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Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.
Fayssoil, A; Laforêt, P; Bougouin, W; Jardel, C; Lombès, A; Bécane, H M; Berber, N; Stojkovic, T; Béhin, A; Eymard, B; Duboc, D; Wahbi, K.
Afiliação
  • Fayssoil A; AP-HP, Pitié-Salpêtrière Hospital, Reference Centre for Muscle Diseases Paris-Est, Myology Institute, Paris, France.
  • Laforêt P; AP-HP, Raymond Poincaré Hospital, Versailles Saint-Quentin en Yvelines University, Garches, France.
  • Bougouin W; AP-HP, Pitié-Salpêtrière Hospital, Reference Centre for Muscle Diseases Paris-Est, Myology Institute, Paris, France.
  • Jardel C; Myology Institute, Pitié-Salpêtrière Hospital, Pierre et Marie Curie Paris 6 University, Paris, France.
  • Lombès A; INSERM Unit 970, Paris Cardiovascular Research Centre (PARCC), Paris, France.
  • Bécane HM; Paris-Descartes, Sorbonne Paris Cité University, Paris, France.
  • Berber N; Medical Intensive Care Unit, AP-HP, Cochin Hospital, Paris, France.
  • Stojkovic T; Biochemistry Department, AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
  • Béhin A; INSERM U1016, CNRS UMR 8104, Institut Cochin, Paris, France.
  • Eymard B; Paris-Descartes, Sorbonne Paris Cité University, Paris, France.
  • Duboc D; INSERM U1016, CNRS UMR 8104, Institut Cochin, Paris, France.
  • Wahbi K; AP-HP, Pitié-Salpêtrière Hospital, Reference Centre for Muscle Diseases Paris-Est, Myology Institute, Paris, France.
Eur J Neurol ; 24(2): 255-261, 2017 02.
Article em En | MEDLINE | ID: mdl-27869334
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: DNA Mitocondrial / Síndrome MELAS / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: DNA Mitocondrial / Síndrome MELAS / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França