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Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I.
Nanthapisal, Sira; Eleftheriou, Despina; Gilmour, Kimberly; Leone, Valentina; Ramnath, Radhika; Omoyinmi, Ebun; Hong, Ying; Klein, Nigel; Brogan, Paul A.
Afiliação
  • Nanthapisal S; Infection Inflammation and Rheumatology Section, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Eleftheriou D; Department of Pediatrics, Faculty of Medicine, Thammasat University, Pathumthani, Thailand.
  • Gilmour K; Infection Inflammation and Rheumatology Section, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Leone V; Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Ramnath R; Department of Paediatric Rheumatology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
  • Omoyinmi E; Department of Histopathology, St. James University Hospital, Leeds, United Kingdom.
  • Hong Y; Infection Inflammation and Rheumatology Section, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Klein N; Infection Inflammation and Rheumatology Section, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
  • Brogan PA; Infection Inflammation and Rheumatology Section, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom.
Front Immunol ; 9: 735, 2018.
Article em En | MEDLINE | ID: mdl-29696024
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complemento C3 / Fator I do Complemento / Vasculite Leucocitoclástica Cutânea / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2018 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 C3 / Fator I do Complemento / Vasculite Leucocitoclástica Cutânea / Doenças Genéticas Inatas Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Suíça