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Artículos, Encontrados 2 registros
Artículos Encontrados 2 registros  
1.
14 p, 8.0 MB Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy / Reyngoudt, Harmen (NMR Laboratory) ; Smith, Fiona Elizabeth (Newcastle University) ; Caldas de A. Araújo, Ericky (NMR Laboratory) ; Wilson, Ian (Newcastle University) ; Fernandez-Torron, Roberto (Hospital de Donostia (Sant Sebastià, País Basc)) ; James, Meredith K. (Newcastle University) ; Moore, Ursula (Newcastle University) ; Diaz-Manera, Jordi (Institut d'Investigació Biomèdica Sant Pau) ; Marty, Benjamin (NMR Laboratory) ; Azzabou, Noura (NMR Laboratory) ; Gordish-Dressman, Heather (George Washington University) ; Rufibach, Laura E. (The JAIN Foundation) ; Hodgson, Tim (Newcastle University) ; Wallace, Dorothy (Newcastle University) ; Ward, Louise (Newcastle University) ; Boisserie, Jean Marc (NMR Laboratory) ; Le Louër, Julien (NMR Laboratory) ; Hilsden, Heather (Newcastle University) ; Sutherland, Helen (Newcastle University) ; Canal, Aurélie (Institute of Myology) ; Hogrel, J.Y (Institut de Myologie (París, França)) ; Jacobs, Marni (George Washington University) ; Stojkovic, Tanya (Institut deMyologie (París, França)) ; Bushby, Kate (Newcastle University) ; Mayhew, Anna G. (Newcastle University) ; Straub, Volker (Newcastle University) ; Carlier, Pierre G. (University Paris-Saclay) ; Blamire, Andrew (Newcastle University) ; Universitat Autònoma de Barcelona
Natural history studies in neuromuscular disorders are vital to understand the disease evolution and to find sensitive outcome measures. We performed a longitudinal assessment of quantitative magnetic resonance imaging (MRI) and phosphorus magnetic resonance spectroscopy (P MRS) outcome measures and evaluated their relationship with function in lower limb skeletal muscle of dysferlinopathy patients. [...]
2022 - 10.1002/jcsm.12987
Journal of Cachexia, Sarcopenia and Muscle, Vol. 13 Núm. 3 (june 2022) , p. 1850-1863  
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2.
10 p, 585.1 KB Water T2 could predict functional decline in patients with dysferlinopathy / Moore, Ursula. (The John Walton Muscular Dystrophy Research Centre. Translational and Clinical Research Institute. Newcastle University and Newcastle Hospitals NHS Foundation Trust) ; Caldas de A. Araújo, Ericky (NMR Laboratory. CEA/DRF/IBFJ/MIRCen) ; Reyngoudt, Harmen (NMR Laboratory. CEA/DRF/IBFJ/MIRCen) ; Gordish-Dressman, Heather (Pediatrics. Epidemiology and Biostatistics. George Washington University) ; Smith, Fiona E. (Magnetic Resonance Centre. Translational and Clinical Research Institute. Newcastle University) ; Wilson, Ian (Magnetic Resonance Centre. Translational and Clinical Research Institute. Newcastle University) ; James, Meredith (The John Walton Muscular Dystrophy Research Centre. Translational and Clinical Research Institute. Newcastle University and Newcastle Hospitals NHS Foundation Trust) ; Mayhew, Anna (The John Walton Muscular Dystrophy Research Centre. Translational and Clinical Research Institute. Newcastle University and Newcastle Hospitals NHS Foundation Trust) ; Rufibach, Laura (Jain Foundation) ; Day, John W. (Department of Neurology and Neurological Sciences. Stanford University School of Medicine) ; Jones, Kristi J. (The Children's Hospital at Westmead and The University of Sydney) ; Bharucha-Goebel, Diana (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ; Salort-Campana, Emmanuelle (Service des maladies neuromusculaire et de la SLA. Hôpital de La Timone) ; Pestronk, Alan (Washington University School of Medicine) ; Walter, Maggie C. (Friedrich-Baur-Institute. Department of Neurology. Ludwig-Maximilians-University of Munich) ; Paradas, Carmen (Instituto de Biomedicina de Sevilla) ; Stojkovic, Tanya (Centre de référence des maladies neuromusculaires. Institut de Myologie. AP-HP. Sorbonne Université. Hôpital Pitié-Salpêtrière) ; Mori-Yoshimura, Madoka (Department of Neurology. National Center Hospital. National Center of Neurology and Psychiatry) ; Bravver, Elena (Neuroscience Institute. Carolinas Neuromuscular/ALS-MDA Center. Carolinas HealthCare System) ; Pegoraro, Elena (Department of Neuroscience. University of Padova) ; Mendell, Jerry R. (The Abigail Wexner Research Institute at Nationwide Children's Hospital) ; Bushby, Kate (The John Walton Muscular Dystrophy Research Centre. Translational and Clinical Research Institute. Newcastle University and Newcastle Hospitals NHS Foundation Trust) ; Blamire, Andrew (Magnetic Resonance Centre. Translational and Clinical Research Institute. Newcastle University) ; Straub, Volker (Newcastle University) ; Carlier, Pierre G. (Université Paris-Saclay. CEA. DRF. Service Hospitalier Frederic Joliot) ; Diaz-Manera, Jordi (Institut d'Investigació Biomèdica Sant Pau)
Background: Water T2 (T2) mapping is increasingly being used in muscular dystrophies to assess active muscle damage. It has been suggested as a surrogate outcome measure for clinical trials. Here, we investigated the prognostic utility of T2 to identify changes in muscle function over time in limb girdle muscular dystrophies. [...]
2022 - 10.1002/jcsm.13063
Journal of Cachexia, Sarcopenia and Muscle, Vol. 13 Núm. 6 (december 2022) , p. 2888-2897  
Registro completo - Creative Commons

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