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1963
2025

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

Year Number of Results
1963 4
1964 7
1966 4
1967 3
1968 7
1969 6
1970 10
1971 24
1972 19
1973 24
1974 24
1975 16
1976 20
1977 18
1978 11
1979 13
1980 15
1981 29
1982 11
1983 19
1984 28
1985 22
1986 21
1987 18
1988 39
1989 41
1990 42
1991 49
1992 55
1993 71
1994 55
1995 73
1996 80
1997 64
1998 59
1999 71
2000 88
2001 59
2002 84
2003 69
2004 68
2005 99
2006 96
2007 80
2008 81
2009 84
2010 102
2011 66
2012 83
2013 106
2014 92
2015 132
2016 100
2017 93
2018 85
2019 85
2020 78
2021 59
2022 61
2023 67
2024 57
2025 1

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2,947 results

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Page 1
Left ventricular non-compaction cardiomyopathy.
Towbin JA, Lorts A, Jefferies JL. Towbin JA, et al. Lancet. 2015 Aug 22;386(9995):813-25. doi: 10.1016/S0140-6736(14)61282-4. Epub 2015 Apr 9. Lancet. 2015. PMID: 25865865 Review.
Left ventricular non-compaction, the most recently classified form of cardiomyopathy, is characterised by abnormal trabeculations in the left ventricle, most frequently at the apex. It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic d …
Left ventricular non-compaction, the most recently classified form of cardiomyopathy, is characterised by abnormal trabeculations in …
CONGENITAL LONG QT SYNDROME: A SYSTEMATIC REVIEW.
Galić E, Bešlić P, Kilić P, Planinić Z, Pašalić A, Galić I, Ćubela VV, Pekić P. Galić E, et al. Acta Clin Croat. 2021 Dec;60(4):739-748. doi: 10.20471/acc.2021.60.04.22. Acta Clin Croat. 2021. PMID: 35734489 Free PMC article. Review.
Based on the results of a prospective study, it is suggested that the real prevalence of congenital LQTS is around 1:2000. Clinical manifestations of congenital LQTS include LQTS-attributable syncope, aborted cardiac arrest, and sudden cardiac death. Many patients w …
Based on the results of a prospective study, it is suggested that the real prevalence of congenital LQTS is around 1:2000. Clinical m …
Ventricular septal defect.
Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ. Spicer DE, et al. Orphanet J Rare Dis. 2014 Dec 19;9:144. doi: 10.1186/s13023-014-0144-2. Orphanet J Rare Dis. 2014. PMID: 25523232 Free PMC article. Review.
BACKGROUND: Ventricular septal defects are the commonest congenital cardiac malformations. They can exist in isolation, but are also found as integral components of other cardiac anomalies, such as tetralogy of Fallot, double outlet right ventricle, or common arterial trun …
BACKGROUND: Ventricular septal defects are the commonest congenital cardiac malformations. They can exist in isolation, but are also …
Diagnostic and prognostic role of electrocardiogram in acute myocarditis: A comprehensive review.
Buttà C, Zappia L, Laterra G, Roberto M. Buttà C, et al. Ann Noninvasive Electrocardiol. 2020 May;25(3):e12726. doi: 10.1111/anec.12726. Epub 2019 Nov 28. Ann Noninvasive Electrocardiol. 2020. PMID: 31778001 Free PMC article. Review.
In patients with myocarditis, electrocardiogram (ECG) can display a variety of non-specific abnormalities. Nevertheless, ECG is widely used as an initial screening tool for myocarditis. METHODS: We researched all possible ECG alterations during acute myocarditis evaluating …
In patients with myocarditis, electrocardiogram (ECG) can display a variety of non-specific abnormalities. Nevertheless, ECG is widel …
Pediatric arrhythmias.
Villain E. Villain E. Curr Opin Cardiol. 1994 Jan;9(1):114-20. doi: 10.1097/00001573-199401000-00014. Curr Opin Cardiol. 1994. PMID: 8199362 Review.
As children with cardiac malformations grow older, it appears that although their hemodynamic abnormalities may have been corrected by surgery, an increasing number of these patients have severe and possibly lethal arrhythmias. ...
As children with cardiac malformations grow older, it appears that although their hemodynamic abnormalities may have been corrected b …
Long-QT syndrome.
Kramer DB, Zimetbaum PJ. Kramer DB, et al. Cardiol Rev. 2011 Sep-Oct;19(5):217-25. doi: 10.1097/CRD.0b013e3182203504. Cardiol Rev. 2011. PMID: 21808164 Review.
Both categories are characterized by abnormally prolonged cardiac repolarization arising from a complex interaction between genetic and environmental factors. ...
Both categories are characterized by abnormally prolonged cardiac repolarization arising from a complex interaction between genetic a …
PACES/HRS expert consensus statement on the management of the asymptomatic young patient with a Wolff-Parkinson-White (WPW, ventricular preexcitation) electrocardiographic pattern: developed in partnership between the Pediatric and Congenital Electrophysiology Society (PACES) and the Heart Rhythm Society (HRS). Endorsed by the governing bodies of PACES, HRS, the American College of Cardiology Foundation (ACCF), the American Heart Association (AHA), the American Academy of Pediatrics (AAP), and the Canadian Heart Rhythm Society (CHRS).
Pediatric and Congenital Electrophysiology Society (PACES); Heart Rhythm Society (HRS); American College of Cardiology Foundation (ACCF); American Heart Association (AHA); American Academy of Pediatrics (AAP); Canadian Heart Rhythm Society (CHRS); Cohen MI, Triedman JK, Cannon BC, Davis AM, Drago F, Janousek J, Klein GJ, Law IH, Morady FJ, Paul T, Perry JC, Sanatani S, Tanel RE. Pediatric and Congenital Electrophysiology Society (PACES), et al. Heart Rhythm. 2012 Jun;9(6):1006-24. doi: 10.1016/j.hrthm.2012.03.050. Epub 2012 May 10. Heart Rhythm. 2012. PMID: 22579340 No abstract available.
2,947 results