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Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.
Ardicli, Didem; Taskiran, Ekim Z; Kosukcu, Can; Temucin, Cagri; Oguz, Kader K; Haliloglu, Goknur; Alikasifoglu, Mehmet; Topaloglu, Haluk.
  • Ardicli D; Department of Pediatric Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Taskiran EZ; Department of Medical Genetics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Kosukcu C; Department of Medical Genetics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Temucin C; Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Oguz KK; Department of Radiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Haliloglu G; Department of Pediatric Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Alikasifoglu M; Department of Medical Genetics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
  • Topaloglu H; Department of Pediatric Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Neuropediatrics ; 48(6): 477-481, 2017 12.
Article en En | MEDLINE | ID: mdl-28800659
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antígenos CD59 / Síndrome de Guillain-Barré / Hemoglobinuria / Anemia Hemolítica Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antígenos CD59 / Síndrome de Guillain-Barré / Hemoglobinuria / Anemia Hemolítica Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Año: 2017 Tipo del documento: Article