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Authors: Patrick L Sheets; James O Jackson; Stephen G Waxman; Sulayman D Dib-Hajj; Theodore R Cummins
Journal: J Physiol Date: 2007-04-12 Impact factor: 5.182

Review 5. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders.

Authors: Joost P H Drenth; Stephen G Waxman
Journal: J Clin Invest Date: 2007-12 Impact factor: 14.808

Review 6. Physiology and Pathophysiology of Itch.

Authors: Ferda Cevikbas; Ethan A Lerner
Journal: Physiol Rev Date: 2019-12-23 Impact factor: 37.312

7. A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia.

Authors: Tanya Z Fischer; Elaine S Gilmore; Mark Estacion; Emmanuella Eastman; Sean Taylor; Michel Melanson; Sulayman D Dib-Hajj; Stephen G Waxman
Journal: Ann Neurol Date: 2009-06 Impact factor: 10.422

8. E44Q mutation in Na_V1.7 in a patient with infantile paroxysmal knee pain: electrophysiological analysis of voltage-dependent sodium current.

Authors: Kiichi Takahashi; Takayoshi Ohba; Yosuke Okamoto; Atsuko Noguchi; Hiroko Okuda; Hatasu Kobayashi; Kouji H Harada; Akio Koizumi; Kyoichi Ono; Tsutomu Takahashi
Journal: Heliyon Date: 2021-06-24

9. Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labelling.

Authors: Andrew R Segerdahl; Jingyi Xie; Kathryn Paterson; Juan D Ramirez; Irene Tracey; David L H Bennett
Journal: Pain Date: 2012-02-24 Impact factor: 7.926

10. Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade.

Authors: Xiaoyang Cheng; Sulayman D Dib-Hajj; Lynda Tyrrell; Stephen G Waxman
Journal: Mol Pain Date: 2008-01-02 Impact factor: 3.395

Hereditary erythermalgia and acquired erythromelalgia.

1. Extending the clinical spectrum of pain channelopathies.

Review 2. Pain disorders and erythromelalgia caused by voltage-gated sodium channel mutations.

Review 3. Primary thrombocythemia: diagnosis, clinical manifestations and management.

4. A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity.