Factor H deficiency and fibrillary glomerulopathy

被引：13

作者：

Bircan, Z ^{[1
]}

Toprak, D

Kilicaslan, I

Solakoglu, S

Uysal, V

Ponard, D

Turker, G

机构：

[1] Kocaeli Univ, Tip Fak Hastanesi, Sch Med, Div Pediat Nephrol, Derince, Turkey

[2] Turkey Istanbul Univ, Sch Med, Dept Pathol, Istanbul, Turkey

[3] CHU Grenoble, Immunol Lab, F-38043 Grenoble, France

来源：

NEPHROLOGY DIALYSIS TRANSPLANTATION | 2004年 / 19卷 / 03期

关键词：

cyclosporine A; factor H; fibrillary glomerulopathy; nephrotic proteinuria;

D O I：

10.1093/ndt/gfg605

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

页码：727 / 730

页数：4

共 11 条

[1] Factor H and the pathogenesis of renal diseases [J].

Ault, BH .

PEDIATRIC NEPHROLOGY, 2000, 14 (10-11) :1045-1053

[2] Long-term effects of cyclosporine A in Alport's syndrome [J].

Callís, L ;

Vila, A ;

Carrera, M ;

Nieto, J .

KIDNEY INTERNATIONAL, 1999, 55 (03) :1051-1056

[3]

Caprioli J, 2001, J AM SOC NEPHROL, V12, P297, DOI 10.1681/ASN.V122297

[4] Cyclosporine A slows the progressive renal disease of Alport syndrome (X-linked hereditary nephritis): Results from a canine model [J].

Chen, D ;

Jefferson, B ;

Harvey, SJ ;

Zheng, KQ ;

Gartley, CJ ;

Jacobs, RM ;

Thorner, PS .

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (03) :690-698

[5] H DEFICIENCY IN 2 BROTHERS WITH ATYPICAL DENSE INTRAMEMBRANOUS DEPOSIT DISEASE [J].

LEVY, M ;

HALBWACHSMECARELLI, L ;

GUBLER, MC ;

KOHOUT, G ;

BENSENOUCI, A ;

NIAUDET, P ;

HAUPTMANN, G ;

LESAVRE, P .

KIDNEY INTERNATIONAL, 1986, 30 (06) :949-956

[6] A FAMILIAL DEFICIENCY OF COMPLEMENT FACTOR-H [J].

LOPEZLARREA, C ;

DIEGUEZ, MA ;

ENGUIX, A ;

DOMINGUEZ, O ;

MARIN, B ;

GOMEZ, E .

BIOCHEMICAL SOCIETY TRANSACTIONS, 1987, 15 (04) :648-649

[7] Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H - Original article [J].

Ohali, M ;

Shalev, H ;

Schlesinger, M ;

Katz, Y ;

Kachko, L ;

Carmi, R ;

Sofer, S ;

Landau, D .

PEDIATRIC NEPHROLOGY, 1998, 12 (08) :619-624

[8] Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H [J].

Pickering, MC ;

Cook, HT ;

Warren, J ;

Bygrave, AE ;

Moss, J ;

Walport, MJ ;

Botto, M .

NATURE GENETICS, 2002, 31 (04) :424-428

[9] INHERITED FACTOR-H DEFICIENCY AND COLLAGEN TYPE-III GLOMERULOPATHY [J].

VOGT, BA ;

WYATT, RJ ;

BURKE, BA ;

SIMONTON, SC ;

KASHTAN, CE .

PEDIATRIC NEPHROLOGY, 1995, 9 (01) :11-15

[10] Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency [J].

Warwicker, P ;

Donne, RL ;

Goodship, JA ;

Goodship, THJ ;

Howie, AJ ;

Kumararatne, DS ;

Thompson, RA ;

Taylor, CM .

NEPHROLOGY DIALYSIS TRANSPLANTATION, 1999, 14 (05) :1229-1233

← 1 2 →