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Mimicking Behçet's disease: GM-CSF gain of function mutation in a family suffering from a Behçet's disease-like disorder marked by extreme pathergy.
Rösler, B; Heinhuis, B; Wang, X; Silvestre, R; Joosten, L A B; Netea, M G; Arts, P; Mantere, T; Lefeber, D J; Hoischen, A; van de Veerdonk, F L.
Afiliação
  • Rösler B; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
  • Heinhuis B; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
  • Wang X; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
  • Silvestre R; Microbiology and Infection Research Domain, Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.
  • Joosten LAB; ICVS/3B's, PT Government Associate Laboratory, Guimarães, Portugal.
  • Netea MG; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
  • Arts P; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
  • Mantere T; Department for Genomics and Immunoregulation, Life and Medical Sciences Institute (LIMES), University of Bonn, Bonn, Germany.
  • Lefeber DJ; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Hoischen A; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • van de Veerdonk FL; Department of Neurology, Translational Metabolic Laboratory, Radboud University Medical Centre, Nijmegen, the Netherlands.
Clin Exp Immunol ; 204(2): 189-198, 2021 05.
Article em En | MEDLINE | ID: mdl-33349924
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Behçet / Fator Estimulador de Colônias de Granulócitos e Macrófagos / Mutação com Ganho de Função Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Clin Exp Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Behçet / Fator Estimulador de Colônias de Granulócitos e Macrófagos / Mutação com Ganho de Função Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Clin Exp Immunol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda