These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. [Advances in the molecular pathogenesis of hypertrophic cardiomyopathy]. Song YR; Liu Z; Gu SL; Qian LJ; Yan QF Yi Chuan; 2011 Jun; 33(6):549-57. PubMed ID: 21684859 [TBL] [Abstract][Full Text] [Related]
7. Phenotypic Spectrum of Subclinical Sarcomere-Related Hypertrophic Cardiomyopathy and Transition to Overt Disease. Topriceanu CC; Moon JC; Axelsson Raja A; Captur G; Ho CY Circ Genom Precis Med; 2024 Aug; 17(4):e004580. PubMed ID: 38910555 [TBL] [Abstract][Full Text] [Related]
8. Deficient cMyBP-C protein expression during cardiomyocyte differentiation underlies human hypertrophic cardiomyopathy cellular phenotypes in disease specific human ES cell derived cardiomyocytes. Monteiro da Rocha A; Guerrero-Serna G; Helms A; Luzod C; Mironov S; Russell M; Jalife J; Day SM; Smith GD; Herron TJ J Mol Cell Cardiol; 2016 Oct; 99():197-206. PubMed ID: 27620334 [TBL] [Abstract][Full Text] [Related]
9. Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia. Wolf CM; Moskowitz IP; Arno S; Branco DM; Semsarian C; Bernstein SA; Peterson M; Maida M; Morley GE; Fishman G; Berul CI; Seidman CE; Seidman JG Proc Natl Acad Sci U S A; 2005 Dec; 102(50):18123-8. PubMed ID: 16332958 [TBL] [Abstract][Full Text] [Related]
10. Sarcomere mutation negative hypertrophic cardiomyopathy is associated with ageing and obesity. de Feria AE; Kott AE; Becker JR Open Heart; 2021 Feb; 8(1):. PubMed ID: 33637569 [TBL] [Abstract][Full Text] [Related]
11. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. Kubo T; Gimeno JR; Bahl A; Steffensen U; Steffensen M; Osman E; Thaman R; Mogensen J; Elliott PM; Doi Y; McKenna WJ J Am Coll Cardiol; 2007 Jun; 49(25):2419-26. PubMed ID: 17599605 [TBL] [Abstract][Full Text] [Related]
12. Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy. de Marvao A; McGurk KA; Zheng SL; Thanaj M; Bai W; Duan J; Biffi C; Mazzarotto F; Statton B; Dawes TJW; Savioli N; Halliday BP; Xu X; Buchan RJ; Baksi AJ; Quinlan M; Tokarczuk P; Tayal U; Francis C; Whiffin N; Theotokis PI; Zhang X; Jang M; Berry A; Pantazis A; Barton PJR; Rueckert D; Prasad SK; Walsh R; Ho CY; Cook SA; Ware JS; O'Regan DP J Am Coll Cardiol; 2021 Sep; 78(11):1097-1110. PubMed ID: 34503678 [TBL] [Abstract][Full Text] [Related]
13. Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β. Teekakirikul P; Eminaga S; Toka O; Alcalai R; Wang L; Wakimoto H; Nayor M; Konno T; Gorham JM; Wolf CM; Kim JB; Schmitt JP; Molkentin JD; Norris RA; Tager AM; Hoffman SR; Markwald RR; Seidman CE; Seidman JG J Clin Invest; 2010 Oct; 120(10):3520-9. PubMed ID: 20811150 [TBL] [Abstract][Full Text] [Related]
14. Microstructural and Microvascular Phenotype of Sarcomere Mutation Carriers and Overt Hypertrophic Cardiomyopathy. Joy G; Kelly CI; Webber M; Pierce I; Teh I; McGrath L; Velazquez P; Hughes RK; Kotwal H; Das A; Chan F; Bakalakos A; Lorenzini M; Savvatis K; Mohiddin SA; Macfarlane PW; Orini M; Manisty C; Kellman P; Davies RH; Lambiase PD; Nguyen C; Schneider JE; Tome M; Captur G; Dall'Armellina E; Moon JC; Lopes LR Circulation; 2023 Sep; 148(10):808-818. PubMed ID: 37463608 [TBL] [Abstract][Full Text] [Related]
15. Differential contributions of sarcomere and mitochondria-related multigene variants to the endophenotype of hypertrophic cardiomyopathy. Chung H; Kim Y; Cho SM; Lee HJ; Park CH; Kim JY; Lee SH; Min PK; Yoon YW; Lee BK; Kim WS; Hong BK; Kim TH; Rim SJ; Kwon HM; Choi EY; Lee KA Mitochondrion; 2020 Jul; 53():48-56. PubMed ID: 32380161 [TBL] [Abstract][Full Text] [Related]
16. Unraveling the Genotype-Phenotype Relationship in Hypertrophic Cardiomyopathy: Obesity-Related Cardiac Defects as a Major Disease Modifier. Nollet EE; Westenbrink BD; de Boer RA; Kuster DWD; van der Velden J J Am Heart Assoc; 2020 Nov; 9(22):e018641. PubMed ID: 33174505 [TBL] [Abstract][Full Text] [Related]
17. Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy. Marian AJ; Braunwald E Circ Res; 2017 Sep; 121(7):749-770. PubMed ID: 28912181 [TBL] [Abstract][Full Text] [Related]
18. Ultrasonic Assessment of Myocardial Microstructure in Hypertrophic Cardiomyopathy Sarcomere Mutation Carriers With and Without Left Ventricular Hypertrophy. Hiremath P; Lawler PR; Ho JE; Correia AW; Abbasi SA; Kwong RY; Jerosch-Herold M; Ho CY; Cheng S Circ Heart Fail; 2016 Sep; 9(9):. PubMed ID: 27623770 [TBL] [Abstract][Full Text] [Related]
19. Moving Beyond the Sarcomere to Explain Heterogeneity in Hypertrophic Cardiomyopathy: JACC Review Topic of the Week. Maron BJ; Maron MS; Maron BA; Loscalzo J J Am Coll Cardiol; 2019 Apr; 73(15):1978-1986. PubMed ID: 31000001 [TBL] [Abstract][Full Text] [Related]
20. Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy. Jääskeläinen P; Vangipurapu J; Raivo J; Kuulasmaa T; Heliö T; Aalto-Setälä K; Kaartinen M; Ilveskoski E; Vanninen S; Hämäläinen L; Melin J; Kokkonen J; Nieminen MS; ; Laakso M; Kuusisto J ESC Heart Fail; 2019 Apr; 6(2):436-445. PubMed ID: 30775854 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]