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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1978 2
1979 1
1980 1
1982 1
1983 1
1984 3
1985 3
1986 5
1987 3
1988 1
1989 1
1990 6
1991 3
1992 3
1993 11
1994 9
1995 10
1996 7
1997 8
1998 12
1999 11
2000 16
2001 17
2002 34
2003 17
2004 21
2005 21
2006 19
2007 10
2008 17
2009 19
2010 25
2011 21
2012 21
2013 21
2014 20
2015 18
2016 18
2017 17
2018 13
2019 11
2020 16
2021 12
2022 17
2023 9
2024 6

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Search Results

499 results

Results by year

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Page 1
Ion Channel Diseases as a Cause of Sudden Cardiac Death in Young People: Aspects of Their Diagnosis, Treatment, and Pathogenesis.
El-Battrawy I, Mügge A, Akin I, Nguyen HP, Milting H, Aweimer A. El-Battrawy I, et al. Dtsch Arztebl Int. 2024 Oct 18;(Forthcoming):arztebl.m2024.0130. doi: 10.3238/arztebl.m2024.0130. Online ahead of print. Dtsch Arztebl Int. 2024. PMID: 38961815 Free article. Review.
The reported incidence figures for SCD vary widely. METHODS: This review is based on clinical registry studies, meta-analyses, randomized controlled trials, systematic reviews, and current guidelines that were retrieved by a selective search in PubMed employing the …
The reported incidence figures for SCD vary widely. METHODS: This review is based on clinical registry studies, meta-analyses, ran
Fetal Long QT Syndrome - Challenges in Perinatal Management: A Review and Case Report. Induction of Labor and Vaginal Birth Under Continuous Magnesium Therapy.
Wegner LS, Steinhard J, Frank T, Laser KT, Kubiak K. Wegner LS, et al. Z Geburtshilfe Neonatol. 2024 Feb 22. doi: 10.1055/a-2231-9348. Online ahead of print. Z Geburtshilfe Neonatol. 2024. PMID: 38387612 English.
Congenital LQTS is an often undetected inherited cardiac channel dysfunction and can be a reason for intrauterine fetal demise. ...Therefore, a thorough MEDLINE and Google Scholar search was conducted. Randomized controlled trials, meta-analyses, prospective and ret
Congenital LQTS is an often undetected inherited cardiac channel dysfunction and can be a reason for intrauterine fetal demise. ...Th
Relevance of mexiletine in the era of evolving antiarrhythmic therapy of ventricular arrhythmias.
Alhourani N, Wolfes J, Könemann H, Ellermann C, Frommeyer G, Güner F, Lange PS, Reinke F, Köbe J, Eckardt L. Alhourani N, et al. Clin Res Cardiol. 2024 Jun;113(6):791-800. doi: 10.1007/s00392-024-02383-9. Epub 2024 Feb 14. Clin Res Cardiol. 2024. PMID: 38353682 Free PMC article. Review.
., mainly amiodarone refractory ventricular arrhythmias, as well as those with selected forms of congenital long QT syndrome (LQTS) may nowadays still benefit from mexiletine. Here, we outline mexiletine's cellular and clinical electrophysiologi …
., mainly amiodarone refractory ventricular arrhythmias, as well as those with selected forms of congenital long QT
Repotrectinib in a Patient With NTRK Fusion-Positive Pancreatic Carcinoma and Congenital Long QT Syndrome.
Yun KM, Narezkina A, Redfern C, Velasco K, Bazhenova L. Yun KM, et al. JCO Precis Oncol. 2024 Jan;8:e2300265. doi: 10.1200/PO.23.00265. JCO Precis Oncol. 2024. PMID: 38271657
Repotrectinib in a patient with NTRK fusion-positive pancreatic carcinoma and congenital long QT syndrome....
Repotrectinib in a patient with NTRK fusion-positive pancreatic carcinoma and congenital long QT syndrome....
Effects of cohort, genotype, variant, and maternal beta-blocker treatment on foetal heart rate predictors of inherited long QT syndrome.
Kaizer AM, Winbo A, Clur SB, Etheridge SP, Ackerman MJ, Horigome H, Herberg U, Dagradi F, Spazzolini C, Killen SAS, Wacker-Gussmann A, Wilde AAM, Sinkovskaya E, Abuhamad A, Torchio M, Ng CA, Rydberg A, Schwartz PJ, Cuneo BF. Kaizer AM, et al. Europace. 2023 Nov 2;25(11):euad319. doi: 10.1093/europace/euad319. Europace. 2023. PMID: 37975542 Free PMC article.
AIMS: In long QT syndrome (LQTS), primary prevention improves outcome; thus, early identification is key. ...
AIMS: In long QT syndrome (LQTS), primary prevention improves outcome; thus, early identification is key. ...
Life-threatening cardiac arrhythmia and sudden death during electronic gaming: An international case series and systematic review.
Lawley CM, Tester M, Sanatani S, Prendiville T, Beach CM, Vinocur JM, Horie M, Uhm JS, Khongphatthanayothin A, Ayers MD, Starling L, Yoshida Y, Shah MJ, Skinner JR, Turner C. Lawley CM, et al. Heart Rhythm. 2022 Nov;19(11):1826-1833. doi: 10.1016/j.hrthm.2022.08.003. Epub 2022 Oct 11. Heart Rhythm. 2022. PMID: 37850595
Ten patients (45%) had catecholaminergic polymorphic ventricular tachycardia, 4 (18%) had long QT syndrome, 2 (9%) were post-congenital cardiac surgery, 2 (9%) had "idiopathic" ventricular fibrillation, and 1 (after Kawasaki disease) had coronary ische …
Ten patients (45%) had catecholaminergic polymorphic ventricular tachycardia, 4 (18%) had long QT syndrome, 2 (9%) were …
Association Between Syncope Trigger Type and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome.
Younis A, Bos JM, Zareba W, Aktas MK, Wilde AAM, Tabaja C, Bodurian C, Tobert KE, McNitt S, Polonsky B, Shimizu W, Ackerman MJ, Goldenberg I. Younis A, et al. JAMA Cardiol. 2023 Aug 1;8(8):775-783. doi: 10.1001/jamacardio.2023.1951. JAMA Cardiol. 2023. PMID: 37436769 Free PMC article.
IMPORTANCE: Syncope is the most powerful predictor for subsequent life-threatening events (LTEs) in patients with congenital long QT syndrome (LQTS). Whether distinct syncope triggers are associated with differential subsequent risk of LTEs is unknown. …
IMPORTANCE: Syncope is the most powerful predictor for subsequent life-threatening events (LTEs) in patients with congenital long
Prediction of Kv11.1 potassium channel PAS-domain variants trafficking via machine learning.
Immadisetty K, Fang X, Ramon GS, Hartle CM, McCoy TP, Center RG, Mirshahi T, Delisle BP, Kekenes-Huskey PM. Immadisetty K, et al. J Mol Cell Cardiol. 2023 Jul;180:69-83. doi: 10.1016/j.yjmcc.2023.05.002. Epub 2023 May 13. J Mol Cell Cardiol. 2023. PMID: 37187232
Congenital long QT syndrome (LQTS) is characterized by a prolonged QT-interval on an electrocardiogram (ECG). An abnormal prolongation in the QT-interval increases the risk for fatal arrhythmias. Genetic variants in several different card
Congenital long QT syndrome (LQTS) is characterized by a prolonged QT-interval on an electrocardiogram (E
Torsade de pointes secondary to long QT syndrome after intragastric balloon placement. A rare but severe complication.
García-Calonge M, González-Sánchez MH, Muíño-Domínguez D, Flórez-Díez P. García-Calonge M, et al. Rev Esp Enferm Dig. 2024 Mar;116(3):169-170. doi: 10.17235/reed.2023.9613/2023. Rev Esp Enferm Dig. 2024. PMID: 37114397 Free article.
During the patient's stay in the ED, two episodes of polymorphic ventricular tachychardia "Torsades de Pointes" (PVT-TDP) occurred, leading to cardiac arrest and requiring electrical cardioversion to restore sinus rhythm, in addition to a temporary pacemaker placement. Telemetry …
During the patient's stay in the ED, two episodes of polymorphic ventricular tachychardia "Torsades de Pointes" (PVT-TDP) occurred, leading …
Vandetanib.
Al-Ghusn AI, Bakheit AH, Attwa MW, AlRabiah H. Al-Ghusn AI, et al. Profiles Drug Subst Excip Relat Methodol. 2023;48:109-134. doi: 10.1016/bs.podrm.2022.11.004. Epub 2023 Feb 2. Profiles Drug Subst Excip Relat Methodol. 2023. PMID: 37061272 Review.
Because Vandetanib can make the Q-T interval last longer, it shouldn't be given to people with serious heart problems like congenital long QT syndrome or heart failure that hasn't been fixed yet. ...
Because Vandetanib can make the Q-T interval last longer, it shouldn't be given to people with serious heart problems like congenital
499 results