cobain Sonia,Mainka Tina,Vollert Jan,Tarabar Sanela,Waxman Stephen G.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/139/4/1052/17348598/aww007.pdf

Reference53 articles.

1. Nav1.7 is the Predominant Sodium Channel in Rodent Olfactory Sensory Neurons

2. Value of quantitative sensory testing in neurological and pain disorders: NeuPSIG consensus

3. Depression and Pain Comorbidity

4. Painful and painless channelopathies

5. The validity of the Hospital Anxiety and Depression Scale

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