Andersen-Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat
Author:
Publisher
Oxford University Press (OUP)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
http://academic.oup.com/europace/article-pdf/15/12/1690/7279592/eut326.pdf
Reference14 articles.
1. Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations
2. Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation
3. Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
4. IK1 modulates the U-wave: insights in a 100-year-old enigma
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1. Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1;Nature Cardiovascular Research;2022-10-17
2. A peculiar case of palpitations and syncope;Heart Rhythm;2022-03
3. Catheter ablation of frequent monomorphic ventricular arrhythmias in Andersen-Tawil syndrome: case report and focused literature review;Journal of Interventional Cardiac Electrophysiology;2021-10-19
4. Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist;International Journal of Molecular Sciences;2021-08-27
5. Dual Dysfunction of Kir2.1 Underlies Conduction and Excitation-Contraction Coupling Defects Promoting Arrhythmias in a Mouse Model of Andersen-Tawil Syndrome Type 1;2021-06-17
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