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The TREAT-NMD duchenne muscular dystrophy registries: Conception, design, and utilization by industry and academia

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作者单位: University of Calgary, Health Sciences Centre, NW Calgary, AB, Canada [1] Turku University Central Hospital, Turku, Finland [2] Muskelcentrum, Dep of Neurology, US?, ?rebro, Sweden [3] Rublevskoe shosse, Moscow, Russian Federation [4] Department of Neurology, Warszawa Banacha 1a, Poland [5] Pediatric Neurology Department, Hospital Al. Obregia, Bucharest, Romania [6] Hospital Pediatría J. P. Garrahan, Argentina [7] Office of Population Health Genomics, Department of Health, 189 Royal Street, Level 3C WA, Australia [8] Istanbul University Faculty of Medicine, Neurology Department, PTR Unit, Istanbul, Turkey [9] Parent Project Onlus, Via Aurelia 1299 Roma, Italy [10] Clinic for Child Neurology and Psychiatry, Belgrade, Serbia [11] Centro de Genética Médica Jacinto Magalh?es, Porto, Portugal [12] Paediatric Neurology and Neurorehabilitation Unit, Lausanne University Hospital, Lausanne [13] University Medical Center, Freiburg, Germany [14] Institute for Biostatistics and Analyses, Masaryk University, Brno, Czech Republic [15] Hacettepe University Faculty of Health Sciences Department of Physiotherapy and Rehabilitation [16] Pasteur Institute of Iran, Karaj Complex, Tehran, Iran [17] Department of Paediatrics, Clinical Neurological Sciences and Epidemiology, Western University [18] National Danish Rehabilitation Centre for Neuromuscular Diseases, Aarhus, Denmark [19] INSERM UMR-S910, Aix-Marseille UniversitéFaculté de Médecine La Timone, Marseille Cedex, France [20] The Ohio State University, Nationwide Children's Hospital, Columbus, OH, United States [21] Department of Neurology, Medical University-Sofia, Sofia, Bulgaria [22] Leiden University Medical Center, Department of Neurology, Leiden, Netherlands [23] WIV-ISP, Brussels, Belgium [24] Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Munich [25] MRC Centre for Neuromuscular Diseases at Newcastle, Institute of Genetic Medicine, Newcastle upon [26] National Centre for Rare Diseases, Istituto Superiore di Sanità, Rome, Italy [27] Laboratoire de Biochimie et Génétique Moléculaire, H?pital Cochin, Paris, France [28] Translational Medical Centre, National Centre of Neurology and Psychiatry, 4-1-1 Ogawa-Higashi [29] Action Duchenne, Epicentre, London, United Kingdom [30] Division of Paediatric Neurology, University Hospital Centre Zagreb (KBC Zagreb), University of [31] NIEH, Molecular Genetic Department, Budapest, Hungary [32] Institute of Neurology, Psychiatry and Narcology of NAMS, Kharkiv, Ukraine [33] Kanchi Kamakoti CHILDS Trust Hospital, Nungambakkam, Chennai, India [34] Fondazione Telethon-Piazza Cavour 1, Milan, Italy [35] Institute of Rare Diseases Research, Institute of Health Carlos III, Madrid, Spain [36] Laboratoire de Génétique de Maladies Rares, Université Montpellier 1 and Inserm U827, Montpellier [37] Department of Neurology, Peking Union Medical College Hospital, Peking Union Medical College [38] Neurology, Auckland City Hospital, Auckland, New Zealand [39] DuchenneConnect, Hackensack, NJ, United States [40] Unit of Genetics, Hospital la Fe, Valencia, Spain [41]
发布时间 2018-09-20
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