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Page 1
Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management.
Peters S, Kumar S, Elliott P, Kalman JM, Fatkin D. Peters S, et al. Heart Lung Circ. 2019 Jan;28(1):31-38. doi: 10.1016/j.hlc.2018.09.010. Epub 2018 Oct 11. Heart Lung Circ. 2019. PMID: 30482687 Review.
Cardiac arrhythmias are frequently seen in patients with dilated cardiomyopathy (DCM) and can precipitate heart failure and death. In patients with non-ischaemic DCM, evidence for the benefit of an implantable cardioverter-defibrillator (ICD) for primary prev …
Cardiac arrhythmias are frequently seen in patients with dilated cardiomyopathy (DCM) and can precipitate heart failure and de …
[Familial dilated cardiomyopathy].
Osterziel KJ, Hassfeld S, Geier C, Perrot A. Osterziel KJ, et al. Herz. 2005 Sep;30(6):529-34. doi: 10.1007/s00059-005-2732-3. Herz. 2005. PMID: 16170685 Review. German.
Dilated cardiomyopathy (DCM) is the most frequent form of primary myocardial diseases and the third most common cause of heart failure. ...Until then, clinical examination of family members and, in case of familial DCM, genetic counseling are recommend …
Dilated cardiomyopathy (DCM) is the most frequent form of primary myocardial diseases and the third most common cause o …
Genetic Testing as a Guide for Treatment in Dilated Cardiomyopathies.
García-Hernandez S, Iglesias LM. García-Hernandez S, et al. Curr Cardiol Rep. 2022 Nov;24(11):1537-1546. doi: 10.1007/s11886-022-01772-8. Epub 2022 Aug 22. Curr Cardiol Rep. 2022. PMID: 35994197 Review.
PURPOSE OF REVIEW: Dilated cardiomyopathy (DCM) is one of the most prevalent primary cardiomyopathies and may be caused by genetic and non-genetic etiologies. ...The identification of the genetic substrate underlying dilated cardiomyopathy makes …
PURPOSE OF REVIEW: Dilated cardiomyopathy (DCM) is one of the most prevalent primary cardiomyopathies and may be caused …
Atrial fibrillation in patients with inherited cardiomyopathies.
Yeung C, Enriquez A, Suarez-Fuster L, Baranchuk A. Yeung C, et al. Europace. 2019 Jan 1;21(1):22-32. doi: 10.1093/europace/euy064. Europace. 2019. PMID: 29684120 Review.
Atrial fibrillation (AF) often complicates the course of inherited cardiomyopathies and, in some cases, may be the presenting feature. Each inherited cardiomyopathy has its own peculiar pathogenetic characteristics that can contribute to the development and maintenance of …
Atrial fibrillation (AF) often complicates the course of inherited cardiomyopathies and, in some cases, may be the presenting feature. Each …
Heart failure: advanced development in genetics and epigenetics.
Yang J, Xu WW, Hu SJ. Yang J, et al. Biomed Res Int. 2015;2015:352734. doi: 10.1155/2015/352734. Epub 2015 Apr 9. Biomed Res Int. 2015. PMID: 25949994 Free PMC article. Review.
Genetic mutations associated with familial dilated cardiomyopathy, hypertrophic cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy can contribute to the various pathologies of HF. ...This review gives an overview of genetic muta …
Genetic mutations associated with familial dilated cardiomyopathy, hypertrophic cardiomyopathy, and arrhythmogen …
Molecular and clinical aspects of inherited cardiomyopathies.
Durand JB, Abchee AB, Roberts R. Durand JB, et al. Ann Med. 1995 Jun;27(3):311-7. doi: 10.3109/07853899509002583. Ann Med. 1995. PMID: 7546620 Review.
Hypertrophic cardiomyopathy (HCM) is phenotypically and genotypically a heterogeneous disease. ...Familial dilated cardiomyopathy is thought to account for approximately 20% of the so-called cases of idiopathic DCM....
Hypertrophic cardiomyopathy (HCM) is phenotypically and genotypically a heterogeneous disease. ...Familial dilated c …
How do mutations in contractile proteins cause the primary familial cardiomyopathies?
Marston SB. Marston SB. J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266-2. Epub 2011 Mar 22. J Cardiovasc Transl Res. 2011. PMID: 21424860 Review.
In this article, the available evidence about the functional effects of the contractile protein mutations that cause hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) is assessed. The molecular mechanism of the contractile apparatus of cardia …
In this article, the available evidence about the functional effects of the contractile protein mutations that cause hypertrophic cardiom …
[Cardiomyopathies. I: classification of cardiomyopathies--dilated cardiomyopathy].
Schultheiss HP, Noutsias M, Kühl U, Lassner D, Gross U, Poller W, Pauschinger M. Schultheiss HP, et al. Internist (Berl). 2005 Nov;46(11):1245-56; quiz 1257. doi: 10.1007/s00108-005-1483-9. Internist (Berl). 2005. PMID: 16228156 Review. German.
Several gene mutations have been identified in genetic/familial dilated cardiomyopathy. First-degree relatives should be screened for early stages. Primary prevention of sudden cardiac death shows increasing superiority of the implantable defibrillator …
Several gene mutations have been identified in genetic/familial dilated cardiomyopathy. First-degree relatives should b …
A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.
Hertz CL, Ferrero-Miliani L, Frank-Hansen R, Morling N, Bundgaard H. Hertz CL, et al. Europace. 2015 Mar;17(3):350-7. doi: 10.1093/europace/euu210. Epub 2014 Oct 26. Europace. 2015. PMID: 25345827 Review.
In the case of SCD, the optimal establishment of the cause of death and management of the family call for standardized post-mortem procedures, genetic screening, and family screening. Studies of genetic testing in patients with primary arrhythmia disorders or cardiomyopath …
In the case of SCD, the optimal establishment of the cause of death and management of the family call for standardized post-mortem procedure …