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Year Number of Results
1950 4
1952 1
1954 1
1956 1
1959 1
1960 1
1961 4
1962 5
1963 1
1964 2
1965 1
1969 1
1970 7
1971 9
1972 6
1973 7
1974 6
1975 18
1976 8
1977 22
1978 15
1979 8
1980 22
1981 27
1982 48
1983 122
1984 251
1985 300
1986 330
1987 334
1988 368
1989 433
1990 474
1991 501
1992 479
1993 442
1994 411
1995 482
1996 440
1997 471
1998 482
1999 557
2000 615
2001 567
2002 589
2003 605
2004 591
2005 743
2006 741
2007 745
2008 784
2009 781
2010 787
2011 738
2012 779
2013 818
2014 718
2015 766
2016 783
2017 742
2018 735
2019 717
2020 752
2021 784
2022 732
2023 648
2024 291

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22,657 results

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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.
Cardiomyopathy can be separated into primary (genetic, mixed, or acquired) and secondary categories, which result in varied phenotypes including dilated, hypertrophic, and restrictive patterns. Hypertrophic cardiomyopathy is the most common primary cardiomyopathy and can c …
Cardiomyopathy can be separated into primary (genetic, mixed, or acquired) and secondary categories, which result in varied phenotypes inclu …
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.
Cardiomyopathy is a group of disorders in which the heart muscle is structurally and functionally abnormal in the absence of other diseases that could cause observed myocardial abnormality. The most common cardiomyopathies are hypertrophic and dilated cardiomyopathy …
Cardiomyopathy is a group of disorders in which the heart muscle is structurally and functionally abnormal in the absence of other diseases …
Cardiomyopathies: An Overview.
Ciarambino T, Menna G, Sansone G, Giordano M. Ciarambino T, et al. Int J Mol Sci. 2021 Jul 19;22(14):7722. doi: 10.3390/ijms22147722. Int J Mol Sci. 2021. PMID: 34299342 Free PMC article. Review.
BACKGROUND: Cardiomyopathies are a heterogeneous group of pathologies characterized by structural and functional alterations of the heart. ...The search keywords were "cardiomyopathies, sudden cardiac arrest, dilated cardiomyopathy (DCM), hypertrophic cardiom …
BACKGROUND: Cardiomyopathies are a heterogeneous group of pathologies characterized by structural and functional alterations of the h …
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.
Pinto YM, Elliott PM, Arbustini E, Adler Y, Anastasakis A, Böhm M, Duboc D, Gimeno J, de Groote P, Imazio M, Heymans S, Klingel K, Komajda M, Limongelli G, Linhart A, Mogensen J, Moon J, Pieper PG, Seferovic PM, Schueler S, Zamorano JL, Caforio AL, Charron P. Pinto YM, et al. Eur Heart J. 2016 Jun 14;37(23):1850-8. doi: 10.1093/eurheartj/ehv727. Epub 2016 Jan 19. Eur Heart J. 2016. PMID: 26792875 Review.
In this paper the Working Group on Myocardial and Pericardial Disease proposes a revised definition of dilated cardiomyopathy (DCM) in an attempt to bridge the gap between our recent understanding of the disease spectrum and its clinical presentation in relatives, which is …
In this paper the Working Group on Myocardial and Pericardial Disease proposes a revised definition of dilated cardiomyopathy (DCM) i …
Neonatal dilated cardiomyopathy.
Soares P, Rocha G, Pissarra S, Soares H, Flôr-de-Lima F, Costa S, Moura C, Dória S, Guimarães H. Soares P, et al. Rev Port Cardiol. 2017 Mar;36(3):201-214. doi: 10.1016/j.repc.2016.10.007. Epub 2017 Feb 28. Rev Port Cardiol. 2017. PMID: 28256370 Free article. Review. English, Portuguese.
Dilated cardiomyopathy is the commonest cardiomyopathy in children, and the majority present before one year of age. ...Marked dilatation of the left ventricle with global hypokinesis is the hallmark of the disease. ...
Dilated cardiomyopathy is the commonest cardiomyopathy in children, and the majority present before one year of age. ...Marked dil …
Epidemiology of the inherited cardiomyopathies.
McKenna WJ, Judge DP. McKenna WJ, et al. Nat Rev Cardiol. 2021 Jan;18(1):22-36. doi: 10.1038/s41569-020-0428-2. Epub 2020 Sep 7. Nat Rev Cardiol. 2021. PMID: 32895535 Review.
The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic right ventricular cardiomyopathy (1/5,000) are probably conservative given that only individuals who fulfil diagnostic criteria would have been inclu …
The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic right ven …
Arrhythmias as Presentation of Genetic Cardiomyopathy.
Lukas Laws J, Lancaster MC, Ben Shoemaker M, Stevenson WG, Hung RR, Wells Q, Marshall Brinkley D, Hughes S, Anderson K, Roden D, Stevenson LW. Lukas Laws J, et al. Circ Res. 2022 May 27;130(11):1698-1722. doi: 10.1161/CIRCRESAHA.122.319835. Epub 2022 May 26. Circ Res. 2022. PMID: 35617362 Free PMC article. Review.
There is increasing evidence regarding the prevalence of genetic cardiomyopathies, for which arrhythmias may be the first presentation. ...Sudden death can occur early in the course of these genetic cardiomyopathies, for which risk is not adequately tracked by left …
There is increasing evidence regarding the prevalence of genetic cardiomyopathies, for which arrhythmias may be the first presentatio …
Recent Findings Related to Cardiomyopathy and Genetics.
Yamada T, Nomura S. Yamada T, et al. Int J Mol Sci. 2021 Nov 20;22(22):12522. doi: 10.3390/ijms222212522. Int J Mol Sci. 2021. PMID: 34830403 Free PMC article. Review.
Rare variants have been shown to play major roles in the pathogenesis of cardiomyopathy, which was empirically recognized as a monogenic disease, and it has been elucidated that the clinical course of cardiomyopathy varies depending on the causative genes. These findings were not …
Rare variants have been shown to play major roles in the pathogenesis of cardiomyopathy, which was empirically recognized as a monogenic dis …
Classification, Epidemiology, and Global Burden of Cardiomyopathies.
McKenna WJ, Maron BJ, Thiene G. McKenna WJ, et al. Circ Res. 2017 Sep 15;121(7):722-730. doi: 10.1161/CIRCRESAHA.117.309711. Circ Res. 2017. PMID: 28912179 Review.
Nearly, 50% of patients dying suddenly in childhood or adolescence or undergoing cardiac transplantation are affected by cardiomyopathies. Novel cardiomyopathies have been discovered (arrhythmogenic, restrictive, and noncompacted) and added to update the World Healt …
Nearly, 50% of patients dying suddenly in childhood or adolescence or undergoing cardiac transplantation are affected by cardiomyopathies …
[Dilated myocardiopathy].
García Morán JI. García Morán JI. Med Clin (Barc). 1994 Nov 12;103(16):638. Med Clin (Barc). 1994. PMID: 7996925 Spanish. No abstract available.
22,657 results
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