MEDICAL PROGRESS Atypical Hemolytic-Uremic Syndrome

被引：915

作者：

Noris, Marina ^{[1
]}

Remuzzi, Giuseppe ^{[1
,2
]}

机构：

[1] Mario Negri Inst Pharmacol Res, Clin Res Ctr Rare Dis Aldo & Cele Dacco, I-24125 Bergamo, Italy

[2] Osped Riuniti Bergamo, Div Nephrol & Dialysis, I-24100 Bergamo, Italy

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2009年 / 361卷 / 17期

关键词：

COMPLEMENT-FACTOR-H; MEMBRANE COFACTOR PROTEIN; THROMBOTIC THROMBOCYTOPENIC PURPURA; LIVER-KIDNEY TRANSPLANTATION; SUCCESSFUL PLASMA THERAPY; FACTOR-I; RENAL-TRANSPLANTATION; REGULATORY PROTEINS; ENDOTHELIAL-CELLS; SELF-ASSOCIATION;

D O I：

10.1056/NEJMra0902814

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1676 / 1687

页数：12

共 102 条

[21]

Devaux P, 1999, EUR J IMMUNOL, V29, P815

[22] 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)

[23] The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome [J].

Dragon-Durey, M-A ;

Blanc, C. ;

Marliot, F. ;

Loirat, C. ;

Blouin, J. ;

Sautes-Fridman, C. ;

Fridman, W. H. ;

Fremeaux-Bacchi, V. .

JOURNAL OF MEDICAL GENETICS, 2009, 46 (07) :447-450

[24] Atypical haemolytic uraemic syndrome and mutations in complement regulator genes [J].

Dragon-Durey, MA ;

Frémeaux-Bacchi, V .

SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 2005, 27 (03) :359-374

[25] Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome [J].

Dragon-Durey, MA ;

Loirat, C ;

Cloarec, S ;

Macher, MA ;

Blouin, J ;

Nivet, H ;

Weiss, L ;

Fridman, WH ;

Frémeaux-Bacchi, V .

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (02) :555-563

[26] Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis:: Report and genetic analysis of 16 cases [J].

Dragon-Durey, MA ;

Frémeaux-Bacchi, V ;

Loirat, C ;

Blouin, J ;

Niaudet, P ;

Deschenes, G ;

Coppo, P ;

Fridman, WH ;

Weiss, L .

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (03) :787-795

[27] Insights into hemolytic uremic syndrome:: Segregation of three independent predisposition factors in a large, multiple affected pedigree [J].

Esparza-Gordillo, J ;

de Jorge, EG ;

Garrido, CA ;

Carreras, L ;

López-Trascasa, M ;

Sánchez-Corral, P ;

de Córdoba, SR .

MOLECULAR IMMUNOLOGY, 2006, 43 (11) :1769-1775

[28] Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome [J].

Fakhouri, Fadi ;

Jablonski, Mathieu ;

Lepercq, Jacques ;

Blouin, Jacques ;

Benachi, Alexandra ;

Hourmant, Maryvonne ;

Pirson, Yves ;

Durrbach, Antoine ;

Grunfeld, Jean-Pierre ;

Knebelmann, Bertrand ;

Fremeaux-Bacchi, Veronique .

BLOOD, 2008, 112 (12) :4542-4545

[29] Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome [J].

Fang, Celia J. ;

Fremeaux-Bacchi, Veronique ;

Liszewski, M. Kathryn ;

Pianetti, Gaia ;

Noris, Marina ;

Goodship, Timothy H. J. ;

Atkinsoni, John P. .

BLOOD, 2008, 111 (02) :624-632

[30] Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome [J].

Fremeaux-Bacchi, V ;

Dragon-Durey, MA ;

Blouin, J ;

Vigneau, C ;

Kuypers, D ;

Boudailliez, B ;

Loirat, C ;

Rondeau, E ;

Fridman, WH .

JOURNAL OF MEDICAL GENETICS, 2004, 41 (06) :e84

← 1 2 3 4 5 6 7 8 9 10 →