Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1999 1
2004 1
2005 4
2006 3
2007 2
2008 1
2009 8
2010 4
2011 2
2012 7
2013 13
2014 9
2015 8
2016 6
2017 8
2018 6
2019 10
2020 11
2021 5
2022 4
2023 6
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

102 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Right ventricular noncompaction cardiomyopathy"
Page 1
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.
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical chest pain, heart failure, and sudden cardiac death. ...Family physicians should be alert for acquired variants of cardiomyopathy
Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can cause exertional dyspnea, presyncope, atypical c …
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. ...Complications include different …
The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy. Rare types are arrhythmogenic right ve
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. Heart f …
It can be associated with left ventricular dilation or hypertrophy, systolic or diastolic dysfunction, or both, or various forms of c …
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM 3rd, Hua W, Indik JH, Ingles J, James CA, John RM, Judge DP, Keegan R, Krahn AD, Link MS, Marcus FI, McLeod CJ, Mestroni L, Priori SG, Saffitz JE, Sanatani S, Shimizu W, van Tintelen JP, Wilde AAM, Zareba W. Towbin JA, et al. Heart Rhythm. 2019 Nov;16(11):e301-e372. doi: 10.1016/j.hrthm.2019.05.007. Epub 2019 May 9. Heart Rhythm. 2019. PMID: 31078652
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloidosis, sarcoidosis, Chagas disease, and left ventricular noncompaction. The ACM phenotype overlaps with other cardiomyopathi
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloid …
Pediatric Cardiomyopathies.
Lee TM, Hsu DT, Kantor P, Towbin JA, Ware SM, Colan SD, Chung WK, Jefferies JL, Rossano JW, Castleberry CD, Addonizio LJ, Lal AK, Lamour JM, Miller EM, Thrush PT, Czachor JD, Razoky H, Hill A, Lipshultz SE. Lee TM, et al. Circ Res. 2017 Sep 15;121(7):855-873. doi: 10.1161/CIRCRESAHA.116.309386. Circ Res. 2017. PMID: 28912187 Free PMC article. Review.
Pediatric cardiomyopathies are rare diseases with an annual incidence of 1.1 to 1.5 per 100 000. Dilated and hypertrophic cardiomyopathies are the most common; restrictive, noncompaction, and mixed cardiomyopathies occur infrequently; and arrhythmogeni …
Pediatric cardiomyopathies are rare diseases with an annual incidence of 1.1 to 1.5 per 100 000. Dilated and hypertrophic cardiomy
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G. Tsatsopoulou A, et al. Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3. Hellenic J Cardiol. 2023. PMID: 36870438 Free article. Review.
Paediatric cardiomyopathies form a heterogeneous group of disorders characterized by structural and electrical abnormalities of the heart muscle, commonly due to a gene variant of the myocardial cell structure. ...Arrhythmogenic right ventricular ca
Paediatric cardiomyopathies form a heterogeneous group of disorders characterized by structural and electrical abnormalities of the …
Cardiac MRI of Hereditary Cardiomyopathy.
Fadl SA, Revels JW, Rezai Gharai L, Hanneman K, Dana F, Proffitt EK, Grizzard JD. Fadl SA, et al. Radiographics. 2022 May-Jun;42(3):625-643. doi: 10.1148/rg.210147. Epub 2022 Mar 11. Radiographics. 2022. PMID: 35275782 Review.
T2*-weighted MRI is important in the detection and quantification of iron overload cardiomyopathy. Other hereditary entities for which comprehensive MRI has proven essential include Danon disease, familial dilated cardiomyopathy, hereditary muscular dystrophy, arrhy …
T2*-weighted MRI is important in the detection and quantification of iron overload cardiomyopathy. Other hereditary entities for whic …
The heart in m.3243A>G carriers.
Finsterer J, Zarrouk-Mahjoub S. Finsterer J, et al. Herz. 2020 Jun;45(4):356-361. doi: 10.1007/s00059-018-4739-6. Epub 2018 Aug 20. Herz. 2020. PMID: 30128910 Review. English.
Myocardial abnormalities include myocardial thickening, hypertrophic cardiomyopathy, dilated cardiomyopathy, noncompaction, myocardial fibrosis, systolic dysfunction, heart failure, or arterial hypertension. Arrhythmias reported in m.3243A>G carrier …
Myocardial abnormalities include myocardial thickening, hypertrophic cardiomyopathy, dilated cardiomyopathy, noncompaction
Hypertrabeculation; a phenotype with Heterogeneous etiology.
Adabifirouzjaei F, Igata S, DeMaria AN. Adabifirouzjaei F, et al. Prog Cardiovasc Dis. 2021 Sep-Oct;68:60-69. doi: 10.1016/j.pcad.2021.07.007. Epub 2021 Jul 13. Prog Cardiovasc Dis. 2021. PMID: 34265334 Free article. Review.
Left ventricular hypertrabeculation (LVHT) is a phenotype with multiple etiologies and variable clinical presentation and significance. ...However, due to the lack of consensus diagnostic criteria, LVHT has now been reported in a broad spectrum of cardiomyopathies, …
Left ventricular hypertrabeculation (LVHT) is a phenotype with multiple etiologies and variable clinical presentation and significanc …
Considerations for specific cardiomyopathies during pregnancy.
Abrams M, Magun E, DeFilippis EM. Abrams M, et al. Curr Opin Cardiol. 2023 May 1;38(3):233-240. doi: 10.1097/HCO.0000000000001033. Epub 2023 Mar 1. Curr Opin Cardiol. 2023. PMID: 37016994 Review.
The goal of this review is to summarize current knowledge on various cardiomyopathies in pregnancy, with an emphasis on cardiomyopathies beyond the most common in pregnancy, peripartum cardiomyopathy. ...Herein, we review and synthesize recent studies focusin …
The goal of this review is to summarize current knowledge on various cardiomyopathies in pregnancy, with an emphasis on cardiomyop
102 results