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Water T2 could predict functional decline in patients with dysferlinopathy.
Moore, Ursula; Caldas de Almeida Araújo, Ericky; Reyngoudt, Harmen; Gordish-Dressman, Heather; Smith, Fiona E; Wilson, Ian; James, Meredith; Mayhew, Anna; Rufibach, Laura; Day, John W; Jones, Kristi J; Bharucha-Goebel, Diana X; Salort-Campana, Emmanuelle; Pestronk, Alan; Walter, Maggie C; Paradas, Carmen; Stojkovic, Tanya; Mori-Yoshimura, Madoka; Bravver, Elena; Pegoraro, Elena; Mendell, Jerry R; Bushby, Kate; Blamire, Andrew M; Straub, Volker; Carlier, Pierre G; Diaz-Manera, Jordi.
Afiliación
  • Moore U; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Caldas de Almeida Araújo E; NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
  • Reyngoudt H; NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.
  • Gordish-Dressman H; NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
  • Smith FE; NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.
  • Wilson I; Center for Translational Science, Division of Biostatistics and Study Methodology, Children's National Health System, Washington, DC, USA.
  • James M; Pediatrics, Epidemiology and Biostatistics, George Washington University, Washington, DC, USA.
  • Mayhew A; Magnetic Resonance Centre, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Rufibach L; Magnetic Resonance Centre, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Day JW; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Jones KJ; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
  • Bharucha-Goebel DX; Jain Foundation, Seattle, WA, USA.
  • Salort-Campana E; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.
  • Pestronk A; The Children's Hospital at Westmead and The University of Sydney, Sydney, NSW, Australia.
  • Walter MC; Department of Neurology, Children's National Health System, Washington, DC, USA.
  • Paradas C; National Institutes of Health (NINDS), Bethesda, MD, USA.
  • Stojkovic T; Service des maladies neuromusculaire et de la SLA, Hôpital de La Timone, Marseille, France.
  • Mori-Yoshimura M; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
  • Bravver E; Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Munich, Germany.
  • Pegoraro E; Neuromuscular Unit, Department of Neurology, Hospital U. Virgen del Rocío/Instituto de Biomedicina de Sevilla, Sevilla, Spain.
  • Mendell JR; Centre de référence des maladies neuromusculaires, Institut de Myologie, AP-HP, Sorbonne Université, Hôpital Pitié-Salpêtrière, Paris, France.
  • Bushby K; Neuroscience Institute, Carolinas Neuromuscular/ALS-MDA Center, Carolinas HealthCare System, Charlotte, NC, USA.
  • Blamire AM; Department of Neuroscience, University of Padova, Padua, Italy.
  • Straub V; The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
  • Diaz-Manera J; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
J Cachexia Sarcopenia Muscle ; 13(6): 2888-2897, 2022 12.
Article en En | MEDLINE | ID: mdl-36058852
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Cinturas / Distrofias Musculares Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Cinturas / Distrofias Musculares Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Alemania