Neuropathological characterization of the cavitating leukoencephalopathy caused by COA8 cytochrome c oxidase deficiency: a case report von Chapleau, Alexandra, Boucher, Renée-Myriam, Pastinen, Tomi, Thiffault, Isabelle, Gould, Peter V., Bernard, Geneviève

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Risk of Guillain-Barré Syndrome Following H1N1 Influenza Vaccination in Quebec von De Wals, Philippe, Deceuninck, Geneviève, Toth, Eveline, Boulianne, Nicole, Brunet, Denis, Boucher, Renée-Myriam, Landry, Monique, De Serres, Gaston

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The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study von Yazdani, Pouneh Amir, St-Jean, Marie-Lou, Matovic, Sara, Spahr, Aaron, Tran, Luan T., Boucher, Renée-Myriam, Poulin, Chantal, Osterman, Bradley, Srour, Myriam, Rosenblatt, Bernard, Chénier, Sébastien, Soucy, Jean-Francois, Laberge, Anne-Marie, D’Agostino, Maria Daniela, Nguyen, Cam-Tu Emilie, Morsa, Maxime, Bernard, Geneviève

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Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic von Amir Yazdani, Pouneh, St-Jean, Marie-Lou, Matovic, Sara, Spahr, Aaron, Tran, Luan T., Boucher, Renée-Myriam, Poulin, Chantal, Osterman, Bradley, Srour, Myriam, Rosenblatt, Bernard, Chenier, Sébastien, Soucy, Jean-Francois, Laberge, Anne-Marie, Braverman, Nancy, D’Agostino, Maria Daniela, Nguyen, Cam-Tu Emilie, Morsa, Maxime, Bernard, Geneviève

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HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec von Waters, Paula J., Lace, Baiba, Buhas, Daniela, Gravel, Serge, Cyr, Denis, Boucher, Renée‐Myriam, Bernard, Geneviève, Lévesque, Sébastien, Maranda, Bruno

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Health-Related Quality of Life for Patients With Genetically Determined Leukoencephalopathy von Mirchi, Amytice, Pelletier, Félixe, Tran, Luan T., Keller, Stephanie, Braverman, Nancy, Tonduti, Davide, Vanderver, Adeline, Pizzino, Amy, Dilenge, Marie-Emmanuelle, Poulin, Chantal, Shevell, Michael, Majnemer, Annette, Sébire, Guillaume, Srour, Myriam, Osterman, Bradley, Boucher, Renée-Myriam, Vanasse, Michel, Rossignol, Elsa, Mitchell, John, Venkateswaran, Sunita, Pohl, Daniela, Kauffman, Marcelo, Schiffmann, Raphael, Goizet, Cyril, Moutton, Sebastien, Roncarolo, Federico, Bernard, Geneviève

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Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: α-glucosaminide N-acetyltransferase (HGSNAT) gene von Feldhammer, Matthew, Durand, Stéphanie, Mrázová, Lenka, Boucher, Renée-Myriam, Laframboise, Rachel, Steinfeld, Robert, Wraith, James E, Michelakakis, Helen, van Diggelen, Otto P, Hřebíček, Martin, Kmoch, Stanislav, Pshezhetsky, Alexey V

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Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 von Srour, Myriam, Hamdan, Fadi F., McKnight, Dianalee, Davis, Erica, Mandel, Hanna, Schwartzentruber, Jeremy, Martin, Brissa, Patry, Lysanne, Nassif, Christina, Dionne-Laporte, Alexandre, Ospina, Luis H., Lemyre, Emmanuelle, Massicotte, Christine, Laframboise, Rachel, Maranda, Bruno, Labuda, Damian, Décarie, Jean-Claude, Rypens, Françoise, Goldsher, Dorith, Fallet-Bianco, Catherine, Soucy, Jean-François, Laberge, Anne-Marie, Maftei, Catalina, Boycott, Kym, Brais, Bernard, Boucher, Renée-Myriam, Rouleau, Guy A., Katsanis, Nicholas, Majewski, Jacek, Elpeleg, Orly, Kukolich, Mary K., Shalev, Stavit, Michaud, Jacques L.

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Risk of Guillain-Barré Syndrome following Serogroup C Meningococcal Conjugate Vaccine in Quebec, Canada von De Wals, Philippe, Deceuninck, Geneviève, Boucher, Renée-Myriam, Ouakki, Manale

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Stable isotope evidence (Fe, Cu) suggests that sex, but not aging is recorded in rhesus macaque (Macaca mulatta) bone von Boucher, Renee D., Alavi, Shauhin E., Jong, Hylke N., Godfrey, Linda V., Vogel, Erin R.

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Strontium isotopes track female dispersal in Taï chimpanzees von Boucher, Renee D., Wittig, Roman M., Lemoine, Sylvain R. T., Maro, Aleksey, Wang, Xueye, Koch, Paul L., Oelze, Vicky M.

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A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay von Mucha, Bettina E., Banka, Siddharth, Ajeawung, Norbert Fonya, Molidperee, Sirinart, Chen, Gary G., Koenig, Mary Kay, Adejumo, Rhamat B., Till, Marianne, Harbord, Michael, Perrier, Renee, Lemyre, Emmanuelle, Boucher, Renee-Myriam, Skotko, Brian G., Waxler, Jessica L., Thomas, Mary Ann, Hodge, Jennelle C., Gecz, Jozef, Nicholl, Jillian, McGregor, Lesley, Linden, Tobias, Sisodiya, Sanjay M., Sanlaville, Damien, Cheung, Sau W., Ernst, Carl, Campeau, Philippe M.

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Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay von Mucha, Bettina E., Banka, Siddharth, Ajeawung, Norbert Fonya, Molidperee, Sirinart, Chen, Gary G., Koenig, Mary Kay, Adejumo, Rhamat B., Till, Marianne, Harbord, Michael, Perrier, Renee, Lemyre, Emmanuelle, Boucher, Renee-Myriam, Skotko, Brian G., Waxler, Jessica L., Thomas, Mary Ann, Hodge, Jennelle C., Gecz, Jozef, Nicholl, Jillian, McGregor, Lesley, Linden, Tobias, Sisodiya, Sanjay M., Sanlaville, Damien, Cheung, Sau W., Ernst, Carl, Campeau, Philippe M.

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Strontium isoscape of sub-Saharan Africa allows tracing origins of victims of the transatlantic slave trade von Wang, Xueye, Bocksberger, Gaëlle, Arandjelovic, Mimi, Agbor, Anthony, Angedakin, Samuel, Aubert, Floris, Ayimisin, Emmanuel Ayuk, Barubiyo, Donatienne, Bessone, Mattia, Bobe, René, Boucher, Renée, Brazzola, Gregory, Brewer, Simon, Lee, Kevin C., Carvalho, Susana, Chancellor, Rebecca, Cipoletta, Chloe, Cohen, Heather, Copeland, Sandi R., Costa, Ana Maria, Coupland, Charlotte, Curran, Bryan, Deschner, Tobias, Dieguez, Paula, Dierks, Karsten, Dilambaka, Emmanuel, Dowd, Dervla, Dunn, Andrew, Egbe, Villard Ebot, Finckh, Manfred, Gijanto, Liza, Yuh, Yisa Ginath, Goedmakers, Annemarie, Gokee, Cameron, Gomes Coelho, Rui, Goodman, Alan H., Granjon, Anne-Céline, Grimes, Vaughan, Grueter, Cyril C., Haour, Anne, Hedwig, Daniela, Hermans, Veerle, Hernandez-Aguilar, R. Adriana, Hohmann, Gottfried, Imong, Inaoyom, Jeffery, Kathryn J., Junker, Jessica, Kadam, Parag, Kambere, Mbangi, Kienast, Ivonne, Knudson, Kelly J., Langergraber, Kevin E., Lapeyre, Vincent, Lapuente, Juan, Larson, Bradley, Lautenschläger, Thea, le Roux, Petrus, Leinert, Vera, Logan, Amanda, Lowry, Brynn, Lüdecke, Tina, Maretti, Giovanna, Marrocoli, Sergio, Fernandez, Rumen, McNeill, Patricia J., Meier, Amelia C., Meller, Paulina, Monroe, J. Cameron, Morgan, David, Murai, Mizuki, Nicholl, Sonia, Niyigaba, Protais, Normand, Emmanuelle, Ormsby, Lucy Jayne, Pacheco, Liliana, Preece, Jodie, Regnaut, Sebastien, Richard, Francois G., Richards, Michael P., Rundus, Aaron, Sanz, Crickette, Sommer, Volker, Sponheimer, Matt, Steele, Teresa E., Stewart, Fiona A., Tagg, Nikki, Tédonzong, Luc Roscelin, Tickle, Alexander, Toubga, Lassané, Vergnes, Virginie, Njomen, Nadege Wangue, Wessling, Erin G., Willie, Jacob, Wittig, Roman M., Yurkiw, Kyle, Zipkin, Andrew M., Zuberbühler, Klaus, Kühl, Hjalmar S., Boesch, Christophe, Oelze, Vicky M.

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Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-old von Benabu, Yves, Beland, Mathieu, Ferguson, Natasha, Maranda, Bruno, Boucher, Renee-Myriam

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Peer-learning to employable : learnings from an evaluation of PASS attendee and facilitator perceptions of employability at Western Sydney University von Carr, Robert A, Evans-Locke, Kylie, Abu-Saif, Hanan, Boucher, Renee, Douglas, Karen

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Raising the Bar With Analytics von Kiron, David, Prentice, Pamela Kirk, Ferguson, Renee Boucher

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High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies von Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzeniecka, Sylvia, Meloche, Caroline, Retterer, Kyle, Cho, Megan T., Rosenfeld, Jill A., Bi, Weimin, Massicotte, Christine, Miguet, Marguerite, Brunga, Ledia, Regan, Brigid M., Mo, Kelly, Tam, Cory, Hollingsworth, Georgie, FitzPatrick, David R., Canham, Natalie, Blair, Edward, Kerr, Bronwyn, Fry, Andrew E., Thomas, Rhys H., Shelagh, Joss, Hurst, Jane A., Brittain, Helen, Blyth, Moira, Lebel, Robert Roger, Gerkes, Erica H., Davis-Keppen, Laura, Stein, Quinn, Dorison, Sara J., Benke, Paul J., Fassi, Emily, Corsten-Janssen, Nicole, Kamsteeg, Erik-Jan, Mau-Them, Frederic T., Bruel, Ange-Line, Verloes, Alain, Õunap, Katrin, Wojcik, Monica H., Albert, Dara V.F., Venkateswaran, Sunita, Ware, Tyson, Liu, Yu-Chi, Mohammad, Shekeeb S., Bizargity, Peyman, Bacino, Carlos A., Leuzzi, Vincenzo, Martinelli, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Blumkin, Lubov, Wierenga, Klaas J., Purcarin, Gabriela, O’Byrne, James J., Stockler, Sylvia, Lehman, Anna, Keren, Boris, Nougues, Marie-Christine, Mignot, Cyril, Auvin, Stéphane, Nava, Caroline, Hiatt, Susan M., Bebin, Martina, Shao, Yunru, Scaglia, Fernando, Frye, Richard E., Jarjour, Imad T., Jacques, Stéphanie, Boucher, Renee-Myriam, Riou, Emilie, Srour, Myriam, Carmant, Lionel, Lortie, Anne, Major, Philippe, Diadori, Paola, Dubeau, François, D’Anjou, Guy, Bourque, Guillaume, Berkovic, Samuel F., Sadleir, Lynette G., Campeau, Philippe M., Kibar, Zoha, Lafrenière, Ronald G., Girard, Simon L., Mercimek-Mahmutoglu, Saadet, Boelman, Cyrus, Rouleau, Guy A., Scheffer, Ingrid E., Mefford, Heather C., Andrade, Danielle M., Rossignol, Elsa, Minassian, Berge A., Michaud, Jacques L.

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Crafting Health Care's Future at Kaiser Permanente von Ferguson, Renee Boucher

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A New, Analytics-Based Era of Banking Dawns at State Street von Ferguson, Renee Boucher

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