Complement dysregulation in haemolytic uraemic syndrome

被引：8

作者：

Bonnardeaux, A ^{[1
]}

Pichette, V ^{[1
]}

机构：

[1] Univ Montreal, Hop Maison Neuve Rosemont, Serv Nephrol, Montreal, PQ H1T 2M4, Canada

来源：

LANCET | 2003年 / 362卷 / 9395期

关键词：

D O I：

10.1016/S0140-6736(03)14777-0

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1514 / 1515

页数：2

共 9 条

[1]

CAPRIOLI J, 2003, HUM MOL GENET 1028

[2] Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor [J].

Donne, RL ;

Abbs, I ;

Barany, P ;

Elinder, CG ;

Little, M ;

Conlon, P ;

Goodship, THJ .

AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 40 (06)

[3] Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome - A systematic review, meta-analysis, and meta-regression [J].

Garg, AX ;

Suri, RS ;

Barrowman, N ;

Rehman, F ;

Matsell, D ;

Rosas-Arellano, MP ;

Salvadori, M ;

Haynes, RB ;

Clark, WF .

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (10) :1360-1370

[4] The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children [J].

Loirat, C ;

Niaudet, P .

PEDIATRIC NEPHROLOGY, 2003, 18 (11) :1095-1101

[5] FAMILIAL HEMOLYTIC-UREMIC SYNDROME AND HOMOZYGOUS FACTOR-H DEFICIENCY [J].

PICHETTE, V ;

QUERIN, S ;

SCHURCH, W ;

BRUN, G ;

LEHNERNETSCH, G ;

DELAGE, JM .

AMERICAN JOURNAL OF KIDNEY DISEASES, 1994, 24 (06) :936-941

[6] Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome [J].

Richards, A ;

Kemp, EJ ;

Liszewski, MK ;

Goodship, JA ;

Lampe, AK ;

Decorte, R ;

Müslümanoglu, MH ;

Kavukcu, S ;

Filler, G ;

Pirson, Y ;

Wen, LS ;

Atkinson, JP ;

Goodship, THJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12966-12971

[7] Post-transplant hemolytic-uremic syndrome [J].

Ruggenenti, P ;

Noris, M ;

Cohen, JJ ;

Schieppati, A ;

Remuzzi, G ;

Perico, N ;

Zoja, C ;

Gregorini, G ;

Galbusera, M .

KIDNEY INTERNATIONAL, 2002, 62 (03) :1093-1104

[8] Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura [J].

Ruggenenti, P ;

Noris, M ;

Remuzzi, G .

KIDNEY INTERNATIONAL, 2001, 60 (03) :831-846

[9] Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome [J].

Veyradier, A ;

Obert, B ;

Haddad, E ;

Cloarec, S ;

Nivet, H ;

Foulard, M ;

Lesure, F ;

Delattre, P ;

Lakhdari, M ;

Meyer, D ;

Girma, JP ;

Loriat, C .

JOURNAL OF PEDIATRICS, 2003, 142 (03) :310-317

← 1 →