Author:
Kruijt N.,van den Bersselaar L.R.,Wijma J.,Verbeeck W.,Coenen M.J.H.,Neville J,Snoeck M.,Kamsteeg E.J.,Jungbluth H.,Kramers C.,Voermans N.C.
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference41 articles.
1. Rhabdomyolysis: pathogenesis, diagnosis, and treatment;Torres;Ochsner J,2015
2. Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis;Dlamini;Neuromuscul Disord,2013
3. The serotonin syndrome;Boyer;N Engl J Med,2005
4. Serotonin syndrome;Volpi-Abadie;Ochsner J,2013
5. The serotonin syndrome: from molecular mechanisms to clinical practice;Francescangeli;Int J Mol Sci,2019
Cited by
9 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