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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy by Roberts, JD, Murphy, NP, Hamilton, RM, Lubbers, ER, James, CA, Kline, CF, Gollob, MH, Krahn, AD, Sturm, AC, Musa, H, El-Refaey, M, Koenig, S, Aneq, MÅ, Hoorntje, ET, Graw, SL, Davies, RW, Rafiq, MA, Koopmann, TT, Aafaqi, S, Fatah, M, Chiasson, DA, Taylor, MRG, Simmons, SL, Han, M, Van Opbergen, CJM, Wold, LE, Sinagra, G, Mittal, K, Tichnell, C, Murray, B, Codima, A, Nazer, B, Nguyen, DT, Marcus, FI, Sobriera, N, Lodder, EM, Van Den Berg, MP, Spears, DA, Robinson, JF, Ursell, PC, Green, AK, Skanes, AC, Tang, AS, Gardner, MJ, Hegele, RA, Van Veen, TAB, Wilde, AAM, Healey, JS, Janssen, PML, Mestroni, L, Van Tintelen, JP, Calkins, H, Judge, DP, Hund, TJ, Scheinman, MM, Mohler, PJ
Published 2019Journal article -
2
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect by Tadros, R, Francis, C, Xu, X, Vermeer, AMC, Harper, AR, Huurman, R, Kelu Bisabu, K, Walsh, R, Hoorntje, ET, Te Rijdt, WP, Buchan, RJ, van Velzen, HG, van Slegtenhorst, MA, Vermeulen, JM, Offerhaus, JA, Bai, W, de Marvao, A, Lahrouchi, N, Beekman, L, Karper, JC, Veldink, JH, Kayvanpour, E, Pantazis, A, Baksi, AJ, Whiffin, N, Mazzarotto, F, Sloane, G, Suzuki, H, Schneider-Luftman, D, Elliott, P, Richard, P, Ader, F, Villard, E, Lichtner, P, Meitinger, T, Tanck, MWT, van Tintelen, JP, Thain, A, McCarty, D, Hegele, RA, Roberts, JD, Amyot, J, Dubé, M-P, Cadrin-Tourigny, J, Giraldeau, G, L'Allier, PL, Garceau, P, Tardif, J-C, Boekholdt, SM, Lumbers, RT, Watkins, H
Published 2021Journal article