Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Josiane Bourré‐Tessier"'
Autor:
Minoru Satoh, Océane Landon-Cardinal, Alexandra Albert, Sabrina Hoa, Jean-Luc Senecal, Martial Koenig, Josiane Bourré-Tessier, Eric Rich, Jean-Richard Goulet, Yves Troyanov, Hajar El Kamouni, Darya S. Jalaledin, Caroline Vo, Gemma Pérez, May Y. Choi, Marvin J. Fritzler
Publikováno v:
RMD Open, Vol 9, Iss 4 (2023)
Objectives The survival of motor neuron (SMN) complex has an essential role in the assembly of small nuclear ribonucleoproteins (RNP). Recent reports have described autoantibodies (aAbs) to the SMN complex as novel biomarkers in anti-U1RNP+ myositis
Externí odkaz:
https://doaj.org/article/32783c5c168c449fabb9c93409d6a0c7
Autor:
Flavie Roy, Pat Korathanakhun, Jason Karamchandani, Bruno-Pierre Dubé, Océane Landon-Cardinal, Nathalie Routhier, Caroline Peyronnard, Rami Massie, Valérie Leclair, Alain Meyer, Josiane Bourré-Tessier, Minoru Satoh, Marvin J. Fritzler, Jean-Luc Senécal, Marie Hudson, Erin K. O’Ferrall, Yves Troyanov, Benjamin Ellezam, Jean-Paul Makhzoum
Publikováno v:
BMC Rheumatology, Vol 6, Iss 1, Pp 1-6 (2022)
Abstract Background Shrinking lung syndrome (SLS) is a rare manifestation of systemic lupus erythematosus (SLE) characterized by decreased lung volumes and diaphragmatic weakness in a dyspneic patient. Chest wall dysfunction secondary to pleuritis is
Externí odkaz:
https://doaj.org/article/f886c995049f489cbf9c59e52bc6e0e4
Autor:
Alain Meyer, Yves Troyanov, Julie Drouin, Geneviève Oligny-Longpré, Océane Landon-Cardinal, Sabrina Hoa, Baptiste Hervier, Josiane Bourré-Tessier, Anne-Marie Mansour, Sara Hussein, Vincent Morin, Eric Rich, Jean-Richard Goulet, Sandra Chartrand, Marie Hudson, Jessica Nehme, Jean-Paul Makhzoum, Farah Zarka, Edith Villeneuve, Jean-Pierre Raynauld, Marianne Landry, Erin K. O’Ferrall, Jose Ferreira, Benjamin Ellezam, Jason Karamchandani, Sandrine Larue, Rami Massie, Catherine Isabelle, Isabelle Deschênes, Valérie Leclair, Hélène Couture, Ira N. Targoff, Marvin J. Fritzler, Jean-Luc Senécal
Publikováno v:
Arthritis Research & Therapy, Vol 22, Iss 1, Pp 1-10 (2020)
Abstract Objective To describe successful therapeutic strategies in statin-induced anti-HMGCR myopathy. Methods Retrospective data from a cohort of 55 patients with statin-induced anti-HMGCR myopathy, sequentially stratified by the presence of proxim
Externí odkaz:
https://doaj.org/article/7cd542ee442d4d3e8caaecafd505f1e6
Autor:
Darosa Lim, Océane Landon-Cardinal, Benjamin Ellezam, Annie Belisle, Annie Genois, Jennifer Sirois, Josiane Bourré-Tessier
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) immune-mediated necrotizing myopathy is a subtype of idiopathic inflammatory myopathy which may be associated with statin exposure. It presents with severe proximal muscle weakness, high cr
Externí odkaz:
https://doaj.org/article/386978e5c59146d38475e6b33a14d0aa
Autor:
Alain Meyer, Marvin J Fritzler, Minoru Satoh, Océane Landon-Cardinal, Marie Hudson, Valérie Leclair, Sabrina Hoa, Isabelle Richard, Jean-Luc Senecal, Martial Koenig, Alexandra Baril-Dionne, Josiane Bourré-Tessier, Anne-Marie Mansour, Farah Zarka, Jean-Paul Makhzoum, Jessica Nehme, Eric Rich, Jean-Richard Goulet, Tamara Grodzicky, France Joyal, Ira Targoff, Yves Troyanov
Publikováno v:
RMD Open, Vol 6, Iss 2 (2020)
Objective To describe systemic sclerosis (SSc) with myopathy in patients without classic SSc-specific and SSc-overlap autoantibodies (aAbs), referred to as seronegative scleromyositis.Methods Twenty patients with seronegative scleromyositis diagnosed
Externí odkaz:
https://doaj.org/article/176416c177604d4d8f52ad8c1cd59a07
Autor:
Alain Meyer, Yves Troyanov, Pat Korathanakhun, Océane Landon-Cardinal, Valérie Leclair, Hughes Allard-Chamard, Josiane Bourré-Tessier, Jean-Paul Makhzoum, Catherine Isabelle, Sandrine Larue, Francois Grand'Maison, Rami Massie, Matthieu Le Page, Anne-Marie Mansour, Nathalie Routhier, Farah Zarka, Flavie Roy, Joshua Sonnen, Minoru Satoh, Marvin Fritzler, Marie Hudson, Jean-Luc Senécal, Jason Karamchandani, Benjamin Ellezam, Erin O'Ferrall
Publikováno v:
Neuromuscular Disorders. 33:169-182
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0b45bdc51b0f38aace943f9d25f6343
https://doi.org/10.1016/j.nmd.2022.12.001
https://doi.org/10.1016/j.nmd.2022.12.001
Publikováno v:
The Journal of rheumatology. 50(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::886bf7a3f0c8e736b9b79c511ab73c0a
https://pubmed.ncbi.nlm.nih.gov/36109076
https://pubmed.ncbi.nlm.nih.gov/36109076
Autor:
Benjamin Ellezam, Valérie Leclair, Yves Troyanov, Imane Bersali, Margherita Giannini, Sabrina Hoa, Josiane Bourré‐Tessier, Valérie Nadon, Julie Drouin, Jason Karamchandani, Erin O'Ferrall, Béatrice Lannes, Minoru Satoh, Marvin J. Fritzler, Jean‐Luc Senécal, Marie Hudson, Alain Meyer, Océane Landon‐Cardinal
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 48(7)
We aim to perform ultrastructural and histopathological analysis of muscle biopsies from a large group of systemic sclerosis (SSc) patients, including some with early/mild SSc features, and examine whether capillary pathology differentiates 'scleromy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f01ce7727c4b9aafd5b7bbe674273d
https://pubmed.ncbi.nlm.nih.gov/35894636
https://pubmed.ncbi.nlm.nih.gov/35894636
Publikováno v:
Epileptic Disorders. 22:349-352
Porphyrias are rare genetic disorders which cause a deficiency in the enzymes involved in the biosynthesis of heme. The treatment of epilepsy in patients with acute intermittent porphyria can be difficult since many anticonvulsants can increase heme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f39c1b0fa095010235d9aa593c1d1c
https://doi.org/10.1684/epd.2020.1171
https://doi.org/10.1684/epd.2020.1171
Autor:
Océane Landon-Cardinal, Hugues Allard-Chamard, Hugo Chapdelaine, Stéphane Doucet, Éric Rich, Josiane Bourré-Tessier
Publikováno v:
Annals of the Rheumatic Diseases. :ard-2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf322c8cfda230c51a0b34f83cdd8b60
https://doi.org/10.1136/ard-2022-223541
https://doi.org/10.1136/ard-2022-223541