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2018 1
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Page 1
Latent Causes of Sudden Cardiac Arrest.
Krahn AD, Tfelt-Hansen J, Tadros R, Steinberg C, Semsarian C, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Jun;8(6):806-821. doi: 10.1016/j.jacep.2021.12.014. JACC Clin Electrophysiol. 2022. PMID: 35738861 Free article. Review.
Less common and typically less apparent conditions that may not be readily evident include catecholaminergic polymorphic ventricular tachycardia, short QT syndrome and early repolarization syndrome. In cardiac arrest patients whose extensive testing does not …
Less common and typically less apparent conditions that may not be readily evident include catecholaminergic polymorphic ventricular tachyca …
"Short" also matters.
Lee CH, Scheinman MM. Lee CH, et al. Heart Rhythm. 2023 Aug;20(8):1197-1198. doi: 10.1016/j.hrthm.2023.02.026. Heart Rhythm. 2023. PMID: 37517862 No abstract available.
New drug discovery of cardiac anti-arrhythmic drugs: insights in animal models.
Sharma AK, Singh S, Bhat M, Gill K, Zaid M, Kumar S, Shakya A, Tantray J, Jose D, Gupta R, Yangzom T, Sharma RK, Sahu SK, Rathore G, Chandolia P, Singh M, Mishra A, Raj S, Gupta A, Agarwal M, Kifayat S, Gupta A, Gupta P, Vashist A, Vaibhav P, Kathuria N, Yadav V, Singh RP, Garg A. Sharma AK, et al. Sci Rep. 2023 Sep 29;13(1):16420. doi: 10.1038/s41598-023-41942-4. Sci Rep. 2023. PMID: 37775650 Free PMC article.
Genetic Arrhythmia: Channelopathies, Calcium Release Deficiency Syndrome, Long QT Syndrome, Short QT Syndrome, Brugada Syndrome. Genetic with Structural Heart Disease: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia, Dilated Cardiomyopathy, Hypertro …
Genetic Arrhythmia: Channelopathies, Calcium Release Deficiency Syndrome, Long QT Syndrome, Short QT Syndrome, Brugada …
Inherited Arrhythmia Syndromes.
Kim JA, Chelu MG. Kim JA, et al. Tex Heart Inst J. 2021 Sep 1;48(4):e207482. doi: 10.14503/THIJ-20-7482. Tex Heart Inst J. 2021. PMID: 34669951 Free PMC article. No abstract available.
Cardiac Repolarization in Health and Disease.
Krijger Juárez C, Amin AS, Offerhaus JA, Bezzina CR, Boukens BJ. Krijger Juárez C, et al. JACC Clin Electrophysiol. 2023 Jan;9(1):124-138. doi: 10.1016/j.jacep.2022.09.017. Epub 2022 Nov 30. JACC Clin Electrophysiol. 2023. PMID: 36697193 Free article. Review.
Atrial Fibrillation in Inherited Channelopathies.
Al-Azaam B, Darbar D. Al-Azaam B, et al. Card Electrophysiol Clin. 2021 Mar;13(1):155-163. doi: 10.1016/j.ccep.2020.10.004. Epub 2021 Jan 8. Card Electrophysiol Clin. 2021. PMID: 33516393 Free PMC article. Review.
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes.
Wu CI, Postema PG, Arbelo E, Behr ER, Bezzina CR, Napolitano C, Robyns T, Probst V, Schulze-Bahr E, Remme CA, Wilde AAM. Wu CI, et al. Heart Rhythm. 2020 Sep;17(9):1456-1462. doi: 10.1016/j.hrthm.2020.03.024. Epub 2020 Mar 31. Heart Rhythm. 2020. PMID: 32244059 Free PMC article. Review.
Management of patients with inherited arrhythmia syndromes such as long QT syndrome, Brugada syndrome, short QT syndrome, and catecholaminergic polymorphic ventricular tachycardia in the setting of the COVID-19 pandemic may prove particularly challenging. ...
Management of patients with inherited arrhythmia syndromes such as long QT syndrome, Brugada syndrome, short QT syndrome …
Preclinical short QT syndrome models: studying the phenotype and drug-screening.
Fan X, Yang G, Kowitz J, Duru F, Saguner AM, Akin I, Zhou X, El-Battrawy I. Fan X, et al. Europace. 2022 Mar 2;24(3):481-493. doi: 10.1093/europace/euab214. Europace. 2022. PMID: 34516623
Inherited cardiac channelopathies are linked to 5-10% of SCDs, mainly in the young. Short QT syndrome (SQTS) is a rare inherited channelopathy, which leads to both atrial and ventricular tachyarrhythmias, syncope, and even SCD. International European Society …
Inherited cardiac channelopathies are linked to 5-10% of SCDs, mainly in the young. Short QT syndrome (SQTS) is a rare …
59 results