Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Pierre R. Bourque"'
Autor:
Georgia Besant, Pierre R. Bourque, Ian C. Smith, Sharon Chih, Mariana M. Lamacie, Ari Breiner, Jocelyn Zwicker, Hanns Lochmüller, Jodi Warman-Chardon
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
BackgroundMyotonic dystrophy type 1 (DM1) is a hereditary muscular dystrophy affecting ∼2.1–14.3/100,000 adults. Cardiac manifestations of DM1 include conduction disorders and rarely cardiomyopathies. DM1 increases the risk of obstetric complicat
Externí odkaz:
https://doaj.org/article/c924dd416f3144719f4c5306bed38fa4
Publikováno v:
Case Reports in Neurology, Vol 12, Iss 1, Pp 97-102 (2020)
A 76-year-old man with a 5-year history of gait difficulties was suspected to have length-dependent sensorimotor polyneuropathy. Electrodiagnostic results pointed to a foot drop of neurogenic etiology, except for the prominence of myotonic discharges
Externí odkaz:
https://doaj.org/article/66deefe0c22e440d8fefd7c01d2795e8
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Neurolymphomatosis (NL) is a direct process of invasion of peripheral nerves by lymphoma. It occurs in roughly 5% of patients with lymphoma and represents a particularly difficult diagnostic dilemma when it is the presenting focal
Externí odkaz:
https://doaj.org/article/0ea7d47e5ffd46a89912c18fd8850d11
Autor:
Pierre R. Bourque, John Brooks, Jodi Warman-Chardon, Harald Hegen, Florian Deisenhammer, Chris R. McCudden, Ari Breiner
Publikováno v:
Data in Brief, Vol 23, Iss , Pp - (2019)
This article reports data pertaining to a worldwide web-based survey referenced in the publication “Adult CSF Total Protein: Higher upper reference limits should be considered worldwide ” (P.R. Bourque, et al., 2019). This survey was distributed
Externí odkaz:
https://doaj.org/article/839a29edb3dd4e32a95c72663d1ed8a8
Autor:
Eden Daniel, Ian C Smith, Valentina Ly, Pierre R Bourque, Ari Breiner, Hanns Lochmuller, Nancy Maltez, Kednapa Thavorn, Jodi Warman-Chardon
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0307144 (2024)
Idiopathic inflammatory myopathies (IIMs) are rare disorders characterized by inflammation of skeletal muscle, which can result in fatty replacement of muscle, muscle atrophy, and subsequent weakness. Therapeutic advancements have improved clinical o
Externí odkaz:
https://doaj.org/article/266d83ae99954a3f8100eebece3b8649
Autor:
Ari Breiner, Emilie Lalonde, Jocelyn Zwicker, Ryan Daniel Gotesman, Douglas A McKim, Jodi Warman-Chardon, Pierre R. Bourque
Publikováno v:
Muscle & Nerve. 65:400-404
Introduction Laryngospasm is an involuntary sustained closure of sphincter musculature that leads to an unpleasant subjective experience of dyspnea and choking. It is an underreported symptom in amyotrophic lateral sclerosis (ALS). This study aimed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0add22d407c131bd2f0420abc0235df0
https://doi.org/10.1002/mus.27466
https://doi.org/10.1002/mus.27466
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45dc49095fb63b0b184502f9199bb68c
https://doi.org/10.7759/cureus.32292
https://doi.org/10.7759/cureus.32292
Publikováno v:
Neurohospitalist
Background and Purpose: Elevation of total protein level in cerebrospinal fluid (CSF-TP) in diabetic patients is often disregarded by clinicians. However, existing studies on the topic have significant limitations, and therefore we aimed to explore t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324cb928463b9670cd442fda411ed3e9
https://doi.org/10.1177/19418744211039376
https://doi.org/10.1177/19418744211039376
Autor:
Ari Breiner, Kawan Rakhra, Simon Thebault, Hans Frykman, Jodi Warman-Chardon, Ebrima Gibbs, Pierre R. Bourque, Doug McKim
Publikováno v:
Neuromuscular Disorders. 31:1279-1281
Myasthenia gravis is a treatable autoimmune disease caused by autoantibodies directed against membrane proteins at the neuromuscular junction. While acetylcholine receptor antibodies are most common, a minority of patients have antibodies directed ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::508698a947f52a8a6aa82097ab978f8b
https://doi.org/10.1016/j.nmd.2021.08.014
https://doi.org/10.1016/j.nmd.2021.08.014
Autor:
Ari Breiner, Sultan Altouri, Harold L. Atkins, Lothar Huebsch, David S. Allan, Jodi Warman-Chardon, Catherine E. Pringle, Michael Lee Kennah, Pierre R. Bourque, Christopher Bredeson, Lisa Martin, Sheryl McDiarmid, Natasha Kekre, Josée Masson-Roy
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. :1-7
Background: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) refractory to conventional therapy can lead to marked disability and represents a therapeutic challenge. Objective: To report five cases of treatment-refractory disabling CI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c51589c556198fd5889f65f4791acac
https://doi.org/10.1017/cjn.2021.30
https://doi.org/10.1017/cjn.2021.30