Ketogenic diet for mitochondrial disease: potential role in treating the Multiple Symmetric Lipomatosis phenotype associated with the common MT-TK genetic mutation

por Mattman, Andre, Nadeau, Elizabeth, Mezei, Michelle M., Cresswell, Mark, Zhao, Sida, Bosdet, Taryn, Sin, Don D., Guenette, Jordan A., Dupuis, Isabelle, Allin, Emily, Clarke, David C.
Publicado 2022

Response from Authors to the Letter to the Editor

por Appendino, Juan Pablo, Baker, Steven, Chapman, Kristine M., Dykstra, Tamara, Hussein, Tabrez, Jones, Michelle-Lee, Mezei, Michelle M., Mirsattari, Seyed M., Ng, Marcus, Nikkel, Joanne, Obradovic, Vaso, Phan, Cecile, Robinson, Lawrence, Scott, Angela, Téllez-Zenteno, José, Van Niekerk, Michelle, Venance, Shannon, Moore, Fraser
Publicado 2021

Practice Guidelines for Canadian Neurophysiology Laboratories During the COVID-19 Pandemic

por Appendino, Juan Pablo, Baker, Steven K., Chapman, Kristine M., Dykstra, Tamara, Hussein, Tabrez, Jones, Michelle-Lee, Mezei, Michelle M., Mirsattari, Seyed M., Ng, Marcus, Nikkel, Joanne, Obradovic, Vaso, Phan, Cecile, Robinson, Lawrence, Scott, Angela, Tellez-Zenteno, Jose, Van Niekerk, Michelle, Venance, Shannon, Moore, Fraser
Publicado 2020

Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis

por Harlalka, Gaurav V., Lehman, Anna, Chioza, Barry, Baple, Emma L., Maroofian, Reza, Cross, Harold, Sreekantan-Nair, Ajith, Priestman, David A., Al-Turki, Saeed, McEntagart, Meriel E., Proukakis, Christos, Royle, Louise, Kozak, Radoslaw P., Bastaki, Laila, Patton, Michael, Wagner, Karin, Coblentz, Roselyn, Price, Joy, Mezei, Michelle, Schlade-Bartusiak, Kamilla, Platt, Frances M., Hurles, Matthew E., Crosby, Andrew H.
Publicado 2013

Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America

por Green, Joshua D, Barohn, Richard J, Bartoccion, Emanuela, Benatar, Michael, Blackmore, Derrick, Chaudhry, Vinay, Chopra, Manisha, Corse, Andrea, Dimachkie, Mazen M, Evoli, Amelia, Florence, Julaine, Freimer, Miriam, Howard, James F, Jiwa, Theresa, Kaminski, Henry J, Kissel, John T, Koopman, Wilma J, Lipscomb, Bernadette, Maestri, Michelanglo, Marino, Mariapaola, Massey, Janice M, McVey, April, Mezei, Michelle M, Muppidi, Srikanth, Nicolle, Michael W, Oger, Joel, Pascuzzi, Robert M, Pasnoor, Mamatha, Pestronk, Alan, Provenzano, Carlo, Ricciardi, Roberta, Richman, David P, Rowin, Julie, Sanders, Donald B, Siddiqi, Zaeem, Soloway, Aimee, Wolfe, Gil I, Wulf, Charlie, Drachman, Daniel B, Traynor, Bryan J
Publicado 2020

A National Spinal Muscular Atrophy Registry for Real-World Evidence

por Hodgkinson, Victoria L., Oskoui, Maryam, Lounsberry, Joshua, M’Dahoma, Saïd, Butler, Emily, Campbell, Craig, MacKenzie, Alex, McMillan, Hugh J., Simard, Louise, Vajsar, Jiri, Brais, Bernard, Chapman, Kristine M., Chrestian, Nicolas, Crone, Meghan, Dobrowolski, Peter, Dojeiji, Susan, Dowling, James J., Dupré, Nicolas, Genge, Angela, Gonorazky, Hernan, Hasal, Simona, Izenberg, Aaron, Johnston, Wendy, Leung, Edward, Lochmüller, Hanns, Mah, Jean K., Marerro, Alier, Massie, Rami, McAdam, Laura, McCormick, Anna, Melanson, Michel, Mezei, Michelle M., Nguyen, Cam-Tu E., O’Connell, Colleen, O’Ferrall, Erin K., Pfeffer, Gerald, Phan, Cecile, Plamondon, Stephanie, Poulin, Chantal, Rodrigue, Xavier, Schellenberg, Kerri L., Selby, Kathy, Sheriko, Jordan, Shoesmith, Christen, Smith, Garth, Taillon, Monique, Taylor, Sean, Warman Chardon, Jodi, Worley, Scott, Korngut, Lawrence
Publicado 2020