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

Year Number of Results
1974 1
1975 1
1976 3
1977 5
1978 3
1979 1
1980 4
1981 4
1982 1
1983 6
1984 12
1985 15
1986 10
1987 22
1988 21
1989 31
1990 30
1991 24
1992 32
1993 32
1994 38
1995 32
1996 31
1997 42
1998 49
1999 35
2000 45
2001 54
2002 59
2003 71
2004 74
2005 95
2006 108
2007 126
2008 150
2009 177
2010 180
2011 209
2012 225
2013 252
2014 262
2015 253
2016 301
2017 320
2018 348
2019 348
2020 372
2021 388
2022 324
2023 276
2024 112

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4,868 results

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Page 1
Arrhythmogenic Cardiomyopathy.
Corrado D, Basso C, Judge DP. Corrado D, et al. Circ Res. 2017 Sep 15;121(7):784-802. doi: 10.1161/CIRCRESAHA.117.309345. Circ Res. 2017. PMID: 28912183 Review.
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. ...The main goal of treatment is the prevention of sudden cardiac death. Implantable c …
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly …
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.
Marian AJ, Braunwald E. Marian AJ, et al. Circ Res. 2017 Sep 15;121(7):749-770. doi: 10.1161/CIRCRESAHA.117.311059. Circ Res. 2017. PMID: 28912181 Free PMC article. Review.
In the majority of patients, HCM has a relatively benign course. However, HCM is also an important cause of sudden cardiac death, particularly in adolescents and young adults. Nonsustained ventricular tachycardia, syncope, a family history of sudden …
In the majority of patients, HCM has a relatively benign course. However, HCM is also an important cause of sudden cardiac …
2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: Executive Summary: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.
Ommen SR, Mital S, Burke MA, Day SM, Deswal A, Elliott P, Evanovich LL, Hung J, Joglar JA, Kantor P, Kimmelstiel C, Kittleson M, Link MS, Maron MS, Martinez MW, Miyake CY, Schaff HV, Semsarian C, Sorajja P. Ommen SR, et al. Circulation. 2020 Dec 22;142(25):e533-e557. doi: 10.1161/CIR.0000000000000938. Epub 2020 Nov 20. Circulation. 2020. PMID: 33215938 Free article. Review.
Brugada syndrome: Diagnosis, risk stratification and management.
Gourraud JB, Barc J, Thollet A, Le Marec H, Probst V. Gourraud JB, et al. Arch Cardiovasc Dis. 2017 Mar;110(3):188-195. doi: 10.1016/j.acvd.2016.09.009. Epub 2017 Jan 27. Arch Cardiovasc Dis. 2017. PMID: 28139454 Free article. Review.
Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of sudden cardiac death, despite a structurally normal heart. Diagnosis is based on a specific electrocardiogram pattern, observed either spontaneously or during a so …
Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of sudden cardiac death, despite …
Cardiac MRI to Predict Sudden Cardiac Death Risk in Dilated Cardiomyopathy.
Li Y, Xu Y, Li W, Guo J, Wan K, Wang J, Xu Z, Han Y, Sun J, Chen Y. Li Y, et al. Radiology. 2023 May;307(3):e222552. doi: 10.1148/radiol.222552. Epub 2023 Mar 14. Radiology. 2023. PMID: 36916890 Clinical Trial.
Background Sudden cardiac death (SCD) is one of the leading causes of death in individuals with nonischemic dilated cardiomyopathy (DCM). ...Conclusion Myocardial tissue characteristics derived from cardiac MRI were independent predictors of sudden …
Background Sudden cardiac death (SCD) is one of the leading causes of death in individuals with nonischemic dilated car …
2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines.
Ommen SR, Mital S, Burke MA, Day SM, Deswal A, Elliott P, Evanovich LL, Hung J, Joglar JA, Kantor P, Kimmelstiel C, Kittleson M, Link MS, Maron MS, Martinez MW, Miyake CY, Schaff HV, Semsarian C, Sorajja P. Ommen SR, et al. Circulation. 2020 Dec 22;142(25):e558-e631. doi: 10.1161/CIR.0000000000000937. Epub 2020 Nov 20. Circulation. 2020. PMID: 33215931 Free article. Review. No abstract available.
Brugada syndrome.
Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada P. Brugada R, et al. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):25-8. doi: 10.14797/mdcj-10-1-25. Methodist Debakey Cardiovasc J. 2014. PMID: 24932359 Free PMC article. Review.
It is associated with ventricular fibrillation and a high risk for sudden cardiac death, predominantly in younger males with structurally normal hearts. ...
It is associated with ventricular fibrillation and a high risk for sudden cardiac death, predominantly in younger males …
The Mitral Annular Disjunction of Mitral Valve Prolapse: Presentation and Outcome.
Essayagh B, Sabbag A, Antoine C, Benfari G, Batista R, Yang LT, Maalouf J, Thapa P, Asirvatham S, Michelena HI, Enriquez-Sarano M. Essayagh B, et al. JACC Cardiovasc Imaging. 2021 Nov;14(11):2073-2087. doi: 10.1016/j.jcmg.2021.04.029. Epub 2021 Jun 16. JACC Cardiovasc Imaging. 2021. PMID: 34147457 Free article.
During follow-up, 170 patients had clinical arrhythmic events (ventricular tachycardia, n = 159; arrhythmia ablation, n = 14; cardioverter-defibrillator implantation, n = 14; sudden cardiac death, n = 3). MAD was independently associated with higher risk for …
During follow-up, 170 patients had clinical arrhythmic events (ventricular tachycardia, n = 159; arrhythmia ablation, n = 14; cardioverter-d …
Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy.
Murphy SL, Anderson JH, Kapplinger JD, Kruisselbrink TM, Gersh BJ, Ommen SR, Ackerman MJ, Bos JM. Murphy SL, et al. J Cardiovasc Transl Res. 2016 Apr;9(2):153-61. doi: 10.1007/s12265-016-9681-5. Epub 2016 Feb 25. J Cardiovasc Transl Res. 2016. PMID: 26914223 Free PMC article.
This study set out to validate our recently developed phenotype-based HCM genotype predictor score. Patients clinically diagnosed with HCM and evaluated by genetic counselors comprised the study cohort. ...Cochran-Armitage analysis showed similar, statistically sign …
This study set out to validate our recently developed phenotype-based HCM genotype predictor score. Patients clinically diagno …
Clinical and genetic evaluation after sudden cardiac arrest.
Harris SL, Lubitz SA. Harris SL, et al. J Cardiovasc Electrophysiol. 2020 Feb;31(2):570-578. doi: 10.1111/jce.14333. Epub 2020 Jan 15. J Cardiovasc Electrophysiol. 2020. PMID: 31909521 Free PMC article. Review.
Sudden cardiac arrest (SCA) and sudden cardiac death (SCD) can be attributed to cardiac, respiratory, metabolic, and toxicologic etiologies. ...
Sudden cardiac arrest (SCA) and sudden cardiac death (SCD) can be attributed to cardiac, respiratory, metabolic, and to …
4,868 results