1. Trang chủ
  2. » Kinh Tế - Quản Lý

Andersons pediatric cardiology 1669

3 3 0

Đang tải... (xem toàn văn)

THÔNG TIN TÀI LIỆU

85 Coppini R, Ferrantini C, Yao L, et al Late sodium current inhibition reverses electromechanical dysfunction in human hypertrophic cardiomyopathy Circulation 2013;127(5):575–584 86 Georgakopoulos D, Christe ME, Giewat M, et al The pathogenesis of familial hypertrophic cardiomyopathy: early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation Nat Med 1999;5(3):327–330 87 Alves ML, Gaffin RD, Wolska BM Rescue of familial cardiomyopathies by modifications at the level of sarcomere and ca2+ fluxes J Mol Cell Cardiol 2010;48(5):834–842 88 Fatkin D, McConnell BK, Mudd JO, et al An abnormal ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy J Clin Invest 2000;106(11):1351–1359 89 Coppini R, Mazzoni L, Ferrantini C, et al Ranolazine prevents phenotype development in a mouse model of hypertrophic cardiomyopathy Circ Heart Fail 2017;10(3) 90 Kohler J, Winkler G, Schulte I, et al Mutation of the myosin converter domain alters cross-bridge elasticity Proc Natl Acad Sci USA 2002;99(6):3557–3562 91 Spudich JA Hypertrophic and dilated cardiomyopathy: four decades of basic research on muscle lead to potential therapeutic approaches to these devastating genetic diseases Biophys J 2014;106(6):1236–1249 92 Spudich JA The myosin mesa and a possible unifying hypothesis for the molecular basis of human hypertrophic cardiomyopathy Biochem Soc Trans 2015;43(1):64–72 93 Crilley JG, Boehm EA, Blair E, et al Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy J Am Coll Cardiol 2003;41(10):1776–1782 94 Abozguia K, Elliott P, McKenna W, et al Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy Circulation 2010;122(16):1562–1569 95 Green EM, Wakimoto H, Anderson RL, et al A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice Science 2016;351(6273):617–621 96 Beadle RM, Williams LK, Kuehl M, et al Improvement in cardiac energetics by perhexiline in heart failure due to dilated cardiomyopathy JACC Heart Fail 2015;3(3):202–211 97 Ho CY, Lakdawala NK, Cirino AL, et al Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expression JACC Heart Fail 2015;3(2):180– 188 98 Olivotto I, Hellawell JL, Farzaneh-Far R, et al Novel approach targeting the complex pathophysiology of hypertrophic cardiomyopathy: the impact of late sodium current inhibition on exercise capacity in subjects with symptomatic hypertrophic cardiomyopathy (LIBERTY-HCM) trial Circ Heart Fail 2016;9(3):e002764 99 Ho CY, McMurray JJV, Cirino AL, et al The design of the valsartan for attenuating disease evolution in early sarcomeric hypertrophic cardiomyopathy (VANISH) trial Am Heart J 2017;187:145–155 100 Aoki Y, Niihori T, Kawame H, et al Germline mutations in HRAS proto-oncogene cause costello syndrome Nat Genet 2005;37(10):1038–1040 101 Burch M, Sharland M, Shinebourne E, et al

Ngày đăng: 22/10/2022, 12:39

Xem thêm: