Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Xavier Rodrigue"'
Autor:
Isabelle Lessard, Isabelle Côté, Raphaël St-Gelais, Luc J. Hébert, Bernard Brais, Jean Mathieu, Xavier Rodrigue, Cynthia Gagnon
Publikováno v:
The Cerebellum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d03829c2b1c993105f4715a8c49791a1
https://doi.org/10.1007/s12311-023-01558-w
https://doi.org/10.1007/s12311-023-01558-w
Autor:
Aasef G. Shaikh, Ji-Soo Kim, Caroline Froment, Yu Jin Koo, Nicolas Dupre, Marios Hadjivassiliou, Jerome Honnorat, Sudhir Kothari, Hiroshi Mitoma, Xavier Rodrigue, Jeremy Schmahmann, Bing-Wen Soong, S. H. Subramony, Michael Strupp, Mario Manto
Publikováno v:
Contemporary Clinical Neuroscience ISBN: 9783031243448
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f53824cc5a0411279d7796e180a7940c
https://doi.org/10.1007/978-3-031-24345-5_11
https://doi.org/10.1007/978-3-031-24345-5_11
Autor:
Monique Taillon, Jeremy Slayter, Angela Genge, Kristine M. Chapman, Hanns Lochmüller, Christen Shoesmith, Aaron Izenberg, Wendy Johnston, Christine Stables, Colleen O'Connell, Stephanie Plamondon, Jodi Warman-Chardon, Lawrence Korngut, Victoria Hodgkinson, Kerri Schellenberg, Bernard Brais, Erin K. O'Ferrall, Gerald Pfeffer, Josh Lounsberry, Xavier Rodrigue
Publikováno v:
Journal of Neuromuscular Diseases
Background: Spinal Muscular Atrophy (SMA) is a rare disease that affects 1 in 11 000 live births. Recent developments in SMA treatments have included new disease-modifying therapies that require high quality data to inform decisions around initiation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a8c69bfeac82753b239ff91fd5fe43
https://doi.org/10.3233/jnd-200617
https://doi.org/10.3233/jnd-200617
Autor:
Aasef G. Shaikh, Ji-Soo Kim, Caroline Froment, Yu Jin Koo, Nicolas Dupre, Marios Hadjivassiliou, Jerome Honnorat, Sudhir Kothari, Hiroshi Mitoma, Xavier Rodrigue, Bing-Wen Soong, S.H. Subramony, Michael Strupp, Jeremy Schmahmann, Mario Manto
Publikováno v:
Journal of the neurological sciences. 443
Eye movements are fundamental diagnostic and progression markers of various neurological diseases, including those affecting the cerebellum. Despite the high prevalence of abnormal eye movements in patients with cerebellar disorders, the traditional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89388172bd323cf998a2ff0961cfbac4
https://pubmed.ncbi.nlm.nih.gov/36403298
https://pubmed.ncbi.nlm.nih.gov/36403298
Autor:
Laura McAdam, James J. Dowling, Monique Taillon, Anna McCormick, Said M’dahoma, Gerald Pfeffer, Cam-Tu Emilie Nguyen, Colleen O'Connell, Craig Campbell, Scott Worley, Hernan Gonorazky, Alex MacKenzie, Aaron Izenberg, Jiri Vajsar, Peter Dobrowolski, Emily Butler, Jean K. Mah, Simona Hasal, Alier Marerro, Hugh J. McMillan, Garth Smith, Erin K. O'Ferrall, Hanns Lochmüller, Michelle M. Mezei, Christen Shoesmith, Nicolas Dupré, Victoria Hodgkinson, Nicolas Chrestian, Louise R. Simard, Meghan Crone, Cecile Phan, Jodi Warman Chardon, Xavier Rodrigue, Jordan Sheriko, Michel Melanson, Kathy Selby, Angela Genge, Edward Leung, Maryam Oskoui, Kristine M. Chapman, Stephanie Plamondon, Kerri Schellenberg, Rami Massie, Bernard Brais, Joshua J. Lounsberry, Susan Dojeiji, Sean W. Taylor, Wendy Johnston, Chantal Poulin, Lawrence Korngut
Publikováno v:
Paediatrics Publications
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
Background:Spinal muscular atrophy (SMA) is a devastating rare disease that affects individuals regardless of ethnicity, gender, and age. The first-approved disease-modifying therapy for SMA, nusinursen, was approved by Health Canada, as well as by A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcd6223874661f3ecd05a30e16b4ebad
https://doi.org/10.1017/cjn.2020.111
https://doi.org/10.1017/cjn.2020.111
Autor:
Tim Benstead, Hernan Gonorazky, C. Krieger, Victoria Hodgkinson, Said M’dahoma, E. Leung, Aaron Izenberg, Angela Russell, Gerald Pfeffer, Kristine M. Chapman, A. Marrero, James J. Dowling, H. Briemberg, Monique Taillon, Lorne Zinman, Nicolas Chrestian, Angela Genge, Nicolas Dupré, Simona Hasal, Agessandro Abrahao, G. Matte, S. Dojeiji, Shannon L. Venance, C. Campbell, S. Botez, Hans D. Katzberg, R.G. Smith, Maryam Oskoui, Erin K. O'Ferrall, Alex MacKenzie, I. Grant, G. Linassi, Colleen O'Connell, P.R. Bourque, J. K. Mah, Xavier Rodrigue, Scott Worley, Michel Melanson, S. Taylor, Anna McCormick, Kerri Schellenberg, Laura McAdam, Christen Shoesmith, Stephanie Plamondon, Joshua J. Lounsberry, C. Phan, Kathy Selby, Rami Massie, M. Crone, H. McMillan, Bernard Brais, G. Jewett, Peter Dobrowolski, Jordan Sheriko, Wendy Johnston, Jodi Warman-Chardon, Lawrence Korngut, Neil R. Cashman, S. Kalra, Hanns Lochmüller, Michelle M. Mezei, C. T. Nguyen, Chantal Poulin
Publikováno v:
Paediatrics Publications
Journal of Neuromuscular Diseases
Journal of Neuromuscular Diseases
We report the recruitment activities and outcomes of a multi-disease neuromuscular patient registry in Canada. The Canadian Neuromuscular Disease Registry (CNDR) registers individuals across Canada with a confirmed diagnosis of a neuromuscular diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5225e12fc979e2aa3b4ca1e72fb59591
https://ir.lib.uwo.ca/context/paedpub/article/3596/viewcontent/jnd_8_jnd200538.pdf
https://ir.lib.uwo.ca/context/paedpub/article/3596/viewcontent/jnd_8_jnd200538.pdf
Autor:
François Routhier, Xavier Rodrigue, Krista L Best, Luc J. Hébert, Cynthia Gagnon, Julie Bourassa, Caroline Rahn, Raphaël St-Gelais, Bernard Brais
Publikováno v:
Disability and rehabilitation. Assistive technology.
Although approximately 45% of adults with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) are permanent wheelchair users, this sub population has been less studied. The purpose of this study was to document wheelchair mobility, mot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2f990613bb5e0cb35f0360ea78803b
https://pubmed.ncbi.nlm.nih.gov/33307884
https://pubmed.ncbi.nlm.nih.gov/33307884
Autor:
Maryam Oskoui, Aaron Izenberg, Xavier Rodrigue, Kerri Schellenberg, Gerald Pfeffer, Lawrence Korngut, Victoria Hodgkinson, Stephanie Plamondon, Colleen O'Connell, Bernard Brais, Hanns Lochmüller, Jodi Warman-Chardon, Christen Shoesmith, Erin K. O'Ferrall, Kristine M. Chapman
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 48(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b26dde1d50d26eba8cd4031b2d163c5
https://pubmed.ncbi.nlm.nih.gov/32713403
https://pubmed.ncbi.nlm.nih.gov/32713403
Autor:
Maude-Marie Gagnon, Xavier Rodrigue, Mathieu Bélanger, Dax Bourcier, Jean-Denis Brisson, Jean Mathieu, Matthis Synofzik, Isabelle Côté, Bernard Brais, Cynthia Gagnon
Publikováno v:
Journal of the neurological sciences 417, 117050-(2020). doi:10.1016/j.jns.2020.117050
Background The Scale for the Assessment and Rating of Ataxia (SARA) is a commonly used scale measuring the severity of cerebellar ataxia and is a candidate for outcome measurement in foreseeable clinical trials in Autosomal Recessive Spastic Ataxia o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96e4e82cb97bc856b6ccdba7c64d8ad
https://pubmed.ncbi.nlm.nih.gov/32736199
https://pubmed.ncbi.nlm.nih.gov/32736199
Autor:
Marie-Michèle Briand, Isabelle Lessard, Cynthia Gagnon, Isabelle Côté, Jean Mathieu, Bernard Brais, Xavier Rodrigue
Publikováno v:
Journal of the Neurological Sciences. 400:39-41
Background and purpose Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) diagnosis is based on the presence of three main clinical features: 1) ataxia, 2) pyramidal involvement, and 3) axonal neuropathy. This study aimed to explore,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d13cc557d8d2306386658fedf7a356
https://doi.org/10.1016/j.jns.2019.03.008
https://doi.org/10.1016/j.jns.2019.03.008