The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry

التفاصيل البيبلوغرافية
العنوان: The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry
المؤلفون: 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
المصدر: Paediatrics Publications
Journal of Neuromuscular Diseases
بيانات النشر: Scholarship@Western, 2021.
سنة النشر: 2021
مصطلحات موضوعية: 0301 basic medicine, Research Report, Adult, Male, Pediatrics, medicine.medical_specialty, Canada, Registry, Neuromuscular disease, Adolescent, Duchenne muscular dystrophy, Myotonic dystrophy, Muscular Atrophy, Spinal, 03 medical and health sciences, Young Adult, 0302 clinical medicine, medicine, Humans, Myotonic Dystrophy, Registries, Amyotrophic lateral sclerosis, Child, real-world evidence, Aged, Aged, 80 and over, business.industry, Amyotrophic Lateral Sclerosis, Infant, Spinal muscular atrophy, Middle Aged, medicine.disease, Natural history, Muscular Dystrophy, Duchenne, 030104 developmental biology, Clinical research, Neurology, Muscular Dystrophies, Limb-Girdle, natural history, Child, Preschool, Female, Neurology (clinical), business, 030217 neurology & neurosurgery, Limb-girdle muscular dystrophy
الوصف: 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 disease. Diagnosis and contact information are collected across all diseases and detailed prospective data is collected for 5 specific diseases: Amyotrophic Lateral Sclerosis (ALS), Duchenne Muscular Dystrophy (DMD), Myotonic Dystrophy (DM), Limb Girdle Muscular Dystrophy (LGMD), and Spinal Muscular Atrophy (SMA). Since 2010, the CNDR has registered 4306 patients (1154 pediatric and 3148 adult) with 91 different neuromuscular diagnoses and has facilitated 125 projects (73 academic, 3 not-for-profit, 3 government, and 46 commercial) using registry data. In conclusion, the CNDR is an effective and productive pan-neuromuscular registry that has successfully facilitated a substantial number of studies over the past 10 years.
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5225e12fc979e2aa3b4ca1e72fb59591Test
https://ir.lib.uwo.ca/context/paedpub/article/3596/viewcontent/jnd_8_jnd200538.pdfTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....5225e12fc979e2aa3b4ca1e72fb59591
قاعدة البيانات: OpenAIRE