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Long QT Syndrome: Genetics and Future Perspective.
Wallace E, Howard L, Liu M, O'Brien T, Ward D, Shen S, Prendiville T. Wallace E, et al. Among authors: prendiville t. Pediatr Cardiol. 2019 Oct;40(7):1419-1430. doi: 10.1007/s00246-019-02151-x. Epub 2019 Aug 22. Pediatr Cardiol. 2019. PMID: 31440766 Free PMC article. Review.
Heterotaxy syndrome: defining contemporary disease trends.
Prendiville TW, Barton LL, Thompson WR, Fink DL, Holmes KW. Prendiville TW, et al. Pediatr Cardiol. 2010 Oct;31(7):1052-8. doi: 10.1007/s00246-010-9764-z. Epub 2010 Aug 21. Pediatr Cardiol. 2010. PMID: 20730421
Generation of eight human induced pluripotent stem cell (iPSC) lines from familial Long QT Syndrome type 1 (LQT1) patients carrying KCNQ1 c.1697C>A mutation (NUIGi005-A, NUIGi005-B, NUIGi005-C, NUIGi006-A, NUIGi006-B, NUIGi006-C, NUIGi007-A, and NUIGi007-B).
Ge N, Liu M, Krawczyk J, McInerney V, Galvin J, Shen S, O'Brien T, Prendiville T. Ge N, et al. Among authors: prendiville t. Stem Cell Res. 2019 Aug;39:101502. doi: 10.1016/j.scr.2019.101502. Epub 2019 Jul 26. Stem Cell Res. 2019. PMID: 31415974 Free article.
49 results