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14 p, 396.7 KB Assessment of disease progression in dysferlinopathy : A 1-year cohort study / Moore, U. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Jacobs, Marni (Pediatrics. Epidemiology and Biostatistics. George Washington University) ; James, M.K. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Mayhew, A.G. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Fernandez-Torron, R. (Neuromuscular Area. Biodonostia Health Research Institute. Neurology Service) ; Feng, J. (Center for Translational Science. Division of Biostatistics and Study Methodolog) ; Cnaan, A. (Pediatrics. Epidemiology and Biostatistics. GeorgeWashington University) ; Eagle, M. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Bettinson, K. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Rufibach, L.E. (Jain Foundation) ; Lofra, R.M. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Blamire, A.M. (Magnetic Resonance Centre. Institute of CellularMedicine. Newcastle University) ; Carlier, P.G. (AIM CEA NMR Laboratory. Institute ofMyology. Pitiacute;e-Salpcirc;etrigrave;ere University Hospital) ; Mittal, P. (Jain Foundation) ; Lowes, L.P. (Research Institute at Nationwide Childrens Hospital. TheOhio State University) ; Alfano, L. (Research Institute at Nationwide Childrens Hospital. TheOhio State University) ; Rose, K. (Institute for Neuroscience andMuscle Research. ChildrensHospital atWestmead. University of Sydney) ; Duong, T. (Lucile Salter Packard ChildrensHospital at Stanford) ; Berry, K.M. (Research Institute at Nationwide Childrens Hospital. TheOhio State University) ; Montiel-Morillo, E. (Institut d'Investigació Biomèdica Sant Pau) ; Pedrosa-Hernández, I. (Institut d'Investigació Biomèdica Sant Pau) ; Holsten, S. (Neuroscience Institute. Carolinas Neuromuscular/ALS-MDA Center. Carolinas HealthCare System) ; Sanjak, M. (Neuroscience Institute. Carolinas Neuromuscular/ALS-MDA Center. Carolinas HealthCare System) ; Ashida, A. (Department of Physical Rehabilitation. National Center Hospital. National Center of Neurology and Psychiatry) ; Sakamoto, C. (Department of Physical Rehabilitation. National Center Hospital. National Center of Neurology and Psychiatry) ; Tateishi, T. (Department of Physical Rehabilitation. National Center Hospital. National Center of Neurology and Psychiatry) ; Yajima, H. (Department of Physical Rehabilitation. National Center Hospital. National Center of Neurology and Psychiatry) ; Canal, A. (Institut deMyologie. AP-HP. GH Pitiacute;e-Salpcirc;etrigrave;ere) ; Ollivier, G. (Institut deMyologie. AP-HP. GH Pitiacute;e-Salpcirc;etrigrave;ere) ; Decostre, V. (Institut deMyologie. AP-HP. GH Pitiacute;e-Salpcirc;etrigrave;ere) ; Mendez, J.B. (Neurorehabilitation Unit. Rehabilitation Hospital Universitario Virgen del Rocacute;io Sevilla) ; Praxedes, N.S.A. (Neurophysiotherapy Department. Hospital Universitario Virgen del Rocacute;io) ; Thiele, S. (Friedrich-Baur-Institute. Department of Neurology. Ludwig-Maximilians-University of Munich) ; Siener, C. (Department of Neurology. Washington University School of Medicine) ; Shierbecker, J. (Department of Neurology. Washington University School of Medicine) ; Florence, J.M. (Cooperative International Neuromuscular Research Group. Department of Neurology) ; Vandevelde, B. (Centre de Reference des Maladies Neuromusculaires PACA Racute;eunion Rhone Alpes. Hopital de la Timone. Aix-Marseille Universitacute;e) ; Dewolf, B. (Cooperative International Neuromuscular Research Group. Department of Neurology) ; Hutchence, M. (Institute for Neuroscience andMuscle Research. ChildrensHospital atWestmead. University of Sydney) ; Gee, R. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Prügel, J. (ELAN-PHYSIO. Praxis fur Physiotherapie Maron) ; Maron, E. (ELAN-PHYSIO. Praxis fur Physiotherapie Maron) ; Hilsden, H. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Lochmüller, H. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Grieben, U. (ChariteMuscle Research Unit. Experimental and Clinical Research Center. A joint cooperation of the Charitacute;e Medical Faculty) ; Spuler, S. (ChariteMuscle Research Unit. Experimental and Clinical Research Center. A joint cooperation of the Charitacute;e Medical Faculty) ; Rocha, C.T. (Department of Neurology and Neurological Sciences. Stanford University School ofMedicine) ; Day, J.W. (Department of Neurology and Neurological Sciences. Stanford University School ofMedicine) ; Jones, K.J. (Institute for Neuroscience andMuscle Research. ChildrensHospital atWestmead. University of Sydney) ; Bharucha-Goebel, D.X. (NIH) ; Salort-Campana, E. (Centre de Reference des Maladies Neuromusculaires PACA Racute;eunion Rhone Alpes. Hopital de la Timone. Aix-Marseille Universitacute;e) ; Harms, M. (Department of Neurology. Washington University School of Medicine) ; Pestronk, A. (Department of Neurology. Washington University School of Medicine) ; Krause, S. (Friedrich-Baur-Institute. Department of Neurology. Ludwig-Maximilians-University of Munich) ; Schreiber-Katz, O. (Friedrich-Baur-Institute. Department of Neurology. Ludwig-Maximilians-University of Munich) ; Walter, M.C. (Friedrich-Baur-Institute. Department of Neurology. Ludwig-Maximilians-University of Munich) ; Paradas, C. (Neuromuscular Unit. Department of Neurology. Hospital U. Virgen del Rocacute;io/Instituto de Biomedicina de Sevilla) ; Hogrel, J.Y. (Institut deMyologie. AP-HP. GH Pitiacute;e-Salpcirc;etrigrave;ere) ; Stojkovic, T. (Institut deMyologie. AP-HP. GH Pitiacute;e-Salpcirc;etrigrave;ere) ; Takeda, S. (DepartmentofNeurology. NationalCenterHospital. National Center ofNeurology and Psychiatry) ; Mori-Yoshimura, M. (DepartmentofNeurology. NationalCenterHospital. National Center ofNeurology and Psychiatry) ; Bravver, E. (Neuroscience Institute. Carolinas Neuromuscular/ALS-MDA Center. Carolinas HealthCare System) ; Sparks, S. (Neuroscience Institute. Carolinas Neuromuscular/ALS-MDA Center. Carolinas HealthCare System) ; Diaz-Manera, Jordi. (Institut d'Investigació Biomèdica Sant Pau) ; Bello, L. (Institut d'Investigació Biomèdica Sant Pau) ; Semplicini, C. (Institut d'Investigació Biomèdica Sant Pau) ; Pegoraro, E. (Institut d'Investigació Biomèdica Sant Pau) ; Mendell, J.R. (Research Institute at Nationwide Childrens Hospital. TheOhio State University) ; Bushby, K. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Straub, V. (John Walton Muscular Dystrophy Research Centre. Newcastle University and Newcastle Hospitals NHS Foundation Trust. MRC Centre for Neuromuscular Diseases) ; Universitat Autònoma de Barcelona
ObjectiveTo assess the ability of functional measures to detect disease progression in dysferlinopathy over 6 months and 1 year. MethodsOne hundred ninety-three patients with dysferlinopathy were recruited to the Jain Foundation's International Clinical Outcome Study for Dysferlinopathy. [...]
2019 - 10.1212/WNL.0000000000006858
Neurology, Vol. 92 Núm. 5 (29 2019) , p. E461-E474  

See also: similar author names
2 Méndez, J.
1 Méndez, J. M.
2 Méndez, Jorge
1 Méndez, Jose Carlos
1 Méndez, Josep M.
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