The role of sugammadex in the development and modification of an allergic response to rocuronium: evidence from a cutaneous model by Clarke, R. C., Sadleir, P. H. M., Platt, P. R.

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Efficacy of sugammadex in rocuronium‐induced or antibiotic‐induced anaphylaxis. A case–control study by Platt, P. R., Clarke, R. C., Johnson, G. H., Sadleir, P. H. M.

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Epinephrine (adrenaline) preventing recovery from intraoperative anaphylactic shock complicated by systolic anterior motion of the mitral valve with left ventricular outflow tract... by Sadleir, P. H. M., Clarke, R. C., Lim, B. S. L., Platt, P. R.

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Intraoperative anaphylaxis to sugammadex and a protocol for intradermal skin testing by Sadleir, P H M, Russell, T, Clarke, R C, Maycock, E, Platt, P R

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Consequences of proceeding with surgery after resuscitation from intra‐operative anaphylaxis by Sadleir, P. H. M., Clarke, R. C., Bozic, B., Platt, P. R.

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Sugammadex, rocuronium and mast cell numbers in the rat liver by Platt, P. R., Sadleir, P. H. M., Clarke, R. C.

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Adverse events in the removal of naltrexone implants by SADLEIR, P. H. M, GARDNER, A. I, HENNESSY, B

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Systemic mastocytosis presenting as intraoperative anaphylaxis with atypical features: a report of two cases by Bridgman, D E, Clarke, R, Sadleir, P H M, Stedmon, J J, Platt, P

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In reply to Baldo by Sadleir, P H M, Russell, T, Clarke, R C, Maycock, E, Platt, P R

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures by Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome by Heron, Sarah E., Grinton, Bronwyn E., Kivity, Sara, Afawi, Zaid, Zuberi, Sameer M., Hughes, James N., Pridmore, Clair, Hodgson, Bree L., Iona, Xenia, Sadleir, Lynette G., Pelekanos, James, Herlenius, Eric, Goldberg-Stern, Hadassa, Bassan, Haim, Haan, Eric, Korczyn, Amos D., Gardner, Alison E., Corbett, Mark A., Gécz, Jozef, Thomas, Paul Q., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies by Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study by Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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A Long-Snouted Predatory Dinosaur from Africa and the Evolution of Spinosaurids by Sereno, Paul C., Beck, Allison L., Dutheil, Didier B., Gado, Boubacar, Hans C. E. Larsson, Lyon, Gabrielle H., Marcot, Jonathan D., Oliver W. M. Rauhut, Sadleir, Rudyard W., Sidor, Christian A., Varricchio, David D., Wilson, Gregory P., Wilson, Jeffrey A.

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Josephson Effects in Frequency-Domain Multiplexed TES Microcalorimeters and Bolometers by Gottardi, L., Smith, S. J., Kozorezov, A., Akamatsu, H., van der Kuur, J., Bandler, S. R., Bruijn, M. P., Chervenak, J. A., Gao, J. R., den Hartog, R. H., Jackson, B. D., Khosropanah, P., Miniussi, A., Nagayoshi, K., Ridder, M., Sadleir, J., Sakai, K., Wakeham, N.

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Study of Dissipative Losses in AC-Biased Mo/Au Bilayer Transition-Edge Sensors by Sakai, K., Adams, J. S., Bandler, S. R., Chervenak, J. A., Datesman, A. M., Eckart, M. E., Finkbeiner, F. M., Kelley, R. L., Kilbourne, C. A., Miniussi, A. R., Porter, F. S., Sadleir, J. S., Smith, S. J., Wakeham, N. A., Wassell, E. J., Yoon, W., Akamatsu, H., Bruijn, M. P., Gottardi, L., Jackson, B. D., Kuur, J. van der, Leeuwen, B. J. van, Linden, A. J. van der, Weers, H. J. van, Kiviranta, M.

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study by Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Diverse genetic causes of polymicrogyria with epilepsy by Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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TES-Based X-Ray Microcalorimeter Performances Under AC Bias and FDM for Athena by Akamatsu, H., Gottardi, L., de Vries, C. P., Adams, J. S., Bandler, S. R., Bruijn, M. P., Chervenak, J. A., Eckart, M. E., Finkbeiner, F. M., Gao, J. R., den Herder, J.-W., den Hartog, R., Hoevers, H., Kelley, R. E., Khosropanah, P., Kilbourne, C. A., van der Kuur, J., Lee, S.-J., van den Linden, A. J., Porter, F. S., Ravensberg, K., Sadleir, J. E., Smith, S. J., Suzuki, T., Wassell, E. J., Kiviranta, M.

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Phenotypic analysis of 303 multiplex families with common epilepsies

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