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1993 1
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Page 1
Inherited cardiac arrhythmias.
Schwartz PJ, Ackerman MJ, Antzelevitch C, Bezzina CR, Borggrefe M, Cuneo BF, Wilde AAM. Schwartz PJ, et al. Nat Rev Dis Primers. 2020 Jul 16;6(1):58. doi: 10.1038/s41572-020-0188-7. Nat Rev Dis Primers. 2020. PMID: 32678103 Free PMC article. Review.
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia and Brugada syndrome. ...
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricul …
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 …
Pharmacology of Cenobamate: Mechanism of Action, Pharmacokinetics, Drug-Drug Interactions and Tolerability.
Roberti R, De Caro C, Iannone LF, Zaccara G, Lattanzi S, Russo E. Roberti R, et al. CNS Drugs. 2021 Jun;35(6):609-618. doi: 10.1007/s40263-021-00819-8. Epub 2021 May 16. CNS Drugs. 2021. PMID: 33993416 Review.
The most relevant safety issues are currently represented by the risk of severe skin reactions (apparently avoidable by a slow titration) and QT shortening (the drug is contraindicated in patients with familial short QT syndrome or taking QT-shortening drugs) …
The most relevant safety issues are currently represented by the risk of severe skin reactions (apparently avoidable by a slow titration) an …
CACNA1C-Related Disorders.
Napolitano C, Timothy KW, Bloise R, Priori SG. Napolitano C, et al. 2006 Feb 15 [updated 2021 Feb 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Feb 15 [updated 2021 Feb 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301577 Free Books & Documents. Review.
QT prolongation (QTc >480 ms) and arrhythmias in the absence of other syndromic features. Short QT syndrome (QTc <350 ms) or Brugada syndrome with short QT interval. ...
QT prolongation (QTc >480 ms) and arrhythmias in the absence of other syndromic features. Short QT syndrome (QTc &lt …
Short QT syndrome: The current evidences of diagnosis and management.
Dewi IP, Dharmadjati BB. Dewi IP, et al. J Arrhythm. 2020 Oct 6;36(6):962-966. doi: 10.1002/joa3.12439. eCollection 2020 Dec. J Arrhythm. 2020. PMID: 33335610 Free PMC article. Review.
There are many cardiac arrhythmias and sudden cardiac death (SCD) related to channelopathies or ion channel disorders. Short QT syndrome (SQTS) is an inherited cardiac channelopathy principally caused by defective functioning of both potassium-calcium ion cha …
There are many cardiac arrhythmias and sudden cardiac death (SCD) related to channelopathies or ion channel disorders. Short QT …
An Update on the Structure of hERG.
Butler A, Helliwell MV, Zhang Y, Hancox JC, Dempsey CE. Butler A, et al. Front Pharmacol. 2020 Jan 24;10:1572. doi: 10.3389/fphar.2019.01572. eCollection 2019. Front Pharmacol. 2020. PMID: 32038248 Free PMC article. Review.
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.
Pro-arrhythmic effects of gain-of-function potassium channel mutations in the short QT syndrome.
Hancox JC, Du CY, Butler A, Zhang Y, Dempsey CE, Harmer SC, Zhang H. Hancox JC, et al. Philos Trans R Soc Lond B Biol Sci. 2023 Jun 19;378(1879):20220165. doi: 10.1098/rstb.2022.0165. Epub 2023 May 1. Philos Trans R Soc Lond B Biol Sci. 2023. PMID: 37122211 Free PMC article. Review.
The congenital short QT syndrome (SQTS) is a rare condition characterized by abbreviated rate-corrected QT (QTc) intervals on the electrocardiogram and by increased susceptibility to both atrial and ventricular arrhythmias and sudden death. ...
The congenital short QT syndrome (SQTS) is a rare condition characterized by abbreviated rate-corrected QT (QTc) interv …
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.
39 results