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A rare case: childhood-onset C3 glomerulonephritis due to homozygous factor H deficiency.
Rusai, Krisztina; Zaller, Vera; Szilagyi, Agnes; Kain, Renate; Prohaszka, Zoltan; Cook, H Terence; Aufricht, Christoph; Arbeiter, Klaus.
Afiliação
  • Rusai K; Department of Pediatrics and Adolescent Medicine, Pediatric Nephrology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria. krisztina.rusai@meduniwien.ac.at.
  • Zaller V; Department of Pediatrics and Adolescent Medicine, Pediatric Nephrology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
  • Szilagyi A; 3rd Department of Internal Medicine, Research Laboratory, Semmelweis University, Kútvölgyi út 4, Budapest, 1125, Hungary.
  • Kain R; Department of Pathology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
  • Prohaszka Z; 3rd Department of Internal Medicine, Research Laboratory, Semmelweis University, Kútvölgyi út 4, Budapest, 1125, Hungary.
  • Cook HT; Centre for Complement and Inflammation Research, Imperial College, South Kensington Campus, London, SW7 2AZ, UK.
  • Aufricht C; Department of Pediatrics and Adolescent Medicine, Pediatric Nephrology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
  • Arbeiter K; Department of Pediatrics and Adolescent Medicine, Pediatric Nephrology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
CEN Case Rep ; 2(2): 234-238, 2013 Nov.
Article em En | MEDLINE | ID: mdl-28509298

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: CEN Case Rep Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: CEN Case Rep Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Áustria