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Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study.
Goselink, Rianne J M; Schreuder, Tim H A; van Alfen, Nens; de Groot, Imelda J M; Jansen, Merel; Lemmers, Richard J L F; van der Vliet, Patrick J; van der Stoep, Nienke; Theelen, Thomas; Voermans, Nicol C; van der Maarel, Silvère M; van Engelen, Baziel G M; Erasmus, Corrie E.
Afiliação
  • Goselink RJM; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Schreuder THA; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • van Alfen N; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • de Groot IJM; Department of Rehabilitation, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Jansen M; Department of Rehabilitation, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Lemmers RJLF; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • van der Vliet PJ; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • van der Stoep N; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Theelen T; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Voermans NC; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • van der Maarel SM; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • van Engelen BGM; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Erasmus CE; Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.
Ann Neurol ; 84(5): 627-637, 2018 11.
Article em En | MEDLINE | ID: mdl-30179273
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofia Muscular Facioescapuloumeral Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofia Muscular Facioescapuloumeral Idioma: En Ano de publicação: 2018 Tipo de documento: Article