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

Year Number of Results
1966 1
1967 2
1968 2
1970 5
1971 3
1972 3
1973 6
1974 1
1975 15
1976 8
1977 5
1978 7
1979 7
1980 3
1981 4
1982 6
1983 7
1984 18
1985 13
1986 10
1987 14
1988 16
1989 17
1990 21
1991 13
1992 15
1993 25
1994 18
1995 25
1996 22
1997 25
1998 25
1999 27
2000 26
2001 23
2002 20
2003 19
2004 32
2005 33
2006 36
2007 31
2008 65
2009 80
2010 65
2011 67
2012 93
2013 87
2014 65
2015 81
2016 65
2017 83
2018 79
2019 73
2020 87
2021 61
2022 32
2023 21
2024 15

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1,538 results

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Quoted phrase not found in phrase index: "Abnormal myocardium morphology"
Page 1
Arrhythmogenic right ventricular cardiomyopathy in dogs.
Cunningham SM, Dos Santos L. Cunningham SM, et al. J Vet Cardiol. 2022 Apr;40:156-169. doi: 10.1016/j.jvc.2021.07.001. Epub 2021 Jul 23. J Vet Cardiol. 2022. PMID: 34503916
A common entity in Boxers and the related English bulldog, the disease is characterized by fatty or fibrofatty replacement of the myocardium, ventricular arrhythmias, and the potential for syncope or sudden death. ...This article will review the pathophysiology, clinical d …
A common entity in Boxers and the related English bulldog, the disease is characterized by fatty or fibrofatty replacement of the myocard …
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. It is characterized by a 2-layer myocardium with an enlarged trabecular layer and a thinner compacted layer. The prevalence has been incr …
Left ventricular hypertrabeculation (LVHT) is a phenotype with multiple etiologies and variable clinical presentation and significance. It i …
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 can result from coronary artery abnormalities, tachyarrhythmias, exposure to infection or toxins, or secondary to other underlying disorders. ...This compendium summarizes current knowledge of the genetic and molecular origins, clinical course …
Pediatric cardiomyopathies can result from coronary artery abnormalities, tachyarrhythmias, exposure to infection or toxins, or secon …
Cirrhotic cardiomyopathy.
Ruiz-del-Árbol L, Serradilla R. Ruiz-del-Árbol L, et al. World J Gastroenterol. 2015 Nov 7;21(41):11502-21. doi: 10.3748/wjg.v21.i41.11502. World J Gastroenterol. 2015. PMID: 26556983 Free PMC article. Review.
During the course of cirrhosis, there is a progressive deterioration of cardiac function manifested by the disappearance of the hyperdynamic circulation due to a failure in heart function with decreased cardiac output. ...Other findings of this specific cardiomyopathy incl …
During the course of cirrhosis, there is a progressive deterioration of cardiac function manifested by the disappearance of the hyper …
Ebstein Anomaly in the Adult Patient.
Fuchs MM, Connolly HM. Fuchs MM, et al. Cardiol Clin. 2020 Aug;38(3):353-363. doi: 10.1016/j.ccl.2020.04.004. Epub 2020 Jun 6. Cardiol Clin. 2020. PMID: 32622490 Review.
Ebstein anomaly is a congenital malformation involving primarily the tricuspid valve, with failure of delamination from the underlying myocardium and right ventricular myopathy. Echocardiography is diagnostic in most patients and demonstrates apical displacement of …
Ebstein anomaly is a congenital malformation involving primarily the tricuspid valve, with failure of delamination from the underlyin …
Mitochondrial dynamics in diabetic cardiomyopathy.
Galloway CA, Yoon Y. Galloway CA, et al. Antioxid Redox Signal. 2015 Jun 10;22(17):1545-62. doi: 10.1089/ars.2015.6293. Epub 2015 Apr 13. Antioxid Redox Signal. 2015. PMID: 25738230 Free PMC article. Review.
Dysregulation of Ca(2+) handling, metabolic changes, and oxidative stress are observed in DCM, abnormalities reflected in alterations in mitochondrial energetics. Cardiac tissue from DCM patients also presents with altered mitochondrial morphology, suggesting a poss …
Dysregulation of Ca(2+) handling, metabolic changes, and oxidative stress are observed in DCM, abnormalities reflected in alterations …
An Overview of Diabetic Cardiomyopathy.
Quaiyoom A, Kumar R. Quaiyoom A, et al. Curr Diabetes Rev. 2024;20(5):e121023222139. doi: 10.2174/0115733998255538231001122639. Curr Diabetes Rev. 2024. PMID: 37842898 Review.
Diabetic cardiomyopathy (DCM) is a myocardial disorder that is characterised by structural and functional abnormalities of the heart muscle in the absence of hypertension, valvular heart disease, congenital heart defects, or coronary artery disease (CAD). ...A bioma …
Diabetic cardiomyopathy (DCM) is a myocardial disorder that is characterised by structural and functional abnormalities of the heart …
Cardiac imaging in Ebstein anomaly.
Qureshi MY, O'Leary PW, Connolly HM. Qureshi MY, et al. Trends Cardiovasc Med. 2018 Aug;28(6):403-409. doi: 10.1016/j.tcm.2018.01.002. Epub 2018 Jan 12. Trends Cardiovasc Med. 2018. PMID: 29409687 Review.
Ebstein anomaly is a congenital disorder of right ventricular myocardial development, which affects the tricuspid valve in addition to the right ventricular myocardium. ...
Ebstein anomaly is a congenital disorder of right ventricular myocardial development, which affects the tricuspid valve in addition t …
Congenitally corrected transposition.
Wallis GA, Debich-Spicer D, Anderson RH. Wallis GA, et al. Orphanet J Rare Dis. 2011 May 14;6:22. doi: 10.1186/1750-1172-6-22. Orphanet J Rare Dis. 2011. PMID: 21569592 Free PMC article. Review.
Incidence has been reported to be around 1/33,000 live births, accounting for approximately 0.05% of congenital heart malformations. Associated malformations may include interventricular communications, obstructions of the outlet from the morphologically left ventricle, an …
Incidence has been reported to be around 1/33,000 live births, accounting for approximately 0.05% of congenital heart malformations. …
Repair for Congenital Mitral Valve Stenosis.
Delmo Walter EM, Hetzer R. Delmo Walter EM, et al. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2018 Mar;21:46-57. doi: 10.1053/j.pcsu.2017.11.008. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2018. PMID: 29425525 Review.
In 48 patients, CMS is involved in Shone's anomaly. The typical congenital MS (type I) was seen in 56 patients. Hypoplastic MV (type II, n = 15) was associated with severe left ventricular outflow tract abnormalities and hypoplastic left ventricular cavity and muscl …
In 48 patients, CMS is involved in Shone's anomaly. The typical congenital MS (type I) was seen in 56 patients. Hypoplastic MV (type …
1,538 results