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Secondary C1q Deficiency in Activated PI3Kδ Syndrome Type 2.
Hong, Ying; Nanthapisal, Sira; Omoyinmi, Ebun; Olbrich, Peter; Neth, Olaf; Speckmann, Carsten; Lucena, Jose Manuel; Gilmour, Kimberly; Worth, Austen; Klein, Nigel; Eleftheriou, Despina; Brogan, Paul.
Afiliação
  • Hong Y; Infection, Immunology and Inflammation Research & Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Nanthapisal S; Infection, Immunology and Inflammation Research & Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Omoyinmi E; Department of Pediatrics, Thammasat University, Bangkok, Thailand.
  • Olbrich P; Infection, Immunology and Inflammation Research & Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Neth O; Paediatric Infectious Diseases, Rheumatology and Immunology Unit, Institut of Biomedicine of Seville, Hospital Universitario Virgen del Rocío, Seville, Spain.
  • Speckmann C; Paediatric Infectious Diseases, Rheumatology and Immunology Unit, Institut of Biomedicine of Seville, Hospital Universitario Virgen del Rocío, Seville, Spain.
  • Lucena JM; Faculty of Medicine, Center for Chronic Immunodeficiency, Medical Center, University of Freiburg, Freiburg im Breisgau, Germany.
  • Gilmour K; Unidad de Inmunología, Hospital Universitario Virgen del Rocio, Seville, Spain.
  • Worth A; Clinical Immunology Laboratory, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Eleftheriou D; Infection, Immunology and Inflammation Research & Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Brogan P; Infection, Immunology and Inflammation Research & Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
Front Immunol ; 10: 2589, 2019.
Article em En | MEDLINE | ID: mdl-31781101
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complemento C1q / Classe I de Fosfatidilinositol 3-Quinases / Doenças da Imunodeficiência Primária Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Suíça
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complemento C1q / Classe I de Fosfatidilinositol 3-Quinases / Doenças da Imunodeficiência Primária Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Suíça