566 related articles for article (PubMed ID: 19254666)
1. Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.
Hershberger RE; Lindenfeld J; Mestroni L; Seidman CE; Taylor MR; Towbin JA;
J Card Fail; 2009 Mar; 15(2):83-97. PubMed ID: 19254666
[TBL] [Abstract][Full Text] [Related]
2. Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies.
Teo LY; Moran RT; Tang WH
Curr Heart Fail Rep; 2015 Dec; 12(6):339-49. PubMed ID: 26472190
[TBL] [Abstract][Full Text] [Related]
3. Inflammatory dilated cardiomyopathy (DCMI).
Maisch B; Richter A; Sandmöller A; Portig I; Pankuweit S;
Herz; 2005 Sep; 30(6):535-44. PubMed ID: 16170686
[TBL] [Abstract][Full Text] [Related]
4. The Feline Cardiomyopathies: 3. Cardiomyopathies other than HCM.
Kittleson MD; Côté E
J Feline Med Surg; 2021 Nov; 23(11):1053-1067. PubMed ID: 34693805
[TBL] [Abstract][Full Text] [Related]
5. [MR imaging in cardiomyopathies].
Miller S; Riessen R
Rofo; 2005 Nov; 177(11):1497-505. PubMed ID: 16302130
[TBL] [Abstract][Full Text] [Related]
6. Molecular mechanisms of inherited cardiomyopathies.
Fatkin D; Graham RM
Physiol Rev; 2002 Oct; 82(4):945-80. PubMed ID: 12270949
[TBL] [Abstract][Full Text] [Related]
7. Arrhythmogenic right ventricular dysplasia/cardiomyopathy.
El Masry HZ; Yadav AV
Expert Rev Cardiovasc Ther; 2008 Feb; 6(2):249-60. PubMed ID: 18248278
[TBL] [Abstract][Full Text] [Related]
8. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.
Monserrat L; Hermida-Prieto M; Fernandez X; Rodríguez I; Dumont C; Cazón L; Cuesta MG; Gonzalez-Juanatey C; Peteiro J; Alvarez N; Penas-Lado M; Castro-Beiras A
Eur Heart J; 2007 Aug; 28(16):1953-61. PubMed ID: 17611253
[TBL] [Abstract][Full Text] [Related]
9. [Genetics of inherited cardiomyopathies].
Richard P; Fressart V; Charron P; Hainque B
Pathol Biol (Paris); 2010 Oct; 58(5):343-52. PubMed ID: 19942368
[TBL] [Abstract][Full Text] [Related]
10. Molecular and cellular aspects of troponin cardiomyopathies.
Gomes AV; Potter JD
Ann N Y Acad Sci; 2004 May; 1015():214-24. PubMed ID: 15201162
[TBL] [Abstract][Full Text] [Related]
11. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.
Hoedemaekers YM; Caliskan K; Michels M; Frohn-Mulder I; van der Smagt JJ; Phefferkorn JE; Wessels MW; ten Cate FJ; Sijbrands EJ; Dooijes D; Majoor-Krakauer DF
Circ Cardiovasc Genet; 2010 Jun; 3(3):232-9. PubMed ID: 20530761
[TBL] [Abstract][Full Text] [Related]
12. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
Teekakirikul P; Kelly MA; Rehm HL; Lakdawala NK; Funke BH
J Mol Diagn; 2013 Mar; 15(2):158-70. PubMed ID: 23274168
[TBL] [Abstract][Full Text] [Related]
13. Molecular mechanisms in cardiomyopathy.
Dadson K; Hauck L; Billia F
Clin Sci (Lond); 2017 Jul; 131(13):1375-1392. PubMed ID: 28645928
[TBL] [Abstract][Full Text] [Related]
14. Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype.
Ashrafian H; Watkins H
J Am Coll Cardiol; 2007 Mar; 49(12):1251-64. PubMed ID: 17394955
[TBL] [Abstract][Full Text] [Related]
15. Cardiomyopathy Phenotypes and Outcomes for Children With Left Ventricular Myocardial Noncompaction: Results From the Pediatric Cardiomyopathy Registry.
Jefferies JL; Wilkinson JD; Sleeper LA; Colan SD; Lu M; Pahl E; Kantor PF; Everitt MD; Webber SA; Kaufman BD; Lamour JM; Canter CE; Hsu DT; Addonizio LJ; Lipshultz SE; Towbin JA;
J Card Fail; 2015 Nov; 21(11):877-84. PubMed ID: 26164213
[TBL] [Abstract][Full Text] [Related]
16. Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies.
Mazzarotto F; Hawley MH; Beltrami M; Beekman L; de Marvao A; McGurk KA; Statton B; Boschi B; Girolami F; Roberts AM; Lodder EM; Allouba M; Romeih S; Aguib Y; Baksi AJ; Pantazis A; Prasad SK; Cerbai E; Yacoub MH; O'Regan DP; Cook SA; Ware JS; Funke B; Olivotto I; Bezzina CR; Barton PJR; Walsh R
Genet Med; 2021 May; 23(5):856-864. PubMed ID: 33500567
[TBL] [Abstract][Full Text] [Related]
17. ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients.
Heliö T; Elliott P; Koskenvuo JW; Gimeno JR; Tavazzi L; Tendera M; Kaski JP; Mansencal N; Bilińska Z; Carr-White G; Damy T; Frustaci A; Kindermann I; Ripoll-Vera T; Čelutkienė J; Axelsson A; Lorenzini M; Saad A; Maggioni AP; Laroche C; Caforio ALP; Charron P;
ESC Heart Fail; 2020 Oct; 7(5):3013-3021. PubMed ID: 32767651
[TBL] [Abstract][Full Text] [Related]
18. Review: Metabolic cardiomyopathy and conduction system defects in children.
Gilbert-Barness E
Ann Clin Lab Sci; 2004; 34(1):15-34. PubMed ID: 15038665
[TBL] [Abstract][Full Text] [Related]
19. The clinical profile, genetic basis and survival of childhood cardiomyopathy: a single-center retrospective study.
Yuan W; Jia Z; Li J; Liu L; Tian J; Huang X; Quan J
Eur J Pediatr; 2024 Mar; 183(3):1389-1401. PubMed ID: 38165464
[TBL] [Abstract][Full Text] [Related]
20. Arrhythmogenic right ventricular dysplasia/cardiomyopathy-three decades of progress.
Calkins H
Circ J; 2015; 79(5):901-13. PubMed ID: 25877738
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]