Paroxysmal extreme pain disorder: A very rare genetic aetiology of syncope with bizarre flushing in an infant-Reference-Cited by-同舟云学术

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Paroxysmal extreme pain disorder: A very rare genetic aetiology of syncope with bizarre flushing in an infant

Published:2020-09-12 Issue:6 Volume:57 Page:938-940
ISSN:1034-4810
Container-title:Journal of Paediatrics and Child Health
language:en
Short-container-title:J Paediatr Child Health

Author:

Bjeloševič Marko¹²^ORCID,Kušíková Katarína³,Tomko Jaroslav¹²,Illíková Viera²

Affiliation:

1. Department of Paediatric Cardiology, Faculty of Medicine Comenius University in Bratislava Bratislava Slovakia

2. Department of Arrhythmias and Cardiac Pacing Pediatric Cardiac Center, National Institute of Cardiovascular Diseases Bratislava Slovakia

3. Department of Paediatrics, Faculty of Medicine Comenius University in Bratislava Bratislava Slovakia

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpc.15072

Reference7 articles.

1. SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes

2. Paroxysmal Extreme Pain Disorder M1627K Mutation in Human Nav1.7 Renders DRG Neurons Hyperexcitable

3. Prolonged sinus pauses revealing a paroxysmal extreme pain disorder: Is it a frequent situation? A case report;Mouram S;Int. Arch. Med.,2015

4. Mutations in sodium channel gene SCN9A and the pain perception disorders;Marković D;Adv. Anesthesiol.,2015

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

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 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

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