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

Year Number of Results
1999 1
2002 7
2003 2
2004 7
2005 5
2006 10
2007 10
2008 10
2009 12
2010 20
2011 11
2012 12
2013 23
2014 9
2015 26
2016 14
2017 18
2018 19
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2020 19
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2023 12
2024 2

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256 results

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Page 1
Ventricular non-compaction review.
Srivastava S, Yavari M, Al-Abcha A, Banga S, Abela G. Srivastava S, et al. Heart Fail Rev. 2022 Jul;27(4):1063-1076. doi: 10.1007/s10741-021-10128-3. Epub 2021 Jul 7. Heart Fail Rev. 2022. PMID: 34232438 Review.
Left ventricular non-compaction cardiomyopathy (LVNC) is a rare and unclassified cardiomyopathy that carries the potential to cause heart failure, arrhythmias, and embolic events within adults. ...Management of such cardiomyopathy has been debated in terms of
Left ventricular non-compaction cardiomyopathy (LVNC) is a rare and unclassified cardiomyopathy that carries the potential to
Cardiomyopathy: An Overview.
Brieler J, Breeden MA, Tucker J. Brieler J, et al. Am Fam Physician. 2017 Nov 15;96(10):640-646. Am Fam Physician. 2017. PMID: 29431384 Free article. Review.
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well as rare variants, such as arrhythmogenic right ventricular dysplasia and left ventricular noncompaction. In addit …
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well a …
Cardiomyopathy and pregnancy.
Schaufelberger M. Schaufelberger M. Heart. 2019 Oct;105(20):1543-1551. doi: 10.1136/heartjnl-2018-313476. Epub 2019 Jul 15. Heart. 2019. PMID: 31308064 Free PMC article. Review.
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ventricular, restrictive, Takotsubo and left ventricular non-compaction cardiomyopathies. ...However, patients with modest left ventric
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ventricular, restri …
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.
It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic dysfunction, or both, or various forms of congenital heart disease. Affected individuals are at risk of left or right ventricular failure, or both. Hear
It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic dysfunction, or both, or various for …
Excessive Trabeculation of the Left Ventricle: JACC: Cardiovascular Imaging Expert Panel Paper.
Petersen SE, Jensen B, Aung N, Friedrich MG, McMahon CJ, Mohiddin SA, Pignatelli RH, Ricci F, Anderson RH, Bluemke DA. Petersen SE, et al. JACC Cardiovasc Imaging. 2023 Mar;16(3):408-425. doi: 10.1016/j.jcmg.2022.12.026. Epub 2023 Feb 8. JACC Cardiovasc Imaging. 2023. PMID: 36764891 Free PMC article. Review.
Excessive trabeculation, often referred to as "noncompacted" myocardium, has been described at all ages, from the fetus to the adult. Current evidence for myocardial development, however, does not support the formation of compact myocardium from noncompacted myocard …
Excessive trabeculation, often referred to as "noncompacted" myocardium, has been described at all ages, from the fetus to the adult. …
Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.
Meyers DE, Basha HI, Koenig MK. Meyers DE, et al. Tex Heart Inst J. 2013;40(4):385-94. Tex Heart Inst J. 2013. PMID: 24082366 Free PMC article. Review.
Mitochondrial cardiomyopathy can be described as a myocardial condition characterized by abnormal heart-muscle structure, function, or both, secondary to genetic defects involving the mitochondrial respiratory chain, in the absence of concomitant coronary artery disease, h …
Mitochondrial cardiomyopathy can be described as a myocardial condition characterized by abnormal heart-muscle structure, function, o …
Differentiating Athlete's Heart From Cardiomyopathies - The Left Side.
Brosnan MJ, Rakhit D. Brosnan MJ, et al. Heart Lung Circ. 2018 Sep;27(9):1052-1062. doi: 10.1016/j.hlc.2018.04.297. Epub 2018 May 16. Heart Lung Circ. 2018. PMID: 29891249 Review.
In athletes who undertake a high volume of high intensity exercise, the resultant changes in cardiac structure and function which develop as a result of physiological adaptation to exercise (so called "Athlete's Heart") may overlap with some features of pathological condit …
In athletes who undertake a high volume of high intensity exercise, the resultant changes in cardiac structure and function which develop as …
Left ventricular noncompaction - Risk stratification and genetic consideration.
Ichida F. Ichida F. J Cardiol. 2020 Jan;75(1):1-9. doi: 10.1016/j.jjcc.2019.09.011. Epub 2019 Oct 17. J Cardiol. 2020. PMID: 31629663 Free article. Review.
Left ventricular noncompaction (LVNC) is a cardiomyopathy characterized by two layered structures composed of prominent trabecular meshwork and deep intertrabecular recesses. ...Clinical manifestations are highly variable, even in the same family, ranging fro
Left ventricular noncompaction (LVNC) is a cardiomyopathy characterized by two layered structures composed of prominent
Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors.
Finsterer J, Stöllberger C, Towbin JA. Finsterer J, et al. Nat Rev Cardiol. 2017 Apr;14(4):224-237. doi: 10.1038/nrcardio.2016.207. Epub 2017 Jan 12. Nat Rev Cardiol. 2017. PMID: 28079110 Review.
Left ventricular hypertrabeculation (LVHT) or noncompaction is a myocardial abnormality of unknown aetiology, frequently associated with monogenic disorders, particularly neuromuscular disorders, or with chromosomal defects. ...LVHT is categorized as distinct
Left ventricular hypertrabeculation (LVHT) or noncompaction is a myocardial abnormality of unknown aetiology, frequentl
Treatment Strategies for Cardiomyopathy in Children: A Scientific Statement From the American Heart Association.
Bogle C, Colan SD, Miyamoto SD, Choudhry S, Baez-Hernandez N, Brickler MM, Feingold B, Lal AK, Lee TM, Canter CE, Lipshultz SE; American Heart Association Young Hearts Pediatric Heart Failure and Transplantation Committee of the Council on Lifelong Congenital Heart Disease and Heart Health in the Young (Young Hearts). Bogle C, et al. Circulation. 2023 Jul 11;148(2):174-195. doi: 10.1161/CIR.0000000000001151. Epub 2023 Jun 8. Circulation. 2023. PMID: 37288568 Review.
This scientific statement from the American Heart Association focuses on treatment strategies and modalities for cardiomyopathy (heart muscle disease) in children and serves as a companion scientific statement for the recent statement on the classification and diagn …
This scientific statement from the American Heart Association focuses on treatment strategies and modalities for cardiomyopathy (h
256 results