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2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM 3rd, Hua W, Indik JH, Ingles J, James CA, John RM, Judge DP, Keegan R, Krahn AD, Link MS, Marcus FI, McLeod CJ, Mestroni L, Priori SG, Saffitz JE, Sanatani S, Shimizu W, van Tintelen JP, Wilde AAM, Zareba W. Towbin JA, et al. Heart Rhythm. 2019 Nov;16(11):e301-e372. doi: 10.1016/j.hrthm.2019.05.007. Epub 2019 May 9. Heart Rhythm. 2019. PMID: 31078652
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloidosis, sarcoidosis, Chagas disease, and left ventricular noncompaction. The ACM phenotype overlaps with other cardiomyopathi …
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloid …
Genetic profile and genotype-phenotype correlations in childhood cardiomyopathy.
Wanert C, El Louali F, Al Dybiat S, Nguyen K, Zaffran S, Ovaert C. Wanert C, et al. Arch Cardiovasc Dis. 2023 Jun-Jul;116(6-7):309-315. doi: 10.1016/j.acvd.2023.04.008. Epub 2023 May 16. Arch Cardiovasc Dis. 2023. PMID: 37246080 Free article.
METHODS: We performed a retrospective study of all patients with idiopathic cardiomyopathy aged<18years in Southeast France. Secondary causes of cardiomyopathy were excluded. All data (clinical, echocardiography, genetic testing) were collected retrospectively. P …
METHODS: We performed a retrospective study of all patients with idiopathic cardiomyopathy aged<18years in Southeast France. Secon …
Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.
Beckmann BM, Pfeufer A, Kääb S. Beckmann BM, et al. Dtsch Arztebl Int. 2011 Sep;108(37):623-33; quiz 634. doi: 10.3238/arztebl.2011.0623. Epub 2011 Sep 16. Dtsch Arztebl Int. 2011. PMID: 21977220 Free PMC article. Review.
BACKGROUND: The incidence of sudden cardiac death in persons under age 40 is roughly 3 per 100 000 persons per year in Germany and North America. Many of these deaths are found to be due to hereditary heart diseases, often a primary structural heart disease associat …
BACKGROUND: The incidence of sudden cardiac death in persons under age 40 is roughly 3 per 100 000 persons per year in Germany and North Ame …
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
Teekakirikul P, Kelly MA, Rehm HL, Lakdawala NK, Funke BH. Teekakirikul P, et al. J Mol Diagn. 2013 Mar;15(2):158-70. doi: 10.1016/j.jmoldx.2012.09.002. Epub 2012 Dec 27. J Mol Diagn. 2013. PMID: 23274168 Free article. Review.
Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, left ventricular noncompaction, and restrictive cardiomyopathy. ...Remaining cha …
Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic right …
Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies.
Nguyen Q, Lim KRQ, Yokota T. Nguyen Q, et al. Int J Mol Sci. 2020 Jan 22;21(3):733. doi: 10.3390/ijms21030733. Int J Mol Sci. 2020. PMID: 31979133 Free PMC article. Review.
Cardiomyopathies are diseases of heart muscle, a significant percentage of which are genetic in origin. Cardiomyopathies can be classified as dilated, hypertrophic, restrictive, arrhythmogenic right ventricular or left ventricular non-com …
Cardiomyopathies are diseases of heart muscle, a significant percentage of which are genetic in origin. Cardiomyopathies …
Presentation, diagnosis, and medical management of heart failure in children: Canadian Cardiovascular Society guidelines.
Kantor PF, Lougheed J, Dancea A, McGillion M, Barbosa N, Chan C, Dillenburg R, Atallah J, Buchholz H, Chant-Gambacort C, Conway J, Gardin L, George K, Greenway S, Human DG, Jeewa A, Price JF, Ross RD, Roche SL, Ryerson L, Soni R, Wilson J, Wong K; Children's Heart Failure Study Group. Kantor PF, et al. Can J Cardiol. 2013 Dec;29(12):1535-52. doi: 10.1016/j.cjca.2013.08.008. Can J Cardiol. 2013. PMID: 24267800
Pediatric heart failure (HF) is an important cause of morbidity and mortality in childhood. ...This work does not include Recommendations for advanced management involving ventricular assist devices, or other device therapies....
Pediatric heart failure (HF) is an important cause of morbidity and mortality in childhood. ...This work does not include Recommendat …
Ventricular non-compaction cardiomyopathy: prenatal diagnosis and pathology.
Tian L, Zhou Q, Zhou J, Zeng S, Cao D, Zhang M. Tian L, et al. Prenat Diagn. 2015 Mar;35(3):221-7. doi: 10.1002/pd.4523. Epub 2014 Dec 12. Prenat Diagn. 2015. PMID: 25346355
Among the nine fetuses with a prenatal diagnosis of NCCM, six were diagnosed with left ventricular non-compaction (LVNC), two with non-compaction of both ventricles (biventricular NCCM), and one with right ventricular non-compaction. ...Fetal non-compa …
Among the nine fetuses with a prenatal diagnosis of NCCM, six were diagnosed with left ventricular non-compaction (LVNC), two with no …
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary.
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM 3rd, Hua W, Indik JH, Ingles J, James CA, John RM, Judge DP, Keegan R, Krahn AD, Link MS, Marcus FI, McLeod CJ, Mestroni L, Priori SG, Saffitz JE, Sanatani S, Shimizu W, van Tintelen JP, Wilde AAM, Zareba W. Towbin JA, et al. Heart Rhythm. 2019 Nov;16(11):e373-e407. doi: 10.1016/j.hrthm.2019.09.019. Heart Rhythm. 2019. PMID: 31676023
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloidosis, sarcoidosis, Chagas disease, and left ventricular noncompaction. The ACM phenotype overlaps with other cardiomyopathi …
This designation includes, but is not limited to, arrhythmogenic right/left ventricular cardiomyopathy, cardiac amyloid …
Role of Imaging in the Evaluation of Patients at Risk for Sudden Cardiac Death: Genotype-Phenotype Intersection.
Nagueh SF, Zoghbi WA. Nagueh SF, et al. JACC Cardiovasc Imaging. 2015 Jul;8(7):828-45. doi: 10.1016/j.jcmg.2015.04.006. JACC Cardiovasc Imaging. 2015. PMID: 26183555 Free article. Review.
These include primary electrophysiological disorders (long QT, short QT, Brugada, and catecholaminergic ventricular tachycardia syndromes) and cardiomyopathies, including hypertrophic and dilated cardiomyopathy and arrhythmogenic right ventricular …
These include primary electrophysiological disorders (long QT, short QT, Brugada, and catecholaminergic ventricular tachycardia syndr …
Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.
Hershberger RE, Lindenfeld J, Mestroni L, Seidman CE, Taylor MR, Towbin JA; Heart Failure Society of America. Hershberger RE, et al. J Card Fail. 2009 Mar;15(2):83-97. doi: 10.1016/j.cardfail.2009.01.006. J Card Fail. 2009. PMID: 19254666
Substantial progress has been made recently in understanding the genetic basis of cardiomyopathy. Cardiomyopathies with known genetic cause include hypertrophic (HCM), dilated (DCM), restrictive (RCM), arrhythmogenic right ventricular dysplasia/card …
Substantial progress has been made recently in understanding the genetic basis of cardiomyopathy. Cardiomyopathies with known …
14 results