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Heterogeneous pattern of renal disease associated with homozygous factor H deficiency
Authors:Servais Aude  Noël Laure-Hélène  Dragon-Durey Marie-Agnes  Gübler Marie-Claire  Rémy Philippe  Buob David  Cordonnier Carole  Makdassi Raïfah  Jaber Waddah  Boulanger Eric  Lesavre Philippe  Frémeaux-Bacchi Véronique
Affiliation:
  • a Department of Nephrology, Hôpital Necker-Enfants Malades AP-HP, Paris 75015, France
  • b Université Paris Descartes, Paris 75006, France
  • c Department of Immunology, Hôpital Européen Georges Pompidou AP-HP, Paris 75015, France
  • d Department of Pathology, Hôpital Necker-Enfants Malades AP-HP, Paris 75015, France
  • e Department of Nephrology, Hôpital Henri Mondor, Créteil 94010, France
  • f Department of Pathology, Hôpital Calmette, Lille 59037, France
  • g Department of Pathology, Hôpital Henri Mondor, Créteil 94010, France
  • h Department of Nephrology, CHU Amiens 80054, France
  • i Department of Nephrology, CH Saint Quentin 02321, France
  • j Department of Nephrology, Hôpital Calmette, Lille 59037, France
  • k INSERM, U 845, Hôpital Necker-Enfants Malades AP-HP, Paris 75015, France
  • l U 574, Hôpital Necker-Enfants Malades AP-HP, Paris 75015, France
  • Abstract:
    Keywords:C3 Nephritic factor   Complement   Alternative pathway   Complement gene mutation   Factor H deficiency   Primary glomerulonephritis
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