Why Does Influenza-Like Illness Surveillance Miss True Influenza Cases in the Emergency Department?: Implications for Health Care Providers by Rumoro, D.P, Hallock, M.M, Silva, J, Shah, S.C, Gibbs, G, Trenholme, G.M, Waddell, M.J

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17: The Impact of Specific Surveillance System Methodology on Influenza-Like Illness Prevalence Rates by Rumoro, D.P, Shah, S.C, Gibbs, G.S, Silva, J.C, Bayram, J.D, Hallock, M.M, Waddell, M.J

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Influence of the bonder on the adhesion of porcelain to machined titanium as determined by the strain energy release rate by Tholey, M.J, Waddell, J.N, Swain, M.V

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Combined lung-liver-pancreas transplantation in a recipient with cystic fibrosis by Barbas, A.S., Dib, M.J., Al-Adra, D.P., Goldaracena, N., Sapisochin, G., Waddell, T.K., Keshavjee, S., Selzner, N., Chaparro, C., Cattral, M.S.

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532 Glucose-6-phosphate Dehydrogenase Inhibition and Its Effects On the Radiosensitization of Head and Neck Squamous Carcinoma Cells by Hopkins, G.V, James, D.I, Cockerill, M.J, Small, H.F, Waddell, I.D, Ogilvie, D.J

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Identifying and assessing infectious disease risks to the health of the Canadian population by Garner, M.J, Pinault, L, LaBossiere, F, Anderson, C, Waddell, J. Trumble

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O.18 Systematic identification of causal mutations in Mendelian disorders using exome sequence data by Lek, M, Clarke, N.F, Waddell, L, Thomas, B, DePristo, M, Daly, M.J, North, K.N, MacArthur, D.G

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G.P.219 by Ghaoui, R, Corbett, A, Needham, M, Farrar, M, Sampaio, H, Mowat, D, Rajagopalan, S, Liang, C, Kaur, S, Waddell, L, Daly, K, Thomas, B.P, Lek, M, Daly, M.J, North, K.N, MacArthur, D.G, Sue, C.M, Clarke, N.F

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Overview of Microbial Food Safety Programs in Beef, Pork, and Poultry from Farm to Processing in Canada by Rajic, A, Waddell, L.A, Sargeant, J.M, Read, S, Farber, J, Firth, M.J, Chambers, A

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Reliability, Validity, and Responsiveness of the Western Ontario and McMaster Universities Osteoarthritis Index for Elderly Patients with a Femoral Neck Fracture by Bhandari, Mohit, Devereaux, P.J, McKay, Paula, Avram, Victoria, Williams, Dale, Duffy, Paul, Coady, Catherine, Glazebrook, Mark, Oxner, William, Reardon, Gerald, Wong, Ivan, Malo, Michel, Roy, Alain G, Lavigne, Martin, Danielwicz, Rebecca, Mont, Michael, Kapadia, Bhaveen, Bradbury, Thomas, Frizzell, Valda, Ringler, James R, Walker, Jane E, Kanlic, Enes, Manson, Maria, Jones, Neil, Alavekios, Damon, Colin, Vincent, Lopez, Gregory, Rothberg, David, van Jonbergen, Hans-Peter W, Barnaart, Alexander F.W, Steenstra, Ferry, ten Holder, Edgar J.T, van der Heide, Huub J.L, Keizer, Stefan B, Simons, Maarten P, van Bommel, Frank, Albers, G.H Rob, Doig, Stephen, Gong, Andrew, Young, Ian, Page, Richard, Beattie, Sally, Hjorthaug, Geir, Walter, Stephen, Zhou, Qi, Oatt, Amber, Buckley, Richard E, Lawendy, Abdel, Yee, Albert, Whelan, Daniel B, Coady, Cathy, Wood, Gavin, Howells, Fiona, Ward, Angela, Wai, Eugene K, Kingwell, Stephen P, Borsella, Vivian, Nastoff, Lauren A, Switzer, Julie A, Marston, Scott B, Kain, Michael S.H, Gross, Jonathan M, McIntyre, Allison W, Davis, Craig A, Lieberman, Shane, Finn, Erin, Karges, David, Luther, Arlene, Charlton, Michael, Parr, J Andrew, Gissel, Hannah, Lawson, Deanna, Linehan, Colleen, Roper, Elizabeth, Obremskey, William, Kregor, Philip, Hammacher, Eric R, de Vries, Mark R, Bosma, Jan, van Kampen, Albert, Liem, Ronald, Den Hartog, Dennis, van Wessem, Karlijn, Bhatia, Mahesh, Arora, Vinod, Subash, Yadav, Vineet, Singh, Sanjay, Lewis, Sophie, Anand, Sanjeev, Eke, Kate, Etherington, Greg, Halliday, Brett, Flynn, Annette, Ianssen, Torben, Borch, Tor, Jomaas, Geir, Kibsgård, Thomas, Lona, Tarjei, Smedsrud, Morten

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G.P.219: Diagnosing the limb-girdle muscular dystrophies using whole exome sequencing: An Australian cohort by Ghaoui, R., Corbett, A., Needham, M., Farrar, M., Sampaio, H., Mowat, D., Rajagopalan, S., Liang, C., Kaur, S., Waddell, L., Daly, K., Thomas, B.P., Lek, M., Daly, M.J., North, K.N., MacArthur, D.G., Sue, C.M., Clarke, N.F.

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G.O.2 by Kreissl, M, Sandaradura, S.A, Dowling, J.J, Kostyukova, A.S, Moroz, N, Quinlan, K.G, Lehtokari, V, Ravenscroft, G, Todd, E.J, Ceyhan-Birsoy, O, Gokhin, D.S, Maluenda, J, Lek, M, Nolent, F, Pappas, C.T, Novak, S.M, D’Amico, A, Malfatti, E, Thomas, B.P, Gabriel, S.B, Gupta, N, Daly, M.J, Ilkovski, B, Houweling, P.J, Swanson, L.C, Brownstein, C.A, Gupta, V.A, Medne, L, Shannon, P, Flisberg, A, Holmberg, E, den Bergh, P. Van, Lapunzina, P, Waddell, L.B, Sloboda, D.D, Bertini, E, Chitayat, D, Telfer, W.R, Laquerrière, A, Gregorio, C.C, Ottenheijm, C.A.C, Bönnemann, C.G, Pelin, K, Beggs, A.H, Hayashi, Y.K, Romero, N.B, Laing, N.G, Nishino, I, Wallgren-Pettersson, C, Melki, J, Fowler, V.M, MacArthur, D.G, North, K.N, Clarke, N.F

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G.O.2: Mutations in LMOD3 cause severe nemaline myopathy by disrupting thin filament organisation in skeletal muscle by Kreissl, M., Sandaradura, S.A., Dowling, J.J., Kostyukova, A.S., Moroz, N., Quinlan, K.G., Lehtokari, V., Ravenscroft, G., Todd, E.J., Ceyhan-Birsoy, O., Gokhin, D.S., Maluenda, J., Lek, M., Nolent, F., Pappas, C.T., Novak, S.M., D’Amico, A., Malfatti, E., Thomas, B.P., Gabriel, S.B., Gupta, N., Daly, M.J., Ilkovski, B., Houweling, P.J., Swanson, L.C., Brownstein, C.A., Gupta, V.A., Medne, L., Shannon, P., Flisberg, A., Holmberg, E., den Bergh, P. Van, Lapunzina, P., Waddell, L.B., Sloboda, D.D., Bertini, E., Chitayat, D., Telfer, W.R., Laquerrière, A., Gregorio, C.C., Ottenheijm, C.A.C., Bönnemann, C.G., Pelin, K., Beggs, A.H., Hayashi, Y.K., Romero, N.B., Laing, N.G., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V.M., MacArthur, D.G., North, K.N., Clarke, N.F.

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