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Plasma C3d levels as a diagnostic marker for complete complement factor I deficiency.
Naesens, Leslie; Smet, Julie; Tavernier, Simon J; Schelstraete, Petra; Hoste, Levi; Lambrecht, Stijn; Verhelst, Helene; van der Werff Ten Bosch, Jutte; Ferster, Alina; Blumental, Sophie; Hilbert, Pascale; Kerre, Tessa; Vande Walle, Johan; Licht, Christoph; Roumenina, Lubka T; Stordeur, Patrick; Haerynck, Filomeen.
Afiliación
  • Naesens L; Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium; Department of Hematology, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent Universi
  • Smet J; Belgian National Reference Center for the Complement System, Laboratory of Immunology, LHUB-ULB, Université Libre de Bruxelles, Brussels, Belgium.
  • Tavernier SJ; Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium; Laboratory of Immunoregulation, VIB Inflammation Research Center, Ghent, Belgium.
  • Schelstraete P; Department of Pediatrics, Division of Pediatric Pulmonology, Infectious Diseases and Immunology, Ghent University Hospital, Ghent, Belgium.
  • Hoste L; Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Pulmonology, Infectious Diseases and Immunology, Ghent University Hospital, Ghent
  • Lambrecht S; Division of Laboratory Medicine, Department of Clinical Chemistry, Ghent University Hospital, Ghent, Belgium.
  • Verhelst H; Department of Pediatrics, Division of Pediatric Neurology, University Hospital Ghent, Ghent, Belgium.
  • van der Werff Ten Bosch J; Department of Pediatrics, Division of Pediatric Oncology and Immunology, Universitair Ziekenhuis Brussel, Jette, Belgium.
  • Ferster A; Department of Pediatrics, Department of Haematology-Oncology, Children's University Hospital Queen Fabiola, Université Libre de Bruxelles, Brussels, Belgium.
  • Blumental S; Department of Pediatrics, Department of Haematology-Oncology, Children's University Hospital Queen Fabiola, Université Libre de Bruxelles, Brussels, Belgium.
  • Hilbert P; Department of Human Genetics, Institut de Pathologie et Génétique, Gosselies, Belgium.
  • Kerre T; Department of Hematology, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium.
  • Vande Walle J; Department of Pediatrics, Division of Pediatric Nephrology, University Hospital Ghent, Ghent, Belgium.
  • Licht C; Department of Pediatrics, Division of Pediatric Nephrology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Roumenina LT; Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, Paris, France.
  • Stordeur P; Belgian National Reference Center for the Complement System, Laboratory of Immunology, LHUB-ULB, Université Libre de Bruxelles, Brussels, Belgium.
  • Haerynck F; Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Pulmonology, Infectious Diseases and Immunology, Ghent University Hospital, Ghent
J Allergy Clin Immunol ; 147(2): 749-753.e2, 2021 02.
Article en En | MEDLINE | ID: mdl-32853637
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C3 / Biomarcadores / Complemento C3d / Enfermedades por Deficiencia de Complemento Hereditario Tipo de estudio: Diagnostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Allergy Clin Immunol Año: 2021 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C3 / Biomarcadores / Complemento C3d / Enfermedades por Deficiencia de Complemento Hereditario Tipo de estudio: Diagnostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Allergy Clin Immunol Año: 2021 Tipo del documento: Article