Membranous nephropathy in a patient with hereditary complete complement C4 deficiency

被引：12
|
作者：
Lhotta, K
Würzner, R
Rumpelt, HJ
Eder, P
Mayer, G
机构：
[1] Univ Innsbruck Hosp, Dept Internal Med, Div Clin Nephrol, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Inst Hyg & Social Med, A-6020 Innsbruck, Austria
[3] SLK Klinikum, Inst Pathol, Heilbronn, Germany
来源：
NEPHROLOGY DIALYSIS TRANSPLANTATION | 2004年 / 19卷 / 04期
关键词：
complement C4; i.v; immunoglobulin; membranous nephropathy; mycophenolate mofetil;
D O I：
10.1093/ndt/gfh008
中图分类号：
R3 [基础医学]; R4 [临床医学];
学科分类号：
1001 ; 1002 ; 100602 ;
摘要：
[No abstract available]
引用
收藏
页码：990 / 993
页数：4
相关论文
共 50 条
  • [1] A patient with complete C4 deficiency and membranous nephropathy:: response to intravenous immunoglobulin
    Lhotta, K
    Eder, P
    Rumpelt, HJ
    Mayer, G
    Würzner, R
    MOLECULAR IMMUNOLOGY, 2001, 38 (2-3) : 107 - 107
  • [2] Renal AA Amyloidosis in a Patient with Hereditary Complete Complement C4 Deficiency
    Helal, Imed
    Goucha, Rym
    Ben Hamida, Fethi
    Elyounsi, Fethi
    Ben Maiz, Hedi
    Kheder, Adel
    SAUDI JOURNAL OF KIDNEY DISEASES AND TRANSPLANTATION, 2011, 22 (05) : 1008 - 1011
  • [3] Kidney transplantation in patients suffering from hereditary complete complement C4 deficiency
    Falkeis, Christina
    Mark, Walter
    Sergi, Consolato
    Heininger, Dorothea
    Neumair, Friedrich
    Scheiring, Johanna
    Lhotta, Karl
    TRANSPLANT INTERNATIONAL, 2007, 20 (12) : 1044 - 1049
  • [4] Recurrent hematuria: A novel clinical presentation of hereditary complete complement C4 deficiency
    Lhotta, K
    Neunhauserer, M
    Solder, B
    UringLambert, B
    Wurzner, R
    Rumpelt, HJ
    Konig, P
    AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (03) : 424 - 427
  • [5] Clinico-pathological experience with kidney transplantation in hereditary complete complement c4 deficiency
    Falkeis, C.
    Grissmann, T.
    Mark, W.
    Neumair, F.
    Mikuz, G.
    Lhotta, K.
    Sergi, C.
    PATHOLOGY RESEARCH AND PRACTICE, 2007, 203 (05) : 314 - 315
  • [6] ANALYSIS OF COMPLEMENT C4 LOCI IN CAUCASOIDS AND JAPANESE WITH IDIOPATHIC MEMBRANOUS NEPHROPATHY
    SACKS, SH
    NOMURA, S
    WARNER, C
    NAITO, S
    OGAHARA, S
    VAUGHAN, R
    BRIGGS, D
    KIDNEY INTERNATIONAL, 1992, 42 (04) : 882 - 887
  • [7] Cerebral vasculitis in a patient with hereditary complete C4 deficiency and systemic lupus erythematosus
    Lhotta, K
    Würzner, R
    Rosenkranz, AR
    Beer, R
    Rudisch, A
    Neumair, F
    Mayer, G
    LUPUS, 2004, 13 (02) : 139 - 141
  • [8] Cerebral vaculitis in a patient with hereditary complete C4 deficiency and systemic lupus erythematosus
    Lhotta, K
    Würzner, R
    Rosenkranz, AR
    Vogl, G
    Beer, R
    Rudisch, A
    Neumair, F
    Mayer, G
    MOLECULAR IMMUNOLOGY, 2003, 40 (2-4) : 224 - 224
  • [9] A novel mutation of the fourth complement component (C4) resulting a complete C4 deficiency in a moroccan systemic lupus erythernatosus (SLE) patient
    Wu, Yee Ling
    Hauptmann, Georges
    Zhou, Bi
    Yu, C. Yung
    MOLECULAR IMMUNOLOGY, 2007, 44 (1-3) : 259 - 259
  • [10] Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency
    Florian Knoll
    Emanuel Zitt
    Denis Intemann
    Karl Lhotta
    BMC Nephrology, 13
12345