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Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome.
Meier AB, Raj Murthi S, Rawat H, Toepfer CN, Santamaria G, Schmid M, Mastantuono E, Schwarzmayr T, Berutti R, Cleuziou J, Ewert P, Görlach A, Klingel K, Laugwitz KL, Seidman CE, Seidman JG, Moretti A, Wolf CM. Meier AB, et al. Among authors: seidman jg, seidman ce. iScience. 2021 Dec 9;25(1):103596. doi: 10.1016/j.isci.2021.103596. eCollection 2022 Jan 21. iScience. 2021. PMID: 34988410 Free PMC article.
Genetic causes of human heart failure.
Morita H, Seidman J, Seidman CE. Morita H, et al. J Clin Invest. 2005 Mar;115(3):518-26. doi: 10.1172/JCI24351. J Clin Invest. 2005. PMID: 15765133 Free PMC article. Review.
Cardiac myosin-binding protein-C phosphorylation and cardiac function.
Sadayappan S, Gulick J, Osinska H, Martin LA, Hahn HS, Dorn GW 2nd, Klevitsky R, Seidman CE, Seidman JG, Robbins J. Sadayappan S, et al. Among authors: seidman jg, seidman ce. Circ Res. 2005 Nov 25;97(11):1156-63. doi: 10.1161/01.RES.0000190605.79013.4d. Epub 2005 Oct 13. Circ Res. 2005. PMID: 16224063 Free PMC article.
Cardiovascular genomics.
Sabatine MS, Seidman JG, Seidman CE. Sabatine MS, et al. Among authors: seidman jg, seidman ce. Circulation. 2006 Mar 21;113(11):e450-5. doi: 10.1161/CIRCULATIONAHA.105.560151. Circulation. 2006. PMID: 16549641 No abstract available.
Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics.
Alcalai R, Seidman JG, Seidman CE. Alcalai R, et al. Among authors: seidman jg, seidman ce. J Cardiovasc Electrophysiol. 2008 Jan;19(1):104-10. doi: 10.1111/j.1540-8167.2007.00965.x. Epub 2007 Oct 4. J Cardiovasc Electrophysiol. 2008. PMID: 17916152 Review.
Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy.
Maron BJ, Roberts WC, Arad M, Haas TS, Spirito P, Wright GB, Almquist AK, Baffa JM, Saul JP, Ho CY, Seidman J, Seidman CE. Maron BJ, et al. JAMA. 2009 Mar 25;301(12):1253-9. doi: 10.1001/jama.2009.371. JAMA. 2009. PMID: 19318653 Free PMC article.
578 results