A crucial first randomized controlled trial of thymectomy in non-thymomatous myasthenia gravis

Tekijä Bourque, Pierre R., Warman Chardon, Jodi
Julkaisussa J Thorac Dis (2016)

Myofibrillar Myopathy Mimicking Polyneuropathy

Tekijä Bourque, Pierre R., Breiner, Ari, Warman-Chardon, Jodi
Julkaisussa Case Rep Neurol (2020)

Supramaximal Stimulus Intensity as a Diagnostic Tool in Chronic Demyelinating Neuropathy

Tekijä Parker, Vivien, Warman Chardon, Jodi, Mills, Julie, Goldsmith, Claire, Bourque, Pierre R.
Julkaisussa Neurosci J (2016)

Neurolymphomatosis of the lumbosacral plexus and its branches: case series and literature review

Tekijä Bourque, Pierre R., Sampaio, Marcos Loreto, Warman-Chardon, Jodi, Samaan, Sam, Torres, Carlos
Julkaisussa BMC Cancer (2019)

The Added Value of Cardiac Magnetic Resonance in Muscular Dystrophies

Tekijä Lamacie, Mariana M., Warman-Chardon, Jodi, Crean, Andrew M., Florian, Anca, Wahbi, Karim
Julkaisussa J Neuromuscul Dis (2019)

Age matters: Impact of data-driven CSF protein upper reference limits in Guillain-Barré syndrome

Tekijä Bourque, Pierre R., Brooks, John, McCudden, Christopher R., Warman-Chardon, Jodi, Breiner, Ari
Julkaisussa Neurol Neuroimmunol Neuroinflamm (2019)

Systematic prospective electrophysiological studies of the median nerve after simple distal radius fracture

Tekijä Bourque, Pierre R., Brooks, John, Mobach, Theo, Gammon, Brendan, Papp, Steven, Warman-Chardon, Jodi
Julkaisussa PLoS One (2020)

Correction: Systematic prospective electrophysiological studies of the median nerve after simple distal radius fracture

Tekijä Bourque, Pierre R., Brooks, John, Mobach, Theo, Gammon, Braden, Papp, Steven, Warman-Chardon, Jodi
Julkaisussa PLoS One (2020)

Dataset for worldwide survey of cerebrospinal total protein upper reference values

Tekijä Bourque, Pierre R., Brooks, John, Warman-Chardon, Jodi, Hegen, Harald, Deisenhammer, Florian, McCudden, Chris R., Breiner, Ari
Julkaisussa Data Brief (2019)

The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome

Tekijä McDonell, Laura M, Warman Chardon, Jodi, Schwartzentruber, Jeremy, Foster, Denise, Beaulieu, Chandree L, Majewski, Jacek, Bulman, Dennis E, Boycott, Kym M
Julkaistu 2014

Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy

Tekijä Kernohan, Kristin D., Cigana Schenkel, Laila, Huang, Lijia, Smith, Amanda, Pare, Guillaume, Ainsworth, Peter, Boycott, Kym M., Warman-Chardon, Jodi, Sadikovic, Bekim
Julkaisussa Clin Epigenetics (2016)

Novel ELOVL4 mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)

Tekijä Bourque, Pierre R., Warman-Chardon, Jodi, Lelli, Daniel A., LaBerge, Lauren, Kirshen, Carly, Bradshaw, Scott H., Hartley, Taila, Boycott, Kym M.
Julkaisussa Neurol Genet (2018)

Survival Motor Neuron Protein is Released from Cells in Exosomes: A Potential Biomarker for Spinal Muscular Atrophy

Tekijä Nash, Leslie A., McFall, Emily R., Perozzo, Amanda M., Turner, Maddison, Poulin, Kathy L., De Repentigny, Yves, Burns, Joseph K., McMillan, Hugh J., Warman Chardon, Jodi, Burger, Dylan, Kothary, Rashmi, Parks, Robin J.
Julkaisussa Sci Rep (2017)

Clinical and genetic study of hereditary spastic paraplegia in Canada

Tekijä Chrestian, Nicolas, Dupré, Nicolas, Gan-Or, Ziv, Szuto, Anna, Chen, Shiyi, Venkitachalam, Anil, Brisson, Jean-Denis, Warman-Chardon, Jodi, Ahmed, Sohnee, Ashtiani, Setareh, MacDonald, Heather, Mohsin, Noreen, Mourabit-Amari, Karim, Provencher, Pierre, Boycott, Kym M., Stavropoulos, Dimitri J., Dion, Patrick A., Ray, Peter N., Suchowersky, Oksana, Rouleau, Guy A., Yoon, Grace
Julkaisussa Neurol Genet (2016)

Abnormal fatty acid metabolism is a core component of spinal muscular atrophy

Tekijä Deguise, Marc‐Olivier, Baranello, Giovanni, Mastella, Chiara, Beauvais, Ariane, Michaud, Jean, Leone, Alessandro, De Amicis, Ramona, Battezzati, Alberto, Dunham, Christopher, Selby, Kathryn, Warman Chardon, Jodi, McMillan, Hugh J., Huang, Yu‐Ting, Courtney, Natalie L., Mole, Alannah J., Kubinski, Sabrina, Claus, Peter, Murray, Lyndsay M., Bowerman, Melissa, Gillingwater, Thomas H., Bertoli, Simona, Parson, Simon H., Kothary, Rashmi
Julkaisussa Ann Clin Transl Neurol (2019)

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

Tekijä Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba‐Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D., Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E. C., Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J. R., Wood, Nicholas W., Rothman, James E., Boycott, Kym M., Mills, Philippa B., Clayton, Peter T., Houlden, Henry
Julkaisussa Ann Neurol (2019)

A National Spinal Muscular Atrophy Registry for Real-World Evidence

Tekijä 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
Julkaisussa Can J Neurol Sci (2020)