Calcium Receptor Binding of Cisplatin and Terbium in Human Breast Tumor Cells after Hyperthermia by Canada, Robert G.

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Enhancement of cisplatin cytotoxicity by terbium in cisplatin-resistant MDA/CH human breast cancer cells by FULLER, T. L, CANADA, R. G

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The effects of terbium on the cellular accumulation of cisplatin in MDA-MB-231 human breast tumor cells by MACK, K. M, CANADA, R. G, ANDREWS, P. A

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Binding of terbium and cisplatin to C13 human ovarian cancer cells using time-resolved terbium luminescence by Canada, Robert G., Paltoo, Dina N.

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The effects of terbium on the accumulation of cisplatin in human ovarian cancer cells by Canada, Robert G., Andrews, Paul A., Mack, Kelly M., Haider, Adnan

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Terbium luminescence studies of binding of adriamycin and cisplatin to tumorigenic cells by Canada, Robert G.

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Synergism between dipyridamole and cisplatin in human breast cancer cells in vitro by Perussi, Janice R., Paltoo, Dina N., Toppin, Veronica A. L., Canada, Robert G.

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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care by Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.

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Fermi surface in the absence of a Fermi liquid in the Kondo insulator SmB6 by Hartstein, M., Toews, W. H., Hsu, Y.-T., Zeng, B., Chen, X., Hatnean, M. Ciomaga, Zhang, Q. R., Nakamura, S., Padgett, A. S., Rodway-Gant, G., Berk, J., Kingston, M. K., Zhang, G. H., Chan, M. K., Yamashita, S., Sakakibara, T., Takano, Y., Park, J.-H., Balicas, L., Harrison, N., Shitsevalova, N., Balakrishnan, G., Lonzarich, G. G., Hill, R. W., Sutherland, M., Sebastian, Suchitra E.

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Explaining the dynamics of the ultra-relativistic third Van Allen radiation belt by Mann, I. R., Ozeke, L. G., Murphy, K. R., Claudepierre, S. G., Turner, D. L., Baker, D. N., Rae, I. J., Kale, A., Milling, D. K., Boyd, A. J., Spence, H. E., Reeves, G. D., Singer, H. J., Dimitrakoudis, S., Daglis, I. A., Honary, F.

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MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement by Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.

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Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease by Lee, Richard G, Balasubramaniam, Shanti, Stentenbach, Maike, Kralj, Tom, McCubbin, Tim, Padman, Benjamin, Smith, Janine, Riley, Lisa G, Priyadarshi, Archana, Peng, Liuyu, Nuske, Madison R, Webster, Richard, Peacock, Ken, Roberts, Philip, Stark, Zornitza, Lemire, Gabrielle, Ito, Yoko A, Boycott, Kym M, Geraghty, Michael T, van Klinken, Jan Bert, Ferdinandusse, Sacha, Zhou, Ying, Walsh, Rebecca, Marcellin, Esteban, Thorburn, David R, Rosciolli, Tony, Fletcher, Janice, Rackham, Oliver, Vaz, Frédéric M, Reid, Gavin E, Filipovska, Aleksandra

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Open EFTs, IR effects & late-time resummations: systematic corrections in stochastic inflation by Burgess, C. P., Holman, R., Tasinato, G.

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Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing by Balci, T.B., Hartley, T., Xi, Y., Dyment, D.A., Beaulieu, C.L., Bernier, F.P., Dupuis, L., Horvath, G.A., Mendoza‐Londono, R., Prasad, C., Richer, J., Yang, X.‐R., Armour, C.M., Bareke, E., Fernandez, B.A., McMillan, H.J., Lamont, R.E., Majewski, J., Parboosingh, J.S., Prasad, A.N., Rupar, C.A., Schwartzentruber, J., Smith, A.C., Tétreault, M., Innes, A.M., Boycott, K.M.

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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome by Doherty, Dan, Chudley, Albert E., Coghlan, Gail, Ishak, Gisele E., Innes, A. Micheil, Lemire, Edmond G., Rogers, R. Curtis, Mhanni, Aizeddin A., Phelps, Ian G., Jones, Steven J.M., Zhan, Shing H., Fejes, Anthony P., Shahin, Hashem, Kanaan, Moien, Akay, Hatice, Tekin, Mustafa, Triggs-Raine, Barbara, Zelinski, Teresa

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Are medical comorbidities contributing to the use of opioid analgesics in patients with knee osteoarthritis? by King, L.K., Marshall, D.A., Jones, C.A., Woodhouse, L.J., Ravi, B., Faris, P.D., Hawker, G.A., Hawker, G.A., Marshall, D.A., Bohm, E., Dunbar, M.J., Faris, P., Allyson Jones, C., Noseworthy, T., Ravi, B., Woodhouse, L.

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Interleukin-1 Blockade Inhibits the Acute Inflammatory Response in Patients With ST-Segment-Elevation Myocardial Infarction by Abbate, Antonio, Trankle, Cory R, Buckley, Leo F, Lipinski, Michael J, Appleton, Darryn, Kadariya, Dinesh, Canada, Justin M, Carbone, Salvatore, Roberts, Charlotte S, Abouzaki, Nayef, Melchior, Ryan, Christopher, Sanah, Turlington, Jeremy, Mueller, George, Garnett, James, Thomas, Christopher, Markley, Roshanak, Wohlford, George F, Puckett, Laura, Medina de Chazal, Horacio, Chiabrando, Juan G, Bressi, Edoardo, Del Buono, Marco Giuseppe, Schatz, Aaron, Vo, Chau, Dixon, Dave L, Biondi-Zoccai, Giuseppe G, Kontos, Michael C, Van Tassell, Benjamin W

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Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia by Schuurs-Hoeijmakers, Janneke H.M., Geraghty, Michael T., Kamsteeg, Erik-Jan, Ben-Salem, Salma, de Bot, Susanne T., Nijhof, Bonnie, van de Vondervoort, Ilse I.G.M., van der Graaf, Marinette, Nobau, Anna Castells, Otte-Höller, Irene, Vermeer, Sascha, Smith, Amanda C., Humphreys, Peter, Schwartzentruber, Jeremy, Ali, Bassam R., Al-Yahyaee, Saeed A., Tariq, Said, Pramathan, Thachillath, Bayoumi, Riad, Kremer, Hubertus P.H., van de Warrenburg, Bart P., van den Akker, Willem M.R., Gilissen, Christian, Veltman, Joris A., Janssen, Irene M., Vulto-van Silfhout, Anneke T., van der Velde-Visser, Saskia, Lefeber, Dirk J., Diekstra, Adinda, Erasmus, Corrie E., Willemsen, Michèl A., Vissers, Lisenka E.L.M., Lammens, Martin, van Bokhoven, Hans, Brunner, Han G., Wevers, Ron A., Schenck, Annette, Al-Gazali, Lihadh, de Vries, Bert B.A., de Brouwer, Arjan P.M.

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Hypertension Canada's 2017 Guidelines for Diagnosis, Risk Assessment, Prevention, and Treatment of Hypertension in Adults by Leung, Alexander A., MD, MPH, Daskalopoulou, Stella S., MD, PhD, Dasgupta, Kaberi, MD, MSc, McBrien, Kerry, MD, MPH, Butalia, Sonia, BSc, MD, Zarnke, Kelly B., MD, MSc, Nerenberg, Kara, MD, MSc, Harris, Kevin C., MD, MHSc, Nakhla, Meranda, MD, MSc, Cloutier, Lyne, RN, PhD, Gelfer, Mark, MD, Lamarre-Cliche, Maxime, MD, Milot, Alain, MD, MSc, MD, Bolli, Peter, MD, Tremblay, Guy, MD, McLean, Donna, RN, NP, PhD, Tobe, Sheldon W., MD, MSc(HPTE), Ruzicka, Marcel, MD, PhD, Burns, Kevin D., MD, Vallée, Michel, MD, PhD, Prasad, G.V. Ramesh, MBBS, MSc, Gryn, Steven E., MD, Feldman, Ross D., MD, Selby, Peter, MBBS, MHSc, Pipe, Andrew, CM, MD, Schiffrin, Ernesto L., MD, PhD, McFarlane, Philip A., MD, PhD, Oh, Paul, MD, Hegele, Robert A., MD, Khara, Milan, MBChB, Wilson, Thomas W., MD, Penner, S. Brian, MD, Burgess, Ellen, MD, Sivapalan, Praveena, MD, Herman, Robert J., MD, Bacon, Simon L., PhD, Rabkin, Simon W., MD, Gilbert, Richard E., MD, PhD, Campbell, Tavis S., PhD, Grover, Steven, MD, MPA, Honos, George, MD, Lindsay, Patrice, RN, PhD, Hill, Michael D., MD, MSc, Coutts, Shelagh B., MD, Gubitz, Gord, MD, Campbell, Norman R.C., MD, Moe, Gordon W., MD, MSc, Howlett, Jonathan G., MD, Boulanger, Jean-Martin, MD, Prebtani, Ally, MD, Kline, Gregory, MD, Leiter, Lawrence A., MD, Jones, Charlotte, MD, PhD, Côté, Anne-Marie, MD, MHSc, Woo, Vincent, MD, Kaczorowski, Janusz, PhD, Trudeau, Luc, MD, Tsuyuki, Ross T., BSc (Pharm), PharmD, MSc, Hiremath, Swapnil, MD, MPH, Drouin, Denis, MD, Lavoie, Kim L., PhD, Hamet, Pavel, MD, PhD, Grégoire, Jean C., MD, Lewanczuk, Richard, MD, PhD, Dresser, George K., MD, PhD, Sharma, Mukul, MD, MSc, Reid, Debra, PhD, DtP, Lear, Scott A., PhD, Moullec, Gregory, PhD, Gupta, Milan, MD, Magee, Laura A., MD, MSc, Logan, Alexander G., MD, Dionne, Janis, MD, Fournier, Anne, MD, Benoit, Geneviève, MD, Feber, Janusz, MD, Poirier, Luc, BPharm, MSc, Padwal, Raj S., MD, MSc, Rabi, Doreen M., MD, MSc

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Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families by Hartley, T., Wagner, J.D., Warman‐Chardon, J., Tétreault, M., Brady, L., Baker, S., Tarnopolsky, M., Bourque, P.R., Parboosingh, J.S., Smith, C., McInnes, B., Innes, A.M., Bernier, F., Curry, C.J., Yoon, G., Horvath, G.A., Bareke, E., Gillespie, M., Majewski, J., Bulman, D.E., Dyment, D.A., Boycott, K.M.

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