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

Year Number of Results
1971 2
1974 1
1975 1
1976 1
1980 4
1981 1
1984 2
1985 2
1986 2
1987 3
1988 8
1989 9
1990 17
1991 7
1992 16
1993 13
1994 12
1995 26
1996 17
1997 28
1998 22
1999 18
2000 46
2001 28
2002 33
2003 29
2004 37
2005 48
2006 47
2007 32
2008 39
2009 47
2010 47
2011 30
2012 53
2013 53
2014 57
2015 89
2016 68
2017 73
2018 63
2019 57
2020 70
2021 61
2022 64
2023 52
2024 12

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Search Results

1,320 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.
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 …
Anatomy, Function, and Dysfunction of the Right Ventricle: JACC State-of-the-Art Review.
Sanz J, Sánchez-Quintana D, Bossone E, Bogaard HJ, Naeije R. Sanz J, et al. J Am Coll Cardiol. 2019 Apr 2;73(12):1463-1482. doi: 10.1016/j.jacc.2018.12.076. J Am Coll Cardiol. 2019. PMID: 30922478 Free article. Review.
There is increasing recognition of the crucial role of the right ventricle (RV) in determining functional status and prognosis in multiple conditions. The normal RV is anatomically and functionally different from the left ventricle, which precludes direct extrapolation of …
There is increasing recognition of the crucial role of the right ventricle (RV) in determining functional status and prognosis in mul …
Arrhythmogenic Cardiomyopathy.
Corrado D, Basso C, Judge DP. Corrado D, et al. Circ Res. 2017 Sep 15;121(7):784-802. doi: 10.1161/CIRCRESAHA.117.309345. Circ Res. 2017. PMID: 28912183 Review.
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myoca …
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in you …
Septic Cardiomyopathy: From Pathophysiology to the Clinical Setting.
Carbone F, Liberale L, Preda A, Schindler TH, Montecucco F. Carbone F, et al. Cells. 2022 Sep 11;11(18):2833. doi: 10.3390/cells11182833. Cells. 2022. PMID: 36139408 Free PMC article. Review.
The onset of cardiomyopathy is a common feature in sepsis, with relevant effects on its pathophysiology and clinical care. Septic cardiomyopathy is characterized by reduced left ventricular (LV) contractility eventually associated with LV dilatation with or w …
The onset of cardiomyopathy is a common feature in sepsis, with relevant effects on its pathophysiology and clinical care. Septic …
Pacing-induced cardiomyopathy: A systematic review and meta-analysis of definition, prevalence, risk factors, and management.
Somma V, Ha FJ, Palmer S, Mohamed U, Agarwal S. Somma V, et al. Heart Rhythm. 2023 Feb;20(2):282-290. doi: 10.1016/j.hrthm.2022.09.019. Epub 2022 Nov 7. Heart Rhythm. 2023. PMID: 36356656 Review.
Pacing-induced cardiomyopathy is a potential complication of right ventricular pacing. ...In meta-analysis, risk factors included male sex, history of myocardial infarction, chronic kidney disease, atrial fibrillation, baseline left ventricular ejectio …
Pacing-induced cardiomyopathy is a potential complication of right ventricular pacing. ...In meta-analysis, risk factor …
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 …
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 cr …
The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/250) and arrhythmogenic …
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, usu …
While ventricular arrhythmias are well-recognized as presentation for arrhythmogenic cardiomyopathy in the right ventri …
Septic cardiomyopathy: A narrative review.
Lima MR, Silva D. Lima MR, et al. Rev Port Cardiol. 2023 May;42(5):471-481. doi: 10.1016/j.repc.2021.05.020. Epub 2023 Mar 7. Rev Port Cardiol. 2023. PMID: 36893835 Free article. Review. English, Portuguese.
Sepsis-induced myocardial dysfunction (SIMD), present in more than 50% of septic patients, is characterized by (i) left ventricular (LV) dilatation with normal or low filling pressure, (ii) right and/or LV (systolic and/or diastolic) dysfunction and (iii) reversibil …
Sepsis-induced myocardial dysfunction (SIMD), present in more than 50% of septic patients, is characterized by (i) left ventricular ( …
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy.
Corrado D, Zorzi A, Cipriani A, Bauce B, Bariani R, Beffagna G, De Lazzari M, Migliore F, Pilichou K, Rampazzo A, Rigato I, Rizzo S, Thiene G, Perazzolo Marra M, Basso C. Corrado D, et al. J Am Heart Assoc. 2021 Sep 21;10(18):e021987. doi: 10.1161/JAHA.121.021987. Epub 2021 Sep 17. J Am Heart Assoc. 2021. PMID: 34533054 Free PMC article. Review.
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (arrhythmogenic right ventricular cardiomyopathy), they lacked sensitivity for identification of the expanding phenotypic spe …
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (arrhy …
1,320 results