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Rhabdomyolysis: a genetic perspective.
Scalco, Renata Siciliani; Gardiner, Alice R; Pitceathly, Robert Ds; Zanoteli, Edmar; Becker, Jefferson; Holton, Janice L; Houlden, Henry; Jungbluth, Heinz; Quinlivan, Ros.
Afiliação
  • Scalco RS; MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London (UCL) Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK. renata_scalco@hotmail.com.
  • Gardiner AR; Department of Neurology, HSL, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Rio Grande do Sul, Brazil. renata_scalco@hotmail.com.
  • Pitceathly RD; CAPES Foundation, Ministry of Education of Brazil, Brasilia, DF, Brazil. renata_scalco@hotmail.com.
  • Zanoteli E; MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London (UCL) Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK. alice.gardiner.10@ucl.ac.uk.
  • Becker J; MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London (UCL) Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK. r.pitceathly@ucl.ac.uk.
  • Holton JL; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London (KCL), London, UK. r.pitceathly@ucl.ac.uk.
  • Houlden H; Department of Neurology, School of Medicine, Universidade de São Paulo (FMUSP), São Paulo, SP, Brazil. zanoteli@terra.com.br.
  • Jungbluth H; Department of Neurology, HSL, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Rio Grande do Sul, Brazil. jeffersonbecker@hotmail.com.
  • Quinlivan R; MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London (UCL) Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK. Janice.holton@ucl.ac.uk.
Orphanet J Rare Dis ; 10: 51, 2015 May 02.
Article em En | MEDLINE | ID: mdl-25929793
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiólise / Predisposição Genética para Doença Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiólise / Predisposição Genética para Doença Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article