Myofibrillar Myopathy Mimicking Polyneuropathy

por Bourque, Pierre R., Breiner, Ari, Warman-Chardon, Jodi
Publicado 2020

Paraneoplastic recurrent tumefactive demyelination in a 62-year-old man with metastatic seminoma

por Thebault, Simon, Hanes, Ilana, Woulfe, John, Bourque, Pierre R.
Publicado 2018

Causes of albuminocytological dissociation and the impact of age-adjusted cerebrospinal fluid protein reference intervals: a retrospective chart review of 2627 samples collected at...

por Brooks, John Alexander, McCudden, Christopher, Breiner, Ari, Bourque, Pierre R
Publicado 2019

Supramaximal Stimulus Intensity as a Diagnostic Tool in Chronic Demyelinating Neuropathy

por Parker, Vivien, Warman Chardon, Jodi, Mills, Julie, Goldsmith, Claire, Bourque, Pierre R.
Publicado 2016

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

por Bourque, Pierre R., Sampaio, Marcos Loreto, Warman-Chardon, Jodi, Samaan, Sam, Torres, Carlos
Publicado 2019

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

por Bourque, Pierre R., Brooks, John, McCudden, Christopher R., Warman-Chardon, Jodi, Breiner, Ari
Publicado 2019

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

por Bourque, Pierre R., Brooks, John, Mobach, Theo, Gammon, Brendan, Papp, Steven, Warman-Chardon, Jodi
Publicado 2020

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

por Bourque, Pierre R., Brooks, John, Mobach, Theo, Gammon, Braden, Papp, Steven, Warman-Chardon, Jodi
Publicado 2020

Isolated Internuclear Ophthalmoplegia as an Embolic Complication of Transcatheter Aortic Valve Implantation

por Thebault, Simon, Warman-Chardon, Jodi, O'Connell, Kathleen, Miller, William D, Bourque, Pierre R
Publicado 2022

Dataset for worldwide survey of cerebrospinal total protein upper reference values

por Bourque, Pierre R., Brooks, John, Warman-Chardon, Jodi, Hegen, Harald, Deisenhammer, Florian, McCudden, Chris R., Breiner, Ari
Publicado 2019

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

por Bourque, Pierre R., Warman-Chardon, Jodi, Lelli, Daniel A., LaBerge, Lauren, Kirshen, Carly, Bradshaw, Scott H., Hartley, Taila, Boycott, Kym M.
Publicado 2018

Case Report: Severe Peripartum Cardiac Disease in Myotonic Dystrophy Type 1

por Besant, Georgia, Bourque, Pierre R., Smith, Ian C., Chih, Sharon, Lamacie, Mariana M., Breiner, Ari, Zwicker, Jocelyn, Lochmüller, Hanns, Warman-Chardon, Jodi
Publicado 2022

Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy

por Smith, Ian C., Pileggi, Chantal A., Wang, Ying, Kernohan, Kristin, Hartley, Taila, McMillan, Hugh J., Sampaio, Marcos Loreto, Melkus, Gerd, Woulfe, John, Parmar, Gaganvir, Bourque, Pierre R., Breiner, Ari, Zwicker, Jocelyn, Pringle, C. Elizabeth, Jarinova, Olga, Lochmüller, Hanns, Dyment, David A., Brais, Bernard, Boycott, Kym M., Hekimi, Siegfried, Harper, Mary-Ellen, Warman-Chardon, Jodi
Publicado 2023