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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.
In patients with non-ischaemic DCM, evidence for the benefit of an implantable cardioverter-defibrillator (ICD) for primary prevention of sudden cardiac death has recently been questioned. ...Malignant ventricular arrhythmias often occur as a nonspecific consequence of DCM …
In patients with non-ischaemic DCM, evidence for the benefit of an implantable cardioverter-defibrillator (ICD) for primary preventio …
[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. ...
Dilated cardiomyopathy (DCM) is the most frequent form of primary myocardial diseases and the third most common cause of heart failur …
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. ...
PURPOSE OF REVIEW: Dilated cardiomyopathy (DCM) is one of the most prevalent primary cardiomyopathies and may be caused by genetic an …
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 may occur as a consequence of disease-specific defects, non-specific cardiac chamber changes secondary to the primary illness, or a combination thereof. The presence of AF can denote a turning point in the progression of the disease, promoting clinical …
Atrial fibrillation may occur as a consequence of disease-specific defects, non-specific cardiac chamber changes secondary to the primary
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.
Heart failure (HF) is a complex pathophysiological syndrome that arises from a primary defect in the ability of the heart to take in and/or eject sufficient blood. Genetic mutations associated with familial dilated cardiomyopathy, hypertrophic cardiomy …
Heart failure (HF) is a complex pathophysiological syndrome that arises from a primary defect in the ability of the heart to take in …
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.
The molecular basis of the pathogenesis of the cardiac hypertrophy appears to be a compensatory response to the primary defect. In addition to providing a definitive presymptomatic diagnosis, studies correlating beta-MHC mutations with clinical prognosis suggest they have …
The molecular basis of the pathogenesis of the cardiac hypertrophy appears to be a compensatory response to the primary defect. In ad …
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 …
[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 studies have shown that specific immunomodulatory treatment options can halt the progressive course of the disease. Several gene mutations have been identified in genetic/familial dilated cardiomyopathy. First-degree relatives should be screened for e …
Several studies have shown that specific immunomodulatory treatment options can halt the progressive course of the disease. Several gene mut …