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824 results

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Page 1
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants.
Kozek K, Wada Y, Sala L, Denjoy I, Egly C, O'Neill MJ, Aiba T, Shimizu W, Makita N, Ishikawa T, Crotti L, Spazzolini C, Kotta MC, Dagradi F, Castelletti S, Pedrazzini M, Gnecchi M, Leenhardt A, Salem JE, Ohno S, Zuo Y, Glazer AM, Mosley JD, Roden DM, Knollmann BC, Blume JD, Extramiana F, Schwartz PJ, Horie M, Kroncke BM. Kozek K, et al. Among authors: roden dm. Circ Genom Precis Med. 2021 Aug;14(4):e003289. doi: 10.1161/CIRCGEN.120.003289. Epub 2021 Jul 26. Circ Genom Precis Med. 2021. PMID: 34309407 Free PMC article.
Genetics of acquired long QT syndrome.
Roden DM, Viswanathan PC. Roden DM, et al. J Clin Invest. 2005 Aug;115(8):2025-32. doi: 10.1172/JCI25539. J Clin Invest. 2005. PMID: 16075043 Free PMC article. Review.
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: roden dm. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes.
Mohler PJ, Le Scouarnec S, Denjoy I, Lowe JS, Guicheney P, Caron L, Driskell IM, Schott JJ, Norris K, Leenhardt A, Kim RB, Escande D, Roden DM. Mohler PJ, et al. Among authors: roden dm. Circulation. 2007 Jan 30;115(4):432-41. doi: 10.1161/CIRCULATIONAHA.106.656512. Epub 2007 Jan 22. Circulation. 2007. PMID: 17242276
Clinical practice. Long-QT syndrome.
Roden DM. Roden DM. N Engl J Med. 2008 Jan 10;358(2):169-76. doi: 10.1056/NEJMcp0706513. N Engl J Med. 2008. PMID: 18184962 Review. No abstract available.
824 results