Biblio

Found 8 results
Filters: Author is Sanatani, S  [Clear All Filters]
2017
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.