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

Year Number of Results
1995 1
1996 1
1998 1
2000 1
2003 1
2008 2
2012 1
2016 1
2017 1
2018 1
2020 1
2023 0

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11 results

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Page 1
Arrhythmogenic right ventricular dysplasia.
Fontaine G. Fontaine G. Curr Opin Cardiol. 1995 Jan;10(1):16-20. doi: 10.1097/00001573-199501000-00004. Curr Opin Cardiol. 1995. PMID: 7787258 Review.
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more frequently recognized. ...In some patients, a superimposed inflammatory process mixed with the pattern of arrhythmogenic right …
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more …
The role of genetics in cardiovascular disease: arrhythmogenic cardiomyopathy.
James CA, Syrris P, van Tintelen JP, Calkins H. James CA, et al. Eur Heart J. 2020 Apr 7;41(14):1393-1400. doi: 10.1093/eurheartj/ehaa141. Eur Heart J. 2020. PMID: 32191298 Review.
Arrhythmogenic cardiomyopathy (ACM) is a heritable cardiomyopathy characterized by frequent ventricular arrhythmias and progressive ventricular dysfunction. ...We also review best practices for integrating genetics-including recent discoveries-in caring for A …
Arrhythmogenic cardiomyopathy (ACM) is a heritable cardiomyopathy characterized by frequent ventricular arrhythmias and progre …
Pathology and pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
Thiene G, Basso C, Calabrese F, Angelini A, Valente M. Thiene G, et al. Herz. 2000 May;25(3):210-5. doi: 10.1007/s000590050008. Herz. 2000. PMID: 10904840 Review.
Arrhythmogenic right ventricular cardiomyopathy is a primary heart muscle disease characterized by progressive myocardial atrophy of the right ventricle, with transmural fatty or fibrofatty replacement, either segmental or diffuse, accounting for elect …
Arrhythmogenic right ventricular cardiomyopathy is a primary heart muscle disease characterized by progressive myocardi …
Diagnostic Criteria, Genetics, and Molecular Basis of Arrhythmogenic Cardiomyopathy.
Basso C, Pilichou K, Bauce B, Corrado D, Thiene G. Basso C, et al. Heart Fail Clin. 2018 Apr;14(2):201-213. doi: 10.1016/j.hfc.2018.01.002. Heart Fail Clin. 2018. PMID: 29525648 Review.
Arrhythmogenic cardiomyopathy (AC) is an inherited heart muscle disease characterized by myocardial atrophy and fibrofatty replacement of the ventricular myocardium, at risk of sudden cardiac death, particularly in the young and athletes. Because there is no "gold s …
Arrhythmogenic cardiomyopathy (AC) is an inherited heart muscle disease characterized by myocardial atrophy and fibrofatty replacemen …
Grey zones in cardiomyopathies: defining boundaries between genetic and iatrogenic disease.
Quarta G, Papadakis M, Donna PD, Maurizi N, Iacovoni A, Gavazzi A, Senni M, Olivotto I. Quarta G, et al. Nat Rev Cardiol. 2017 Feb;14(2):102-112. doi: 10.1038/nrcardio.2016.175. Epub 2016 Nov 10. Nat Rev Cardiol. 2017. PMID: 27830773 Review.
In this Review, three of the most common and controversial areas are discussed, including left ventricular hypertrophy; left ventricular dilatation, noncompaction, and fibrosis; and arrhythmias originating from the right ventricle. ...
In this Review, three of the most common and controversial areas are discussed, including left ventricular hypertrophy; left ventr …
Overview of inherited metabolic disorders causing cardiovascular disease.
Wilcken DE. Wilcken DE. J Inherit Metab Dis. 2003;26(2-3):245-57. doi: 10.1023/a:1024445402983. J Inherit Metab Dis. 2003. PMID: 12889664 Review.
An important recently established cause of cardiomyopathy is carnitine transporter defect; it is treated effectively with oral carnitine. The autosomal dominant arrhythmogenic right ventricular dysplasia occurs with a prevalence of about 1 in 15,000 an …
An important recently established cause of cardiomyopathy is carnitine transporter defect; it is treated effectively with oral carnitine. Th …
Family history: an essential tool for cardiovascular genetic medicine.
Morales A, Cowan J, Dagua J, Hershberger RE. Morales A, et al. Congest Heart Fail. 2008 Jan-Feb;14(1):37-45. doi: 10.1111/j.1751-7133.2008.08201.x. Congest Heart Fail. 2008. PMID: 18256568 Free article. Review.
We will first focus on the most tractable diagnoses to apply the principles of cardiovascular genetic medicine: the cardiomyopathies such as dilated, hypertrophic, arrhythmogenic right ventricular dysplasia/cardiomyopathy and the channelopathies such a …
We will first focus on the most tractable diagnoses to apply the principles of cardiovascular genetic medicine: the cardiomyopathies such as …
Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations.
Cowan J, Morales A, Dagua J, Hershberger RE. Cowan J, et al. Congest Heart Fail. 2008 Mar-Apr;14(2):97-105. doi: 10.1111/j.1751-7133.2008.08217.x. Congest Heart Fail. 2008. PMID: 18401220 Free article. Review.
A previous article in the Cardiovascular Genetic Medicine: Clinical Perspectives and Future Applications series(1) highlighted an increasing recognition of the cardiomyopathies (hypertrophic [HCM], dilated [DCM], arrhythmogenic right ventricular dysplasia …
A previous article in the Cardiovascular Genetic Medicine: Clinical Perspectives and Future Applications series(1) highlighted an increasing …
The genetics of cardiac disease associated with sudden cardiac death: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology.
Perrin MJ, Gollob MH. Perrin MJ, et al. J Mol Diagn. 2012 Sep;14(5):424-36. doi: 10.1016/j.jmoldx.2012.04.002. Epub 2012 Jun 27. J Mol Diagn. 2012. PMID: 22749884 Free article. Review.
Sudden cardiac death due to ventricular arrhythmia most commonly occurs in the setting of coronary artery disease. ...Arrhythmia in such conditions may result from genetically mediated structural heart disease (eg, hypertrophic cardiomyopathy and arrhythmogenic r …
Sudden cardiac death due to ventricular arrhythmia most commonly occurs in the setting of coronary artery disease. ...Arrhythmia in s …
Genetic factors in dilated cardiomyopathy.
Mestroni L, Milasin J, Vatta M, Pinamonti B, Sinagra G, Rocco C, Matulic M, Falaschi A, Giacca M, Camerini F. Mestroni L, et al. Arch Mal Coeur Vaiss. 1996 Jul;89 Spec No 2:15-20. Arch Mal Coeur Vaiss. 1996. PMID: 8881501 Review.
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathogenesis of idiopathic dilated cardiomyopathy (IDC). In clinical surveys, a familial trait has been demonstrated in 20 to 30% of idiopathic dilated cardiomyopathy patients ( …
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathogenesis of idiopathic dilated cardiomyopat …
11 results