Found 8 results
Filters: Author is Sanatani, S  [Clear All Filters]
M. Abdelsayed, Baruteau, A. E., Gibbs, K., Sanatani, S., Krahn, A. D., Probst, V., and Ruben, P. C., Differential calcium sensitivity in NaV 1.5 mixed syndrome mutants, Journal of Physiology, vol. 595, no. 18, pp. 6165-6186, 2017.
G. Mellor, Laksman, Z. W. M., Tadros, R., Roberts, J. D., Gerull, B., Simpson, C. S., Klein, G. J., Champagne, J., Talajic, M., Gardner, M., Steinberg, C., Arbour, L., Birnie, D. H., Angaran, P., Leather, R., Sanatani, S., Chauhan, V. S., Seifer, C., Healey, J. S., and Krahn, A. D., Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry), Circulation: Cardiovascular Genetics, vol. 10, no. 3, p. pii: e001686, 2017.
J. D. Roberts, Krah, A. D., Ackerman, M. J., Rohatgi, R. K., Moss, A. J., Nazer, B., Tadros, R., Gerull, B., Sanatani, S., Wijeyeratne, Y. D., Baruteau, A. E., Muir, A. R., Pang, B., Cadrin-Tourigny, J., Talajic, M., Rivard, L., Tester, D. J., Liu, T., Whitman, I. R., Wojciak, J., Conacher, S., Gula, L. J., Leong-Sit, P., Manlucu, J., Green, M. S., Hamilton, R., Healey, J. S., Lopes, C. M., Behr, E. R., Wilde, A. A., Gollob, M. H., and Scheinman, M. M., Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?, Circulation: Arrhythmia and Electrophysiology, vol. 10, no. 8, p. e005282, 2017.
T. M. Roston, Guo, W., Krahn, A. D., Wang, R., Van Petegem, F., Sanatani, S., ,, and Lehman, A., A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardia, J Electrocardiol., vol. 50, no. 2, 2017.