Your browser doesn't support javascript.
loading
Tracking disease progression non-invasively in Duchenne and Becker muscular dystrophies.
Spitali, Pietro; Hettne, Kristina; Tsonaka, Roula; Charrout, Mohammed; van den Bergen, Janneke; Koeks, Zaïda; Kan, Hermien E; Hooijmans, Melissa T; Roos, Andreas; Straub, Volker; Muntoni, Francesco; Al-Khalili-Szigyarto, Cristina; Koel-Simmelink, Marleen J A; Teunissen, Charlotte E; Lochmüller, Hanns; Niks, Erik H; Aartsma-Rus, Annemieke.
Afiliación
  • Spitali P; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Hettne K; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Tsonaka R; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Charrout M; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • van den Bergen J; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Koeks Z; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Kan HE; C.J. Gorter Center for High Field MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • Hooijmans MT; C.J. Gorter Center for High Field MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
  • Roos A; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK.
  • Straub V; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK.
  • Muntoni F; Dubowitz Neuromuscular Centre, University College London Great Ormond Street Institute of Child Health, London, UK.
  • Al-Khalili-Szigyarto C; Division of Proteomics, School of Biotechnology, KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Koel-Simmelink MJA; Neurochemistry Lab and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center Amsterdam, The Netherlands.
  • Teunissen CE; Neurochemistry Lab and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center Amsterdam, The Netherlands.
  • Lochmüller H; John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, University of Newcastle, Newcastle upon Tyne, UK.
  • Niks EH; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Aartsma-Rus A; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
J Cachexia Sarcopenia Muscle ; 9(4): 715-726, 2018 08.
Article en En | MEDLINE | ID: mdl-29682908
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Middle aged Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Middle aged Idioma: En Revista: J Cachexia Sarcopenia Muscle Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos