Inhibition of Late Sodium Current by Mexiletine-Reference-Cited by-全球学者库

Inhibition of Late Sodium Current by Mexiletine

Published:2013-06 Issue:3 Volume:6 Page:614-622
ISSN:1941-3149
Container-title:Circulation: Arrhythmia and Electrophysiology
language:en
Short-container-title:Circ Arrhythm Electrophysiol

Author:

Gao Yuanfeng¹,Xue Xiaolin¹,Hu Dayi¹,Liu Wenling¹,Yuan Yue¹,Sun Hongmei¹,Li Lei¹,Timothy Katherine W.¹,Zhang Li¹,Li Cuilan¹,Yan Gan-Xin¹

Affiliation:

1. Heart Center, Peking University People’s Hospital, Beijing, People’s Republic of China (Y.G., D.H., W.L., L.L., C.L.); First Affiliated Hospital of Medical College of Xi’an Jiaotong University, Xi’an, People’s Republic of China (X.X., H.S., G.-X.Y.); Beijing Children’s Hospital, Capital University of Medical Sciences, Beijing, People’s Republic of China (Y.Y.); and Lankenau Medical Center, Lankenau Institute for Medical Research, Jefferson Medical College, Philadelphia, PA (K.W.T., L.Z., G.-X.Y.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference27 articles.

1. CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism

2. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

3. The Timothy syndrome mutation of cardiac CaV1.2 (L-type) channels: multiple altered gating mechanisms and pharmacological restoration of inactivation

4. Cellular basis for the electrocardiographic and arrhythmic manifestations of Timothy syndrome: Effects of ranolazine

5. Ranolazine Safely Decreases Ventricular and Atrial Fibrillation in Timothy Syndrome (LQT8)

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