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96 results

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Page 1
Catecholaminergic Polymorphic Ventricular Tachycardia.
Kim CW, Aronow WS, Dutta T, Frenkel D, Frishman WH. Kim CW, et al. Cardiol Rev. 2020 Nov/Dec;28(6):325-331. doi: 10.1097/CRD.0000000000000302. Cardiol Rev. 2020. PMID: 31934898 Review.
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare congenital arrhythmogenic disorder induced by physical or emotional stress. ...Mutations in the cardiac ryanodine receptor gene and the calsequestrin isoform 2 gene are most …
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare congenital arrhythmogenic disorder induce …
Calmodulin Mutations in Human Disease.
Hussey JW, Limpitikul WB, Dick IE. Hussey JW, et al. Channels (Austin). 2023 Dec;17(1):2165278. doi: 10.1080/19336950.2023.2165278. Channels (Austin). 2023. PMID: 36629534 Free PMC article. Review.
Calcium ions (Ca(2+)) are the basis of a unique and potent array of cellular responses. ...Mutations within any of these three genes may lead to severe cardiac deficits including severe long QT syndrome (LQTS) and/or catecholaminergic polymorphic ventricul …
Calcium ions (Ca(2+)) are the basis of a unique and potent array of cellular responses. ...Mutations within any of these three genes …
Advances in Cardiac Electrophysiology.
Piccini JP, Russo AM, Sharma PS, Kron J, Tzou W, Sauer W, Park DS, Birgersdotter-Green U, Frankel DS, Healey JS, Hummel J, Koruth J, Linz D, Mittal S, Nair DG, Nattel S, Noseworthy PA, Steinberg BA, Trayanova NA, Wan EY, Wissner E, Zeitler EP, Wang PJ. Piccini JP, et al. Circ Arrhythm Electrophysiol. 2022 Dec;15(12):e009911. doi: 10.1161/CIRCEP.121.009911. Epub 2022 Nov 28. Circ Arrhythm Electrophysiol. 2022. PMID: 36441565 Review.
Despite the global COVID-19 pandemic, during the past 2 years, there have been numerous advances in our understanding of arrhythmia mechanisms and diagnosis and in new therapies. ...There have been advances in our understanding of treatment of inherited disorders such as …
Despite the global COVID-19 pandemic, during the past 2 years, there have been numerous advances in our understanding of arrhythmia m …
[Syncopes and channelopathies].
Müller-Leisse J, Zormpas C, König T, Duncker D, Veltmann C. Müller-Leisse J, et al. Herzschrittmacherther Elektrophysiol. 2018 Jun;29(2):171-177. doi: 10.1007/s00399-018-0566-y. Epub 2018 May 15. Herzschrittmacherther Elektrophysiol. 2018. PMID: 29766267 Review. German.
Syncope can be the first manifestation of cardiac channelopathies, namely Brugada syndrome, long QT syndrome, short QT syndrome and catecholaminergic polymorphic ventricular tachycardia (CPVT). Patients affected by these rare diseases are at increased …
Syncope can be the first manifestation of cardiac channelopathies, namely Brugada syndrome, long QT syndrome, short QT syndrome and catec …
Catecholaminergic polymorphic ventricular tachycardia: a model for genotype-specific therapy.
Roston TM, Van Petegem F, Sanatani S. Roston TM, et al. Curr Opin Cardiol. 2017 Jan;32(1):78-85. doi: 10.1097/HCO.0000000000000360. Curr Opin Cardiol. 2017. PMID: 27861184 Review.
PURPOSE OF REVIEW: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a life-threatening syndrome defined by exercise-induced or emotion-induced ventricular arrhythmias, typically caused by gain-of-function mutations in RYR2-encoded ryanod …
PURPOSE OF REVIEW: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a life-threatening syndrome d …
Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist.
Kallas D, Lamba A, Roston TM, Arslanova A, Franciosi S, Tibbits GF, Sanatani S. Kallas D, et al. Int J Mol Sci. 2021 Aug 27;22(17):9293. doi: 10.3390/ijms22179293. Int J Mol Sci. 2021. PMID: 34502196 Free PMC article. Review.
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and potentially lethal inherited arrhythmia disease characterized by exercise or emotion-induced bidirectional or polymorphic ventricular tachyarrhythmias. ...The majority of CPVT p …
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and potentially lethal inherited arrhythm …
Calsequestrin. Structure, function, and evolution.
Wang Q, Michalak M. Wang Q, et al. Cell Calcium. 2020 Sep;90:102242. doi: 10.1016/j.ceca.2020.102242. Epub 2020 Jun 20. Cell Calcium. 2020. PMID: 32574906 Review.
Calsequestrin is the major Ca(2+) binding protein in the sarcoplasmic reticulum (SR), serves as the main Ca(2+) storage and buffering protein and is an important regulator of Ca(2+) release channels in both skeletal and cardiac muscle. ...Recent studies revea …
Calsequestrin is the major Ca(2+) binding protein in the sarcoplasmic reticulum (SR), serves as the main Ca(2+) storage and bu …
Risk stratification of sudden cardiac death: a review.
Tfelt-Hansen J, Garcia R, Albert C, Merino J, Krahn A, Marijon E, Basso C, Wilde AAM, Haugaa KH. Tfelt-Hansen J, et al. Europace. 2023 Aug 25;25(8):euad203. doi: 10.1093/europace/euad203. Europace. 2023. PMID: 37622576 Free PMC article. Review.
Treatment strategies include treatment of the underlying disease with lifestyle advice and drugs and decisions to implant a primary prevention implantable cardioverter-defibrillator (ICD) and perform ablation of the ventricles and novel treatment modalities such as left cardiac s …
Treatment strategies include treatment of the underlying disease with lifestyle advice and drugs and decisions to implant a primary preventi …
Ryanodine receptor channelopathies.
Betzenhauser MJ, Marks AR. Betzenhauser MJ, et al. Pflugers Arch. 2010 Jul;460(2):467-80. doi: 10.1007/s00424-010-0794-4. Epub 2010 Feb 24. Pflugers Arch. 2010. PMID: 20179962 Free PMC article. Review.
Over the past 20 years, numerous mutations in both RyR isoforms have been identified and linked to skeletal and cardiac diseases. Malignant hyperthermia, central core disease, and catecholaminergic polymorphic ventricular tachycardia have been genetica …
Over the past 20 years, numerous mutations in both RyR isoforms have been identified and linked to skeletal and cardiac diseases. Malignant …
Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.
Roston TM, Cunningham TC, Sanatani S. Roston TM, et al. Cardiol Young. 2017 Jan;27(S1):S49-S56. doi: 10.1017/S1047951116002237. Cardiol Young. 2017. PMID: 28084961 Review.
Since the sentinel description of exercise-triggered ventricular arrhythmias in 21 children, our recognition and understanding of catecholaminergic polymorphic ventricular tachycardia has improved substantially. ...Limited data have suggested that geno …
Since the sentinel description of exercise-triggered ventricular arrhythmias in 21 children, our recognition and understanding of catecho …
96 results