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

Year Number of Results
1980 1
1982 2
1983 4
1984 14
1985 18
1986 20
1987 19
1988 50
1989 56
1990 70
1991 65
1992 59
1993 77
1994 77
1995 79
1996 83
1997 68
1998 69
1999 75
2000 129
2001 99
2002 122
2003 96
2004 118
2005 125
2006 117
2007 91
2008 116
2009 89
2010 113
2011 97
2012 95
2013 107
2014 100
2015 119
2016 93
2017 106
2018 98
2019 110
2020 112
2021 106
2022 98
2023 100
2024 28

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3,260 results

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Page 1
Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches.
Heymans S, Lakdawala NK, Tschöpe C, Klingel K. Heymans S, et al. Lancet. 2023 Sep 16;402(10406):998-1011. doi: 10.1016/S0140-6736(23)01241-2. Lancet. 2023. PMID: 37716772 Review.
Dilated cardiomyopathy is conventionally defined as the presence of left ventricular or biventricular dilatation or systolic dysfunction in the absence of abnormal loading conditions (eg, primary valve disease) or significant coronary artery disease sufficient to ca …
Dilated cardiomyopathy is conventionally defined as the presence of left ventricular or biventricular dilatation or systolic d …
The Diagnosis and Evaluation of Dilated Cardiomyopathy.
Japp AG, Gulati A, Cook SA, Cowie MR, Prasad SK. Japp AG, et al. J Am Coll Cardiol. 2016 Jun 28;67(25):2996-3010. doi: 10.1016/j.jacc.2016.03.590. J Am Coll Cardiol. 2016. PMID: 27339497 Free article. Review.
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insults. ...
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmenta …
Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments.
Orphanou N, Papatheodorou E, Anastasakis A. Orphanou N, et al. Heart Fail Rev. 2022 Jul;27(4):1173-1191. doi: 10.1007/s10741-021-10139-0. Epub 2021 Jul 14. Heart Fail Rev. 2022. PMID: 34263412 Free PMC article. Review.
Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and non-genetic etiologies, leading to left ventricular systolic dysfunction and dilatation, not explained by abnormal loading conditions or coronary artery disease. ...
Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and non-genetic etiologies, leading to le …
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.
McNally EM, Mestroni L. McNally EM, et al. Circ Res. 2017 Sep 15;121(7):731-748. doi: 10.1161/CIRCRESAHA.116.309396. Circ Res. 2017. PMID: 28912180 Free PMC article. Review.
Nonischemic dilated cardiomyopathy (DCM) often has a genetic pathogenesis. Because of the large number of genes and alleles attributed to DCM, comprehensive genetic testing encompasses ever-increasing gene panels. ...Historically, cardiac morphology has been used to …
Nonischemic dilated cardiomyopathy (DCM) often has a genetic pathogenesis. Because of the large number of genes and alleles at …
Evolving concepts in dilated cardiomyopathy.
Merlo M, Cannatà A, Gobbo M, Stolfo D, Elliott PM, Sinagra G. Merlo M, et al. Eur J Heart Fail. 2018 Feb;20(2):228-239. doi: 10.1002/ejhf.1103. Epub 2017 Dec 22. Eur J Heart Fail. 2018. PMID: 29271570 Free article. Review.
Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic background and usually affects young patients with few co-morbidities. ...
Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic backgro …
Dilated cardiomyopathy.
Weintraub RG, Semsarian C, Macdonald P. Weintraub RG, et al. Lancet. 2017 Jul 22;390(10092):400-414. doi: 10.1016/S0140-6736(16)31713-5. Epub 2017 Feb 10. Lancet. 2017. PMID: 28190577 Review.
Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction. ...
Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction. ...
Dilated cardiomyopathy and chronic cardiac inflammation: Pathogenesis, diagnosis and therapy.
Harding D, Chong MHA, Lahoti N, Bigogno CM, Prema R, Mohiddin SA, Marelli-Berg F. Harding D, et al. J Intern Med. 2023 Jan;293(1):23-47. doi: 10.1111/joim.13556. Epub 2022 Aug 27. J Intern Med. 2023. PMID: 36030368 Review.
Dilated cardiomyopathy (DCM) is typically defined by left ventricular dilation and systolic dysfunction in the absence of a clear precipitant. ...
Dilated cardiomyopathy (DCM) is typically defined by left ventricular dilation and systolic dysfunction in the absence of a cl …
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.
While ventricular arrhythmias are well-recognized as presentation for arrhythmogenic cardiomyopathy in the right ventricle, the scope of arrhythmogenic cardiomyopathy has broadened to include those with dominant left ventricular involvement, usually with a phenotype …
While ventricular arrhythmias are well-recognized as presentation for arrhythmogenic cardiomyopathy in the right ventricle, the scope …
Dilated cardiomyopathy: from epidemiologic to genetic phenotypes: A translational review of current literature.
Reichart D, Magnussen C, Zeller T, Blankenberg S. Reichart D, et al. J Intern Med. 2019 Oct;286(4):362-372. doi: 10.1111/joim.12944. Epub 2019 Jul 29. J Intern Med. 2019. PMID: 31132311 Free article. Review.
Dilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and, consecutively, contractile dysfunction. ...
Dilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and, consecutively, contractile dysfunction. ...
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.
Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction. ...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondar …
3,260 results