Pediatric Erythromelalgia and SCN9A Mutations: Systematic Review and Single-Center Case Series-Reference-Cited by-同舟云学术

Pediatric Erythromelalgia and SCN9A Mutations: Systematic Review and Single-Center Case Series

Published:2019-03 Issue: Volume:206 Page:217-224.e9
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Arthur Luke^ORCID,Keen Kirsty,Verriotis Madeleine^ORCID,Peters Judy,Kelly Alison,Howard Richard F.,Dib-Hajj Sulayman D.,Waxman Stephen G.,Walker Suellen M.^ORCID

Funder

Great Ormond Street Hospital Children's Charity

Rehabilitation Research Service US Department of Veterans Affairs

The Erythromelalgia Association

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference109 articles.

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2. Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons;Dib-Hajj;Brain,2005

3. Erythromelalgia;Thompson;Clin Orthop Relat Res,1979

4. Natural history of erythromelalgia: presentation and outcome in 168 patients;Davis;Arch Dermatol,2000

5. Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy;Cummins;J Neurosci,2004

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1. Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7);Human Molecular Genetics;2023-09-18

2. Clinical Characterization of Pediatric Erythromelalgia: A Single-Center Case Series;Children;2023-07-26

3. Nav1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulation;Experimental Neurology;2023-06

4. Case report: Spinal cord stimulation in the treatment of pediatric erythromelalgia;Frontiers in Neurology;2023-05-18

5. A Review of the Therapeutic Targeting of SCN9A and Nav1.7 for Pain Relief in Current Human Clinical Trials;Journal of Pain Research;2023-05