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Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene.
Denier, Christian; Balu, Laurent; Husson, Béatrice; Nasser, Ghaidaa; Burglen, Lydie; Rodriguez, Diana; Labauge, Pierre; Chevret, Laurent.
Afiliação
  • Denier C; Department of Neurology, Bicêtre Hospital, Assistance-Publique-Hôpitaux de Paris (AP-HP), France. Electronic address: christian.denier@bct.aphp.fr.
  • Balu L; Department of Pediatry, Bicêtre Hospital, Assistance-Publique-Hôpitaux de Paris (AP-HP), France.
  • Husson B; Department of Radiology, Bicêtre Hospital, Assistance-Publique-Hôpitaux de Paris (AP-HP), France.
  • Nasser G; Department of Radiology, Bicêtre Hospital, Assistance-Publique-Hôpitaux de Paris (AP-HP), France.
  • Burglen L; Department of Genetics, Trousseau Hospital, AP-HP, France.
  • Rodriguez D; Department of Pediatry, Robert Debré Hospital, AP-HP, France.
  • Labauge P; Department of Neurology, Montpellier Hospital, France.
  • Chevret L; Department of Neurology, Bicêtre Hospital, Assistance-Publique-Hôpitaux de Paris (AP-HP), France.
J Neurol Sci ; 345(1-2): 236-8, 2014 Oct 15.
Article em En | MEDLINE | ID: mdl-25128471
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saúde da Família / Chaperonas Moleculares / Leucoencefalite Hemorrágica Aguda / Complexo de Proteínas Formadoras de Poros Nucleares / Mutação Limite: Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saúde da Família / Chaperonas Moleculares / Leucoencefalite Hemorrágica Aguda / Complexo de Proteínas Formadoras de Poros Nucleares / Mutação Limite: Child, preschool / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article