The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Long-Term Follow-Up of Patients With Short QT Syndrome
Open accessAbstract
Objectives The aim of this study was to investigate the clinical characteristics and the long-term course of a large cohort of patients with short QT syndrome (SQTS). Background SQTS is a rare channelopathy characterized by an increased risk of sudden death. Data on the long-term outcome of SQTS patients are not available. Methods Fifty-three patients from the European Short QT Registry (75% males; median age: 26 years) were followed up for 64 ± 27 months. Results A familial or personal history of cardiac arrest was present in 89%. Sudden death was the clinical presentation in 32%. The average QTc was 314 ± 23 ms. A mutation in genes related to SQTS was found in 23% of the probands; most of them had a gain of function mutation in HERG (SQTS1). Twenty-four patients received an implantable cardioverter defibrillator, and 12 patients received long-term prophylaxis with hydroquinidine (HQ), which was effective in preventing the induction of ventricular arrhythmias. Patients with a HERG mutation had shorter QTc at baseline and a greater QTc prolongation after treatment with HQ. During follow-up, 2 already symptomatic patients received appropriate implantable cardioverter defibrillator shocks and 1 had syncope. Nonsustained polymorphic ventricular tachycardia was recorded in 3 patients. The event rate was 4.9% per year in the patients without antiarrhythmic therapy. No arrhythmic events occurred in patients receiving HQ. Conclusions SQTS carries a high risk of sudden death in all age groups. Symptomatic patients have a high risk of recurrent arrhythmic events. HQ is effective in preventing ventricular tachyarrhythmia induction and arrhythmic events during long-term follow-up.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Quinidine therapy might provide some protection against VA; however, there are insufficient data to make any recommendations (305,306).”
From 2017 ACC/AHA/HRS Guideline for the Evaluation and Management of Patients With Syncope (2017) · cites this paper as [306]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Jervell, A., & Lange-Nielsen, F. (1957) · American Heart Journal · doi:10.1016/0002-8703(57)90079-0 · Cited by 1,601
Antzelevitch, C., Pollevick, G. D., Cordeiro, J. M., Casis, O., Sanguinetti, M. C., Aizawa, Y., Guerchicoff, A., Pfeiffer, R., Oliva, A., Wollnik, B., et al. (2007) · Circulation · doi:10.1161/circulationaha.106.668392 · Cited by 933 · cited 4×
“A family had a mutation in CACNB2b (8).”
InfluentialSelf-citationSudden death associated with short-QT syndrome linked to mutations in HERG
Brugada, R., Hong, K., Dumaine, R., Cordeiro, J., Gaita, F., Borggrefe, M., Menendez, T. M., Brugada, J., Pollevick, G. D., Wolpert, C., et al. (2004) · Circulation · doi:10.1161/01.cir.0000109482.92774.3a · Cited by 847
Self-citationShort QT Syndrome: A Familial Cause of Sudden Death
Gaita, F., Giustetto, C., Bianchi, F., Wolpert, C., Schimpf, R., Riccardi, R., Grossi, S., Richiardi, E., & Borggrefe, M. (2003) · Circulation · doi:10.1161/01.cir.0000085071.28695.c4 · Cited by 708
Self-citationIdiopathic Short QT Interval:A New Clinical Syndrome?
Gussak, I. B., Brugada, P., Brugada, J., Wright, R. S., Kopecky, S. L., CHAITMAN, B. R., & Bjerregaard, P. (2000) · Cardiology · doi:10.1159/000047299 · Cited by 669
Sex differences in the evolution of the electrocardiographic QT interval with age.
Rautaharju, P. M., Sh, Z., Wong, S., Hp, C., Berenson, G. S., Prineas, R., & Davignon, A. (1992) · PubMed · Cited by 635
A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene
Priori, S. G., Pandit, S. V., Rivolta, I., Berenfeld, O., Ronchetti, E., Dhamoon, A. S., Napolitano, C., ANUMONWO, J. M. B., di Barletta, M. R., Gudapakkam, S., et al. (2005) · Circulation Research · doi:10.1161/01.res.0000162101.76263.8c · Cited by 624
Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome
Bellocq, C., van Ginneken, A. C. G., Bezzina, C. R., Alders, M., Escande, D., Mannens, M. M. A. M., Baró, I., & Wilde, A. A. M. (2004) · Circulation · doi:10.1161/01.cir.0000130409.72142.fe · Cited by 614
Sauer, A. J., Moss, A. J., McNitt, S. A., Peterson, D. R., Zaręba, W., Robinson, J. L., Qi, M., Goldenberg, I., Hobbs, J. B., Ackerman, M. J., et al. (2007) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2006.08.057 · Cited by 417
Short QT syndrome: pharmacological treatment
Gaïta, F., Giustetto, C., Bianchi, F., Schimpf, R., Haı̈ssaguerre, M., Calò, L., Brugada, R., Antzelevitch, C. N., Borggrefe, M. M., & Wolpert, C. (2004) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.02.034 · Cited by 358
Self-citation
Cited by
Sorted by citations
Items 201–300 of 321
Inheritable Potassium Channel Diseases
Amin, A. S., & Wilde, A. A. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-44733-1.00052-3 · Cited by 4
Goldstein, S. A., Ward, C., & Al‐Khatib, S. M. (2017) · Journal of Innovations in Cardiac Rhythm Management · doi:10.19102/icrm.2018.090103 · Cited by 4
Horn, N., Rüb, N., & Wolpert, C. (2020) · Herzschrittmachertherapie + Elektrophysiologie · doi:10.1007/s00399-020-00666-y · Cited by 4
Electrophysiologic Study Indications And Evaluation
Majeed, H., & Sattar, Y. (2021) · StatPearls · Cited by 4
Schwartz, P. J., & Crotti, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-44733-1.00093-6 · Cited by 4
Plötzlicher Herztod junger Patienten
Schimpf, R., Yen, K., & Borggrefe, M. (2012) · Herzschrittmachertherapie + Elektrophysiologie · doi:10.1007/s00399-012-0228-4 · Cited by 4
Self-citationSudden Cardiac Death and Short QT Syndrome
Pavão, M. L. R. C., Ono, V. C., Arfelli, E., Simões, M. V., Marin‐Neto, J. A., & Schmidt, A. (2014) · Arquivos Brasileiros de Cardiologia · doi:10.5935/abc.20140133 · Cited by 4
Golovina, G., Duplyakov, D. V., & Dispensary, S. R. C. (2018) · Kardiologiia · doi:10.18087/cardio.2018.8.10151 · Cited by 4
Ventricular Arrhythmias in Inherited Channelopathies
Issa, Z. F., Miller, J. M., & Zipes, D. P. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4557-1274-8.00031-2 · Cited by 4
The Genetics of Cardiac Disease Associated with Sudden Cardiac Death
Perrin, M. J., & Gollob, M. H. (2012) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2012.04.002 · Cited by 4
Sun, H., Oh, Y., Ding, M., & Yang, P. C. (2015) · Pacing and Clinical Electrophysiology · doi:10.1111/pace.12659 · Cited by 4
Chen, Y., Ke, Y., Jiang, Z., & Yang, G. (2025) · Biomaterials Science · doi:10.1039/d5bm00194c · Cited by 5
Theory and practice of present clinical use of Quinidine in the management of cardiac arrhythmias
Belhassen, B., & Milman, A. (2025) · Indian Pacing and Electrophysiology Journal · doi:10.1016/j.ipej.2025.07.017 · Cited by 3
ICD-Therapie zur Primär- und Sekundärprophylaxe kongenitaler arrhythmogener Erkrankungen
Duncker, D., König, T., Hohmann, S., & Veltmann, C. (2015) · Herzschrittmachertherapie + Elektrophysiologie · doi:10.1007/s00399-015-0372-8 · Cited by 3
Medical Evaluation of Athletes: Genetic Testing
Gray, B. R., & Papadakis, M. (2020) · Springer eBooks · doi:10.1007/978-3-030-35374-2_11 · Cited by 3
Genome Editing and Myocardial Development
Turan, Ş., Chaillet, J. R., Stapleton, M. C., & Wu, Y. L. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-981-19-5642-3_4 · Cited by 3
Exercise in the Genetic Arrhythmia Syndromes - A Review.
Mareddy, C., ScM, M. T., McDaniel, G., & Monfredi, O. (2022) · Clinics in Sports Medicine · doi:10.1016/j.csm.2022.02.008 · Cited by 2
Updates on the Inherited Cardiac Ion Channelopathies: From Cell to Clinical
Silva, J. N. A., & Silva, J. R. (2012) · Current Treatment Options in Cardiovascular Medicine · doi:10.1007/s11936-012-0198-1 · Cited by 3
Schwartz, P. J., & Crotti, L. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4557-2856-5.00093-5 · Cited by 3
Inherited Arrhythmia Syndromes.
Kim, J. A., & Chelu, M. G. (2021) · PubMed Central · doi:10.14503/thij-20-7482 · Cited by 2
Exercise practice and short-QT interval on ECG
Mascia, G., Brugada, J., Arbelo, E., Minghini, A., Bianchi, L., Barca, L., Pierucci, N., Monaco, C., Donna, P. D., & Porto, I. (2025) · Journal of Electrocardiology · doi:10.1016/j.jelectrocard.2025.154173 · Cited by 2
Highlights of the Year in JACC 2011
DeMaria, A. N., Bax, J. J., Ben‐Yehuda, O., Feld, G. K., Greenberg, B., Hall, J., Hlatky, M. A., Lew, W. Y. W., Lima, J. A. C., Maisel, A. S., et al. (2012) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2011.12.013 · Cited by 2
Modelling of Genetic Cardiac Diseases
Prajapati, C., & Aalto‐Setälä, K. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.84965 · Cited by 2
Novedades en electrofisiología cardiaca y arritmias
Palmero, M. J. G., Alonso‐Martín, C., Font, E. R., & Viñolas, X. (2012) · Revista Española de Cardiología · doi:10.1016/j.recesp.2011.10.034 · Cited by 3
Human Genetics of Cardiac Arrhythmias
Schulze‐Bahr, E., & Dittmann, S. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-44087-8_66 · Cited by 2
Genetische Diagnostik zur Vermeidung des plötzlichen Herztods
Stallmeyer, B., Dittmann, S., & Schulze‐Bahr, E. (2018) · Der Internist · doi:10.1007/s00108-018-0462-x · Cited by 2
Hancox, J. C., Du, C., Zhang, H., Hancox, J. C., & Zhang, Y. (2020) · Journal of Integrative Cardiology Open Access · doi:10.31487/j.jicoa.2020.01.13 · Cited by 2
Primary ventricular fibrillation in a patient with mild hypercalcemia
Marinheiro, R., Parreira, L., Amador, P., Sardinha, F., Gonçalves, S., & Serra, S. (2018) · Arquivos Brasileiros de Cardiologia · doi:10.5935/abc.20180059 · Cited by 2
Synkopen und Ionenkanalerkrankungen
Müller‐Leisse, J., Zormpas, C., König, T., Duncker, D., & Veltmann, C. (2018) · Herzschrittmachertherapie + Elektrophysiologie · doi:10.1007/s00399-018-0566-y · Cited by 2
Specific Cardiovascular Diseases and Competitive Sports Participation: Channelopathies
Castelletti, S., & Crotti, L. (2020) · Springer eBooks · doi:10.1007/978-3-030-35374-2_20 · Cited by 1
Acquired (Drug-Induced) Long and Short QT Syndromes
Shah, R., & Gussak, I. (2013) · Springer eBooks · doi:10.1007/978-1-4471-4978-1_6 · Cited by 2
Bjerregaard, P., & Gussak, I. B. (2013) · Springer eBooks · doi:10.1007/978-1-4471-4881-4_33 · Cited by 2
Magnusson, P. O., & LeQuang, J. A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.89286 · Cited by 2
Abdulgader, A. A. A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.92073 · Cited by 1
A Review of JACC Articles on the Topic of Heart Rhythm Disorders: 2011–2012
Editors, T. (2013) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2013.09.026 · Cited by 2
Schimpf, R., & Borggrefe, M. M. (2011) · Heart Rhythm · doi:10.1016/j.hrthm.2011.08.006 · Cited by 2
Self-citationConsidering Ranolazine as a Potential Treatment for K+ Channel Linked Short QT Syndrome
Hancox, J. C. (2016) · Journal of Cardiovascular Electrophysiology · doi:10.1111/jce.13055 · Cited by 2
Implantable Devices in Genetic Heart Disease
Hansom, S. P., & Laksman, Z. (2023) · Cardiac Electrophysiology Clinics · doi:10.1016/j.ccep.2023.04.001 · Cited by 1
Kean, A. C., & Kannankeril, P. J. (2023) · Springer eBooks · doi:10.1007/978-3-030-42937-9_47-1 · Cited by 1
Soroush, N., Aarnoudse, A. L. H. J., Kavousi, M., Kors, J. A., Ikram, M. A., Stricker, B. H. C., & Ahmadizar, F. (2024) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.16130 · Cited by 1
Risk Stratification in the Short-QT Syndrome: Findings From a Pooled Analysis.
Giladi, M., Solomon, A., Viskin, D., Rosso, R., van der Werf, C., Pinto, S. G., Wilde, A., Elbassel, R., Henriques, L., Bos, J., et al. (2026) · Heart Rhythm · doi:10.1016/j.hrthm.2026.03.001 · Cited by 1
Bidzimou, M.-T. K., Muralidharan, P., Zhang, Z., Raza, D. S., Needs, D., Sun, B., Perelli, R. M., Moya‐Mendez, M. E., Manivannan, P. K. R., Hunanyan, A. S., et al. (2026) · JCI Insight · doi:10.1172/jci.insight.197721 · Cited by 1
97 – Idiopathic Ventricular Fibrillation
Veltmann, C., Schimpf, R., & Borggrefe, M. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-2856-5.00097-2 · Cited by 1
Self-citationShort QT syndrome presenting as syncope: How short is too short?
Portugal, G., Oliveira, M., Cunha, P. S., Ferreira, F., Lousinha, A., Fiarresga, A. J., da Silva, M. N., & Ferreira, F. (2014) · Revista Portuguesa de Cardiologia (English Edition) · doi:10.1016/j.repce.2014.05.002 · Cited by 1
Precision medicine in cardiac electrophysiology: where we are and where we need to go
Correa, A. A., Haider, S. W., & Aronow, W. S. (2020) · Expert Review of Precision Medicine and Drug Development · doi:10.1080/23808993.2020.1754127 · Cited by 1
Genetics of Cardiovascular Disease and Applications of Genetic Testing
Mahdieh, N., Rabbani, B., & Maleki, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-80915-3.00025-9 · Cited by 1
Venetucci, L. A., & Garratt, C. J. (2014) · Medicine · doi:10.1016/j.mpmed.2014.07.014 · Cited by 1
Lee, C., & Scheinman, M. M. (2023) · Heart Rhythm · doi:10.1016/j.hrthm.2023.02.026 · Cited by 1
Inherited Arrhythmias: LQTS/SQTS/CPVT
Mazzanti, A., & Priori, S. (2018) · Springer eBooks · doi:10.1007/978-3-319-66114-8_13 · Cited by 1
Self-citationZaręba, W., & Platonov, P. G. (2018) · doi:10.1093/med/9780198784906.003.0074 · Cited by 1
2018 KHRS Guidelines for Catheter Ablation of Ventricular Arrhythmias – Part1
Roh, S., Kim, S., Kim, Y.-N., Kim, J.-Y., Kim, J., Kim, T., Nam, G., Park, K., Park, H., Pak, H., et al. (2018) · International Journal of Arrhythmia · doi:10.18501/arrhythmia.2018.006 · Cited by 1
Suzuki, H. (2019) · Japanese Society of Pediatric Cardiology and Cardiac Surgery · doi:10.9794/jspccs.35.249 · Cited by 1
Abdulgader, A. A. A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.92131 · Cited by 1
Fowler, S. J., Chinitz, L. A., & Priori, S. G. (2012) · doi:10.1002/9781118481585.ch59 · Cited by 1
Tülümen, E., Giustetto, C., Wolpert, C., Maury, P., Anttonen, O. M., Probst, V., Blanc, J., Sbragia, P., Scrocco, C., Rudic, B., et al. (2014) · Heart Rhythm · doi:10.1016/j.hrthm.2014.04.028 · Cited by 1
Self-citationCould ivabradine be a new treatment for the short QT syndrome?
Hancox, J. C. (2017) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12802 · Cited by 1
Ventricular tachycardia and ventricular fibrillation
(2013) · Wiley eBooks · doi:10.1002/9781118521991.ch7 · Cited by 1
Adler, A., & Gollob, M. H. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809657-4.99760-6 · Cited by 1
Srour, M. K., Bidzimou, M.-T. K., Muralidharan, P., Mitchell, S. M., Moya‐Mendez, M. E., Parker, L. E., Valenzuela, G. R., Caraballo, R. H., Garone, G., Vigevano, F., et al. (2024) · medRxiv · doi:10.1101/2024.08.31.24312446 · Cited by 2
Schimpf, R., & Borggrefe, M. (2015) · Springer eBooks · doi:10.1007/978-3-642-54676-1_178-1
Self-citationClinical Role of Antiarrhythmic Drugs in the Prevention of Sudden Death
Lee, H.-C., & Huang, K. T. L. (2013) · Springer eBooks · doi:10.1007/978-1-4471-4978-1_33
Electrocardiographic Characteristics of Ventricular Arrhythmia in Inherited Channelopathies
Methachittiphan, N., Deeprasertkul, P., & Link, M. (2014) · Cardiac Electrophysiology Clinics · doi:10.1016/j.ccep.2014.05.013
Does a Short QT Interval Presage a Short Life Span
Manolis, A. S., Koulouris, S. N., & Kappos, K. G. (2012) · Hospital chronicles/Hospital Chronicles · doi:10.2015/hc.v7i4.529
Cardiovascular screening in young athletes: controversies and feasibility
(2013) · Cardiovascular Medicine · doi:10.4414/cvm.2013.00101
Antiarrhythmic Drugs and Management of Ventricular Arrhythmias
Schleifer, J. W., & Srivathsan, K. S. (2015) · Springer eBooks · doi:10.1007/978-3-319-15961-4_52
Genetic Arrhythmias (Channelopathies)
Mazzanti, A., Ng, K. K., & Priori, S. G. (2015) · KARGER eBooks · doi:10.1159/000375217
Self-citationAcute Management of Arrhythmias in Patients with Channelopathies
Bianchi, F., & Grossi, S. (2015) · Springer eBooks · doi:10.1007/978-3-319-24328-3_8
The Genetics of Cardiac Disease Associated with
Perrin, M. J., & Gollob, M. H. (2012)
Tsuji, Y., Harrell, D. T., Ishikawa, T., & Makita, N. (2015) · Japanese Journal of Electrocardiology · doi:10.5105/jse.35.104
Sudden Cardiac Death in Athletes: Current Knowledge and Newer Concepts
Lévy, S. (2015) · Journal of Heart Health · doi:10.16966/2379-769x.111
Parakh, N. (2015) · Journal of the Practice of Cardiovascular Sciences · doi:10.4103/2395-5414.166320
Crotti, L., Kotta, M., & Castelletti, S. (2018) · Cardiac and vascular biology · doi:10.1007/978-3-319-77812-9_7
Atrial Fibrillation: Epidemiology and Demographics
Soto‐Ruiz, K. M. (2016) · Contemporary cardiology · doi:10.1007/978-3-319-31386-3_1
Implantable Cardioverter-Defibrillators in Inherited Arrhythmia Syndromes
Nordkamp, L. R. A. O., & Wilde, A. A. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-37804-8.00021-3
Cardiac channelopathies – A too frequently trivialized problem?
Urbańczuk, M., & Jaroszyński, A. (2015) · Journal of Pre-Clinical and Clinical Research · doi:10.5604/18982395.1157580
Modelling the Effects of Disopyramide on Short QT Syndrome Variant 1 in the Human Ventricles
Whittaker, D. J., Ni, H., Benson, A. P., Hancox, J. C., & Zhang, H. (2016) · Computing in cardiology · doi:10.22489/cinc.2016.003-435
Gollob, M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99760-5 · Cited by 1
Clinical Management of Inherited Arrhythmias
Jones, R., & Perez, M. V. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99829-5
Matassini, M. V., & Maolo, A. (2015) · Springer eBooks · doi:10.1007/978-3-319-19926-9_25
Inherited Conduction Disease and Atrial Fibrillation
Martin, C., & Lambiase, P. D. (2018) · Springer eBooks · doi:10.1007/978-3-319-66114-8_15
Genetic Testing for Inheritable Cardiac Channelopathies
Kyndt, F., Gourraud, J., & Barc, J. (2018) · Cardiac and vascular biology · doi:10.1007/978-3-319-77812-9_13
Channellopathies: New ECG Criteria for Risk Stratification
Compagnucci, P., D'Agostino, S., Quaranta, A., & Spinucci, G. (2018) · New Concepts in ECG Interpretation · doi:10.1007/978-3-319-91677-4_12
Mahdieh, N., & Maleki, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-51149-0.00030-4
Electrocardiograms Associated with Sudden Cardiac Death
Borggrefe, M. (2019) · European Journal of Arrhythmia & Electrophysiology · doi:10.17925/ejae.2019.5.1.13
Self-citationShort QT Interval and Short QT Syndrome
Suzuki, H. (2019) · Japanese Society of Pediatric Cardiology and Cardiac Surgery · doi:10.9794/jspccs.35.9
Neuromodulation of Cardiac Repolarization and Arrhythmogenesis
Extramiana, F., & Maison‐Blanche, P. (2019) · Springer eBooks · doi:10.1007/978-3-030-22672-5_2
Scrocco, C., Gaita, F., & Giustetto, C. (2019) · Cardiac Repolarization · doi:10.1007/978-3-030-22672-5_18 · Cited by 32
Self-citationRare but lethal short QT syndrome: most recent understanding of the disease
Rico-Mesa, J. S., Qaysi, M. A., Sovic, W., Endo-Carvajal, M., & Badin, A. (2019) · Electronic Journal of General Medicine · doi:10.29333/ejgm/108495
Inheritable Potassium Channel Disease
Al‐Ahmad, A., & Wilde, A. A. M. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4557-2856-5.00051-0
The Channelopathies and Sudden Death
Gomes, J. (2020) · Springer eBooks · doi:10.1007/978-3-030-45066-3_19
Long-term Prognosis of Short QT Interval in Asian Patients: Multicenter Retrospective Cohort StudyPreprint
Kim, D. Y., Uhm, J., Kim, M. H., Kim, I. S., Jin, M., Yu, H. T., Kim, T. H., Kim, J., Joung, B., Pak, H., et al. (2020) · doi:10.22541/au.159969682.20226591
Nikoo, M., Heiran, A., Mashayekh, F., Rezaianzadeh, A., Shiravani, A., & Azadian, F. (2021) · Research Square · doi:10.21203/rs.3.rs-579266/v1
Evaluation and care of common pediatric cardiac disorders
Wood, K. P., Sooy-Mossey, M., & Campbell, M. J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818872-9.00055-8
Genetics of Sudden Cardiac Death, the Channelopathies: Today's Perspective and the Future
Alabdulgader, A. (2021) · Cardiology & Vascular Research · doi:10.33425/2639-8486.1115
Gencher, J. A., Deif, B., & Roberts, J. D. (2020) · Springer eBooks · doi:10.1007/978-3-030-52173-8_3
Wolpert, C., & Rüb, N. (2016) · Springer eBooks · doi:10.1007/978-3-319-44203-7_13
Clinical Management of Inherited Arrhythmias
Jones, R. L., & Perez, M. V. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809657-4.99829-6
Wolpert, C., & Schulze‐Bahr, E. (2020) · Springer eBooks · doi:10.1007/978-3-030-45457-9_13
Antzelevitch, C. N. (2020) · Contemporary cardiology · doi:10.1007/978-3-030-41967-7_34
Adeniran, I. (2014) · Springer theses · doi:10.1007/978-3-319-07200-5_3
Metadata
- Authors
- Giustetto, C., Schimpf, R., Mazzanti, A., Scrocco, C., Maury, P., Anttonen, O., Probst, V., Blanc, J.-J., Sbragia, P., Dalmasso, P., Borggrefe, M., & Gaita, F.
- Affiliations
- Azienda Ospedaliero Universitaria San Giovanni Battista (IT)
- University Medical Centre Mannheim (DE)
- Hôpital Rangueil (FR)
- Päijät-Hämeen Keskussairaala (FI)
- Institut du Thorax (FR)
- Université de Bretagne Occidentale (FR)
- Hôpital Nord (FR)
- University of Turin (IT)
- Corresponding author
- Giustetto, Carla
- ORCID
- Venue
- Journal of the American College of Cardiology
- Publisher
- Elsevier BV
- Published
- 2011-08
- Volume
- 58
- Issue
- 6
- Pages
- 587-595
- ISSN
- 0735-1097 (ISSN-L)
- OpenAlex
- W2006047900
- Cited by
- 325
- References
- 25
- Citations by year
- 2026: 10 · 2025: 11 · 2024: 20 · 2023: 14 · 2022: 14 · 2021: 17 · 2020: 26 · 2019: 21 · 2018: 26 · 2017: 32 · 2016: 16 · 2015: 33 · 2014: 21 · 2013: 31 · 2012: 28
- FWCI
- 18.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of the American College of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion, other-oa)
- Funders
- Foundation Cassa di Risparmio of Asti
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Effects of Exercise
- Keywords
- short QT syndrome, sudden cardiac death, sudden cardiac arrest, gain-of-function mutations, QTc prolongation, hydroquinidine, implantable cardioverter-defibrillator, ventricular tachyarrhythmia, long-term follow-up, channelopathies, antiarrhythmic prophylaxis
- MeSH terms
- ERG1 Potassium Channel, Adolescent, Adult, Anti-Arrhythmia Agents, Arrhythmias, Cardiac, Death, Sudden, Electrocardiography, Female, Follow-Up Studies, Humans, Male, Middle Aged, Mutation, Quinidine, Syncope, Cohort Studies, Treatment Outcome, Defibrillators, Implantable, Ether-A-Go-Go Potassium Channels
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review