Inherited factor H dysfunction and complement-associated glomerulonephritis in renal grafts of first and second transplantations

Clinical Transplantation

Volumn 15, Issue , 2001, Pages 45-50

  Watanabe, Seiji ^a   Yamaguchi, Yutaka ^b   Suzuki, Toshiaki ^a   Ikezoe, Masaya ^a   Matsumoto, Naoko ^a   Chikamoto, Hiroko ^a   Nagafuchi, Hiroyuki ^a   Horita, Shigeru ^a   Hattori, Motoshi ^a   Shiraga, Hiroshi ^a   Tokumoto, Tadahiko ^a   Tanabe, Kazunari ^a   Toma, Hiroshi ^a   Ito, Katsumi ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

C3; Electron dense deposit; Factor H; HUS; IgA GN; MPGN

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT FACTOR H; IMMUNOGLOBULIN A;

ADULT; ARTICLE; CASE REPORT; COMPLEMENT DEPOSITION; COMPLEMENT DISORDER; DIALYSIS; DISEASE ASSOCIATION; FATHER; GENETIC DISORDER; HEMOLYTIC UREMIC SYNDROME; HISTOPATHOLOGY; HUMAN; IMMUNOFLUORESCENCE; IMMUNOGLOBULIN A NEPHROPATHY; IMMUNOGLOBULIN DEPOSITION; KIDNEY BIOPSY; KIDNEY DONOR; KIDNEY GRAFT; KIDNEY TRANSPLANTATION; LIVING DONOR; MALE; MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS; MESANGIUM; MICROSCOPY; MOTHER; PATHOGENESIS; PRIORITY JOURNAL; PROTEINURIA; RECURRENT DISEASE; RELATIVE;

ADULT; COMPLEMENT C3; COMPLEMENT FACTOR H; GLOMERULONEPHRITIS, MEMBRANOPROLIFERATIVE; HUMANS; KIDNEY GLOMERULUS; KIDNEY TRANSPLANTATION; MALE;

EID: 0035665689     PISSN: 09020063     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0012.2001.0150s5045.x     Document Type: Article

References (13)

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5. Genetic polymorphism of human factor H (β1H globulin)
6. Incidence of mesangial IgA deposition of renal allograft donors in Japan
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8. Inherited factor H deficiency and collagen glomerulopathy
9. Glomerular deposition and serum levels of complement control proteins in patients with IgA nephropathy
10. Familial hgemolytic-uremic syndrome and homozygous factor H deficiency
11. Human complement factor H deficiency associated with hemolytic uremic syndrome
12. Hypo-complementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Role of factor H abnormalities
13. The role of early renal biopsy in cyclosporine induced thrombotic microangiopathy