Rou-mu Hu
Beijing, 100020, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Hypocalcaemic cardiomyopathy with recurrent heart failure: a natural rechallenge case report with 30-month follow-up.
Journal: European heart journal. Case reports
Published: February 25, 2026
Expression defect of the rare variant/Brugada mutation R1512W depends upon the SCN5A splice variant background and can be rescued by mexiletine and the common polymorphism H558R.
Journal: Channels (Austin, Tex.)
Published: February 04, 2021
Investigation of the Cellular Pharmacological Mechanism and Clinical Evidence of the Multi-Herbal Antiarrhythmic Chinese Medicine Xin Su Ning.
Journal: Frontiers in pharmacology
Published: January 21, 2020
Study on the relationship between telomere length changes and recurrence of atrial fibrillation after radiofrequency catheter ablation.
Journal: Journal of cardiovascular electrophysiology
Published: December 13, 2018
Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients.
Journal: Channels (Austin, Tex.)
Published: July 10, 2018
Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends upon Splice Variant Background and Intracellular Acidosis.
Journal: PloS one
Published: January 21, 2015
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.
Journal: American journal of physiology. Heart and circulatory physiology
Published: February 05, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026