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Pierre R Bourque

Showing results (51-60 of 67) with videos related to

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The Lancet. Neurology|May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy developmentRachel Thompson, Sally Spendiff, Andreas Roos, et al.
Muscle & Nerve|October 8, 2019
Impact of disuse muscular atrophy on the compound muscle action potentialTheo Mobach, John Brooks, Ari Breiner, et al.
Journal of Neuromuscular Diseases|February 19, 2025
Current biomarkers in inclusion body myositisEden Daniel, Ian C Smith, Marcos L Sampaio, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 26, 2018
Intraneural Ganglion Cysts of the Fibular Nerve: A Cause of Fluctuating Painful Foot DropPierre R Bourque, Kirsty U Boyd, Gerard H Jansen, et al.
Neurology. Genetics|August 2, 2018
Novel <i>ELOVL4</i> mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)Pierre R Bourque, Jodi Warman-Chardon, Daniel A Lelli, et al.
Plos One|July 26, 2024
Direct and indirect costs of idiopathic inflammatory myopathies in adults: A systematic reviewEden Daniel, Ian C Smith, Valentina Ly, et al.
Frontiers in Cardiovascular Medicine|June 20, 2022
Case Report: Severe Peripartum Cardiac Disease in Myotonic Dystrophy Type 1Georgia Besant, Pierre R Bourque, Ian C Smith, et al.
Neuromuscular Disorders : NMD|November 5, 2023
Emerging and established biomarkers of oculopharyngeal muscular dystrophyIan C Smith, Shaoni Chakraborty, Pierre R Bourque, et al.
Neuromuscular Disorders : NMD|December 3, 2022
Quantitative vs qualitative muscle MRI: Imaging biomarker in patients with Oculopharyngeal Muscular Dystrophy (OPMD)Gerd Melkus, Marcos L Sampaio, Ian C Smith, et al.
Annals of Clinical and Translational Neurology|December 31, 2024
Refractory myasthenia gravis treated with autologous hematopoietic stem cell transplantationBenjamin Beland, Jan Storek, Liam Quartermain, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
The Lancet. Neurology|May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy developmentRachel Thompson, Sally Spendiff, Andreas Roos, et al.
Muscle & Nerve|October 8, 2019
Impact of disuse muscular atrophy on the compound muscle action potentialTheo Mobach, John Brooks, Ari Breiner, et al.
Journal of Neuromuscular Diseases|February 19, 2025
Current biomarkers in inclusion body myositisEden Daniel, Ian C Smith, Marcos L Sampaio, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|July 26, 2018
Intraneural Ganglion Cysts of the Fibular Nerve: A Cause of Fluctuating Painful Foot DropPierre R Bourque, Kirsty U Boyd, Gerard H Jansen, et al.
Neurology. Genetics|August 2, 2018
Novel <i>ELOVL4</i> mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)Pierre R Bourque, Jodi Warman-Chardon, Daniel A Lelli, et al.
Plos One|July 26, 2024
Direct and indirect costs of idiopathic inflammatory myopathies in adults: A systematic reviewEden Daniel, Ian C Smith, Valentina Ly, et al.
Frontiers in Cardiovascular Medicine|June 20, 2022
Case Report: Severe Peripartum Cardiac Disease in Myotonic Dystrophy Type 1Georgia Besant, Pierre R Bourque, Ian C Smith, et al.
Neuromuscular Disorders : NMD|November 5, 2023
Emerging and established biomarkers of oculopharyngeal muscular dystrophyIan C Smith, Shaoni Chakraborty, Pierre R Bourque, et al.
Neuromuscular Disorders : NMD|December 3, 2022
Quantitative vs qualitative muscle MRI: Imaging biomarker in patients with Oculopharyngeal Muscular Dystrophy (OPMD)Gerd Melkus, Marcos L Sampaio, Ian C Smith, et al.
Annals of Clinical and Translational Neurology|December 31, 2024
Refractory myasthenia gravis treated with autologous hematopoietic stem cell transplantationBenjamin Beland, Jan Storek, Liam Quartermain, et al.
Pageof 7