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
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
收藏
页码:1676 / 1687
页数:12
相关论文
共 102 条
[51]   Familial hemolytic uremic syndrome associated with complement factor H deficiency [J].
Landau, D ;
Shalev, H ;
Levy-Finer, G ;
Polonsky, A ;
Segev, Y ;
Katchko, L .
JOURNAL OF PEDIATRICS, 2001, 138 (03) :412-417
[52]   Efficacy of plasma therapy in atypical hemolytic uremic syndrome with complement factor H mutations [J].
Lapeyraque, Anne-Laure ;
Wagner, Eric ;
Phan, Veronique ;
Clermont, Marie-Jose ;
Merouani, Aicha ;
Fremeaux-Bacchi, Veronique ;
Goodship, Timothy H. J. ;
Robitaille, Pierre .
PEDIATRIC NEPHROLOGY, 2008, 23 (08) :1363-1366
[53]   Complement mutation-associated de novo thrombotic microangiopathy following kidney transplantation [J].
Le Quintrec, M. ;
Lionet, A. ;
Kamar, N. ;
Karras, A. ;
Barbier, S. ;
Buchler, M. ;
Fakhouri, F. ;
Provost, F. ;
Fridiman, W. H. ;
Thervet, E. ;
Legendre, C. ;
Zuber, J. ;
Fremeaux-Bacchi, V. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2008, 8 (08) :1694-1701
[54]   Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15 [J].
Licht, C ;
Weyersberg, A ;
Heinen, S ;
Stapenhorst, L ;
Devenge, J ;
Beck, B ;
Waldherr, R ;
Kirschfink, M ;
Zipfel, PF ;
Hoppe, B .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2005, 45 (02) :415-421
[55]   Dissecting sites important for complement regulatory activity in membrane cofactor protein (MCP; CD46) [J].
Liszewski, MK ;
Leung, M ;
Cui, WY ;
Subramanian, VB ;
Parkinson, J ;
Barlow, PN ;
Manchester, M ;
Atkinson, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37692-37701
[56]   TREATMENT OF THE CHILDHOOD HEMOLYTIC UREMIC SYNDROME WITH PLASMA - A MULTICENTER RANDOMIZED CONTROLLED TRIAL [J].
LOIRAT, C ;
SONSINO, E ;
HINGLAIS, N ;
JAIS, JP ;
LANDAIS, P ;
FERMANIAN, J .
PEDIATRIC NEPHROLOGY, 1988, 2 (03) :279-285
[57]   Complement and the atypical hemolytic uremic syndrome in children [J].
Loirat, Chantal ;
Noris, Marina ;
Fremeaux-Bacchi, Veronique .
PEDIATRIC NEPHROLOGY, 2008, 23 (11) :1957-1972
[58]   Hemolytic uremic syndrome recurrence after renal transplantation [J].
Loirat, Chantal ;
Fremeaux-Bacchi, Veronique .
PEDIATRIC TRANSPLANTATION, 2008, 12 (06) :619-629
[59]   Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome [J].
Manuelian, T ;
Hellwage, J ;
Meri, S ;
Caprioli, J ;
Noris, M ;
Heinen, S ;
Jozsi, M ;
Neumann, HPH ;
Remuzzi, G ;
Zipfel, PF .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (08) :1181-1190
[60]   The complement factor h R1210C mutation is associated with atypical hemolytic uremic syndrome [J].
Martinez-Barricarte, Ruben ;
Pianetti, Gaia ;
Gautard, Ruxandra ;
Misselwitz, Joachim ;
Strain, Lisa ;
Fremeaux-Bacchi, Veronique ;
Skerka, Christine ;
Zipfel, Peter F. ;
Goodship, Tim ;
Noris, Marina ;
Remuzzi, Giuseppe ;
De Cordoba, Santiago Rodriguez .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 19 (03) :639-646