-
1
-
-
70350279315
-
Atypical hemolytic-uremic syndrome
-
Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med 2009 361 (17) 1676-1687
-
(2009)
N Engl J Med
, vol.361
, Issue.17
, pp. 1676-1687
-
-
Noris, M.1
Remuzzi, G.2
-
2
-
-
33747159590
-
Genetics of HUS: The impact of MCP, CFH, and if mutations on clinical presentation, response to treatment, and outcome
-
International Registry of Recurrent and Familial HUS/TTP
-
Caprioli J, Noris M, Brioschi S et al, International Registry of Recurrent and Familial HUS/TTP. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 2006 108 (4) 1267-1279
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
-
3
-
-
34547633064
-
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
-
French Society of Pediatric Nephrology
-
Sellier-Leclerc A L., Freméaux-Bacchi V, Dragon-Durey M A. et al, French Society of Pediatric Nephrology. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol 2007 18 (8) 2392-2400
-
(2007)
J Am Soc Nephrol
, vol.18
, Issue.8
, pp. 2392-2400
-
-
Sellier-Leclerc, A.L.1
Freméaux-Bacchi, V.2
Dragon-Durey, M.A.3
-
4
-
-
53749084348
-
Complement and the atypical hemolytic uremic syndrome in children
-
Loirat C, Noris M, Frémeaux-Bacchi V. Complement and the atypical hemolytic uremic syndrome in children. Pediatr Nephrol 2008 23 (11) 1957-1972
-
(2008)
Pediatr Nephrol
, vol.23
, Issue.11
, pp. 1957-1972
-
-
Loirat, C.1
Noris, M.2
Frémeaux-Bacchi, V.3
-
5
-
-
0017588199
-
Treatment of thrombotic thrombocytopenic purpura with plasma
-
Byrnes J J., Khurana M. Treatment of thrombotic thrombocytopenic purpura with plasma. N Engl J Med 1977 297 (25) 1386-1389
-
(1977)
N Engl J Med
, vol.297
, Issue.25
, pp. 1386-1389
-
-
Byrnes, J.J.1
Khurana, M.2
-
6
-
-
0017727056
-
Plasmapheresis in the treatment of thrombotic thrombocytopenic purpura
-
Bukowski R M., King J W., Hewlett J S. Plasmapheresis in the treatment of thrombotic thrombocytopenic purpura. Blood 1977 50 (3) 413-417
-
(1977)
Blood
, vol.50
, Issue.3
, pp. 413-417
-
-
Bukowski, R.M.1
King, J.W.2
Hewlett, J.S.3
-
7
-
-
0025999820
-
Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients
-
Bell W R., Braine H G., Ness P M., Kickler T S. Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients. N Engl J Med 1991 325 (6) 398-403
-
(1991)
N Engl J Med
, vol.325
, Issue.6
, pp. 398-403
-
-
Bell, W.R.1
Braine, H.G.2
Ness, P.M.3
Kickler, T.S.4
-
8
-
-
0026048114
-
Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura
-
Canadian Apheresis Study Group
-
Rock G A., Shumak K H., Buskard N A. et al, Canadian Apheresis Study Group. Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. N Engl J Med 1991 325 (6) 393-397
-
(1991)
N Engl J Med
, vol.325
, Issue.6
, pp. 393-397
-
-
Rock, G.A.1
Shumak, K.H.2
Buskard, N.A.3
-
9
-
-
0023929294
-
Plasma infusion for hemolytic-uremic syndrome in children: Results of a multicenter controlled trial
-
Rizzoni G, Claris-Appiani A, Edefonti A et al. Plasma infusion for hemolytic-uremic syndrome in children: results of a multicenter controlled trial. J Pediatr 1988 112 (2) 284-290
-
(1988)
J Pediatr
, vol.112
, Issue.2
, pp. 284-290
-
-
Rizzoni, G.1
Claris-Appiani, A.2
Edefonti, A.3
-
10
-
-
0023689035
-
Treatment of the childhood haemolytic uraemic syndrome with plasma. A multicentre randomized controlled trial
-
The French Society of Paediatric Nephrology
-
Loirat C, Sonsino E, Hinglais N, Jais J P., Landais P, Fermanian J, The French Society of Paediatric Nephrology. Treatment of the childhood haemolytic uraemic syndrome with plasma. A multicentre randomized controlled trial. Pediatr Nephrol 1988 2 (3) 279-285
-
(1988)
Pediatr Nephrol
, vol.2
, Issue.3
, pp. 279-285
-
-
Loirat, C.1
Sonsino, E.2
Hinglais, N.3
Jais, J.P.4
Landais, P.5
Fermanian, J.6
-
11
-
-
58249107186
-
Interventions for hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: A systematic review of randomized controlled trials
-
Michael M, Elliott E J., Craig J C., Ridley G, Hodson E M. Interventions for hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: a systematic review of randomized controlled trials. Am J Kidney Dis 2009 53 (2) 259-272
-
(2009)
Am J Kidney Dis
, vol.53
, Issue.2
, pp. 259-272
-
-
Michael, M.1
Elliott, E.J.2
Craig, J.C.3
Ridley, G.4
Hodson, E.M.5
-
12
-
-
67049161222
-
Thrombotic microangiopathy: What not to learn from a meta-analysis
-
Noris M, Remuzzi G. Thrombotic microangiopathy: what not to learn from a meta-analysis. Nat Rev Nephrol 2009 5 (4) 186-188
-
(2009)
Nat Rev Nephrol
, vol.5
, Issue.4
, pp. 186-188
-
-
Noris, M.1
Remuzzi, G.2
-
13
-
-
0027321238
-
Plasma exchange in children with hemolytic-uremic syndrome at risk of poor outcome
-
Gianviti A, Perna A, Caringella A et al. Plasma exchange in children with hemolytic-uremic syndrome at risk of poor outcome. Am J Kidney Dis 1993 22 (2) 264-266
-
(1993)
Am J Kidney Dis
, vol.22
, Issue.2
, pp. 264-266
-
-
Gianviti, A.1
Perna, A.2
Caringella, A.3
-
14
-
-
0032443595
-
Pathophysiology and management of thrombotic microangiopathies
-
Ruggenenti P, Remuzzi G. Pathophysiology and management of thrombotic microangiopathies. J Nephrol 1998 11 (6) 300-310
-
(1998)
J Nephrol
, vol.11
, Issue.6
, pp. 300-310
-
-
Ruggenenti, P.1
Remuzzi, G.2
-
15
-
-
0024350234
-
Prolongation of acute renal failure in two patients with hemolytic-uremic syndrome due to excessive plasma infusion therapy
-
Eddy A A., Geary D F., Balfe J W., Clark W F., Baumal R. Prolongation of acute renal failure in two patients with hemolytic-uremic syndrome due to excessive plasma infusion therapy. Pediatr Nephrol 1989 3 (4) 420-423
-
(1989)
Pediatr Nephrol
, vol.3
, Issue.4
, pp. 420-423
-
-
Eddy, A.A.1
Geary, D.F.2
Balfe, J.W.3
Clark, W.F.4
Baumal, R.5
-
16
-
-
4344718851
-
Challenges in the management of infantile factor H associated hemolytic uremic syndrome
-
Filler G, Radhakrishnan S, Strain L, Hill A, Knoll G, Goodship T H. Challenges in the management of infantile factor H associated hemolytic uremic syndrome. Pediatr Nephrol 2004 19 (8) 908-911
-
(2004)
Pediatr Nephrol
, vol.19
, Issue.8
, pp. 908-911
-
-
Filler, G.1
Radhakrishnan, S.2
Strain, L.3
Hill, A.4
Knoll, G.5
Goodship, T.H.6
-
17
-
-
33847237272
-
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: Update and integration of membrane cofactor protein and Factor i mutations with structural models
-
Saunders R E., Abarrategui-Garrido C, Frémeaux-Bacchi V et al. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models. Hum Mutat 2007 28 (3) 222-234
-
(2007)
Hum Mutat
, vol.28
, Issue.3
, pp. 222-234
-
-
Saunders, R.E.1
Abarrategui-Garrido, C.2
Frémeaux-Bacchi, V.3
-
18
-
-
0027948289
-
Familial hemolytic-uremic syndrome and homozygous factor H deficiency
-
Pichette V, Quérin S, Schrch W, Brun G, Lehner-Netsch G, Delge J M. Familial hemolytic-uremic syndrome and homozygous factor H deficiency. Am J Kidney Dis 1994 24 (6) 936-941
-
(1994)
Am J Kidney Dis
, vol.24
, Issue.6
, pp. 936-941
-
-
Pichette, V.1
Quérin, S.2
Schrch, W.3
Brun, G.4
Lehner-Netsch, G.5
Delge, J.M.6
-
19
-
-
0031693194
-
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H
-
Ohali M, Shalev H, Schlesinger M et al. Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H. Pediatr Nephrol 1998 12 (8) 619-624
-
(1998)
Pediatr Nephrol
, vol.12
, Issue.8
, pp. 619-624
-
-
Ohali, M.1
Shalev, H.2
Schlesinger, M.3
-
20
-
-
0035089983
-
Familial hemolytic uremic syndrome associated with complement factor H deficiency
-
Landau D, Shalev H, Levy-Finer G, Polonsky A, Segev Y, Katchko L. Familial hemolytic uremic syndrome associated with complement factor H deficiency. J Pediatr 2001 138 (3) 412-417
-
(2001)
J Pediatr
, vol.138
, Issue.3
, pp. 412-417
-
-
Landau, D.1
Shalev, H.2
Levy-Finer, G.3
Polonsky, A.4
Segev, Y.5
Katchko, L.6
-
21
-
-
0034957282
-
Successful plasma therapy in hemolytic uremic syndrome with factor H deficiency
-
Nathanson S, Frémeaux-Bacchi V, Deschěnes G. Successful plasma therapy in hemolytic uremic syndrome with factor H deficiency. Pediatr Nephrol 2001 16 (7) 554-556
-
(2001)
Pediatr Nephrol
, vol.16
, Issue.7
, pp. 554-556
-
-
Nathanson, S.1
Frémeaux-Bacchi, V.2
Deschěnes, G.3
-
22
-
-
33748696777
-
Secondary failure of plasma therapy in factor H deficiency
-
Nathanson S, Ulinski T, Frémeaux-Bacchi V, Deschěnes G. Secondary failure of plasma therapy in factor H deficiency. Pediatr Nephrol 2006 21 (11) 1769-1771
-
(2006)
Pediatr Nephrol
, vol.21
, Issue.11
, pp. 1769-1771
-
-
Nathanson, S.1
Ulinski, T.2
Frémeaux-Bacchi, V.3
Deschěnes, G.4
-
23
-
-
20144373025
-
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
-
Licht C, Weyersberg A, Heinen S et al. 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. Am J Kidney Dis 2005 45 (2) 415-421
-
(2005)
Am J Kidney Dis
, vol.45
, Issue.2
, pp. 415-421
-
-
Licht, C.1
Weyersberg, A.2
Heinen, S.3
-
24
-
-
34247381485
-
Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
-
Cho H Y., Lee B S., Moon K C., Ha I S., Cheong H I., Choi Y. Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate. Pediatr Nephrol 2007 22 (6) 874-880
-
(2007)
Pediatr Nephrol
, vol.22
, Issue.6
, pp. 874-880
-
-
Cho, H.Y.1
Lee, B.S.2
Moon, K.C.3
Ha, I.S.4
Cheong, H.I.5
Choi, Y.6
-
25
-
-
70349673464
-
Hemolytic uremic syndrome due to homozygous factor H deficiency
-
Sethi S K., Marie-Agnes D D., Thaker N, Hari P, Bagga A. Hemolytic uremic syndrome due to homozygous factor H deficiency. Clin Exp Nephrol 2009 13 (5) 526-530
-
(2009)
Clin Exp Nephrol
, vol.13
, Issue.5
, pp. 526-530
-
-
Sethi, S.K.1
Marie-Agnes, D.D.2
Thaker, N.3
Hari, P.4
Bagga, A.5
-
26
-
-
34848903255
-
Ocular involvement in hemolytic uremic syndrome due to factor H deficiencyare there therapeutic consequences?
-
Larakeb A, Leroy S, Frémeaux-Bacchi V et al. Ocular involvement in hemolytic uremic syndrome due to factor H deficiencyare there therapeutic consequences? Pediatr Nephrol 2007 22 (11) 1967-1970
-
(2007)
Pediatr Nephrol
, vol.22
, Issue.11
, pp. 1967-1970
-
-
Larakeb, A.1
Leroy, S.2
Frémeaux-Bacchi, V.3
-
27
-
-
0036230235
-
Successful treatment of factor H-related haemolytic uraemic syndrome
-
Stratton J D., Warwicker P. Successful treatment of factor H-related haemolytic uraemic syndrome. Nephrol Dial Transplant 2002 17 (4) 684-685
-
(2002)
Nephrol Dial Transplant
, vol.17
, Issue.4
, pp. 684-685
-
-
Stratton, J.D.1
Warwicker, P.2
-
28
-
-
0141634311
-
Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormality
-
Gerber A, Kirchhoff-Moradpour A H., Obieglo S et al. Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormality. Pediatr Nephrol 2003 18 (9) 952-955
-
(2003)
Pediatr Nephrol
, vol.18
, Issue.9
, pp. 952-955
-
-
Gerber, A.1
Kirchhoff-Moradpour, A.H.2
Obieglo, S.3
-
29
-
-
47749148096
-
Plasma therapy in atypical haemolytic uremic syndrome: Lessons from a family with a factor H mutation
-
Davin J C., Strain L, Goodship T HJ. Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation. Pediatr Nephrol 2008 23 (9) 1517-1521
-
(2008)
Pediatr Nephrol
, vol.23
, Issue.9
, pp. 1517-1521
-
-
Davin, J.C.1
Strain, L.2
Goodship, T.H.3
-
30
-
-
46949105006
-
Efficacy of plasma therapy in atypical hemolytic uremic syndrome with complement factor H mutations
-
Lapeyraque A L., Wagner E, Phan V et al. Efficacy of plasma therapy in atypical hemolytic uremic syndrome with complement factor H mutations. Pediatr Nephrol 2008 23 (8) 1363-1366
-
(2008)
Pediatr Nephrol
, vol.23
, Issue.8
, pp. 1363-1366
-
-
Lapeyraque, A.L.1
Wagner, E.2
Phan, V.3
-
31
-
-
45449105770
-
Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome
-
Abarrategui-Garrido C, Melgosa M, Pea-Carrin A et al. Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome. Am J Kidney Dis 2008 52 (1) 171-180
-
(2008)
Am J Kidney Dis
, vol.52
, Issue.1
, pp. 171-180
-
-
Abarrategui-Garrido, C.1
Melgosa, M.2
Pea-Carrin, A.3
-
32
-
-
76749165686
-
Severe atypical HUS caused by CFH S1191Lcase presentation and review of treatment options
-
De S, Waters A M., Segal A O., Trautmann A, Harvey E A., Licht C. Severe atypical HUS caused by CFH S1191Lcase presentation and review of treatment options. Pediatr Nephrol 2010 25 (1) 97-104
-
(2010)
Pediatr Nephrol
, vol.25
, Issue.1
, pp. 97-104
-
-
De, S.1
Waters, A.M.2
Segal, A.O.3
Trautmann, A.4
Harvey, E.A.5
Licht, C.6
-
33
-
-
67449119124
-
The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome
-
Ferreira V P., Herbert A P., Cortés C et al. The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome. J Immunol 2009 182 (11) 7009-7018
-
(2009)
J Immunol
, vol.182
, Issue.11
, pp. 7009-7018
-
-
Ferreira, V.P.1
Herbert, A.P.2
Cortés, C.3
-
34
-
-
67651166873
-
Thrombomodulin mutations in atypical hemolytic-uremic syndrome
-
Delvaeye M, Noris M, De Vriese A et al. Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med 2009 361 (4) 345-357
-
(2009)
N Engl J Med
, vol.361
, Issue.4
, pp. 345-357
-
-
Delvaeye, M.1
Noris, M.2
De Vriese, A.3
-
35
-
-
0242331610
-
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
-
Richards A, Kemp E J., Liszewski M K. et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci U S A 2003 100 (22) 12966-12971
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.22
, pp. 12966-12971
-
-
Richards, A.1
Kemp, E.J.2
Liszewski, M.K.3
-
36
-
-
0242570482
-
Familial haemolytic uraemic syndrome and an MCP mutation
-
International Registry of Recurrent and Familial HUS/TTP
-
Noris M, Brioschi S, Caprioli J et al, International Registry of Recurrent and Familial HUS/TTP. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 2003 362 (9395) 1542-1547
-
(2003)
Lancet
, vol.362
, Issue.9395
, pp. 1542-1547
-
-
Noris, M.1
Brioschi, S.2
Caprioli, J.3
-
37
-
-
33745812440
-
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome
-
Freméaux-Bacchi V, Moulton E A., Kavanagh D et al. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome. J Am Soc Nephrol 2006 17 (7) 2017-2025
-
(2006)
J Am Soc Nephrol
, vol.17
, Issue.7
, pp. 2017-2025
-
-
Freméaux-Bacchi, V.1
Moulton, E.A.2
Kavanagh, D.3
-
38
-
-
38349172121
-
Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome
-
Fang C J., Frémeaux-Bacchi V, Liszewski M K. et al. Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome. Blood 2008 111 (2) 624-632
-
(2008)
Blood
, vol.111
, Issue.2
, pp. 624-632
-
-
Fang, C.J.1
Frémeaux-Bacchi, V.2
Liszewski, M.K.3
-
39
-
-
47149084583
-
Inherited deficiency of membrane cofactor protein expression and varying manifestations of recurrent atypical hemolytic uremic syndrome in a sibling pair
-
Couzi L, Contin-Bordes C, Marliot F et al. Inherited deficiency of membrane cofactor protein expression and varying manifestations of recurrent atypical hemolytic uremic syndrome in a sibling pair. Am J Kidney Dis 2008 52 (2) e5-e9
-
(2008)
Am J Kidney Dis
, vol.52
, Issue.2
-
-
Couzi, L.1
Contin-Bordes, C.2
Marliot, F.3
-
40
-
-
68449088805
-
Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome
-
Davin J C., Buter N, Groothoff J et al. Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome. Pediatr Nephrol 2009 24 (9) 1757-1760
-
(2009)
Pediatr Nephrol
, vol.24
, Issue.9
, pp. 1757-1760
-
-
Davin, J.C.1
Buter, N.2
Groothoff, J.3
-
41
-
-
33845513582
-
Efficacy and safety of recombinant human soluble thrombomodulin (ART-123) in disseminated intravascular coagulation: Results of a phase III, randomized, double-blind clinical trial
-
Saito H, Maruyama I, Shimazaki S et al. Efficacy and safety of recombinant human soluble thrombomodulin (ART-123) in disseminated intravascular coagulation: results of a phase III, randomized, double-blind clinical trial. J Thromb Haemost 2007 5 (1) 31-41
-
(2007)
J Thromb Haemost
, vol.5
, Issue.1
, pp. 31-41
-
-
Saito, H.1
Maruyama, I.2
Shimazaki, S.3
-
42
-
-
19444369542
-
Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome
-
Frémeaux-Bacchi V, Dragon-Durey M A., Blouin J et al. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet 2004 41 (6) e84
-
(2004)
J Med Genet
, vol.41
, Issue.6
-
-
Frémeaux-Bacchi, V.1
Dragon-Durey, M.A.2
Blouin, J.3
-
43
-
-
75749153964
-
Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome
-
Bienaimé F, Dragon-Durey M A., Regnier C H. et al. Mutations in components of complement influence the outcome of factor I-associated atypical hemolytic uremic syndrome. Kidney Int 2010 77 (4) 339-349
-
(2010)
Kidney Int
, vol.77
, Issue.4
, pp. 339-349
-
-
Bienaimé, F.1
Dragon-Durey, M.A.2
Regnier, C.H.3
-
44
-
-
27744452766
-
Mutations in complement factor i predispose to development of atypical hemolytic uremic syndrome
-
Kavanagh D, Kemp E J., Mayland E et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005 16 (7) 2150-2155
-
(2005)
J Am Soc Nephrol
, vol.16
, Issue.7
, pp. 2150-2155
-
-
Kavanagh, D.1
Kemp, E.J.2
Mayland, E.3
-
45
-
-
33751536085
-
A mutation in factor i that is associated with atypical hemolytic uremic syndrome does not affect the function of factor i in complement regulation
-
Nilsson S C., Karpman D, Vaziri-Sani F et al. A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation. Mol Immunol 2007 44 (8) 1835-1844
-
(2007)
Mol Immunol
, vol.44
, Issue.8
, pp. 1835-1844
-
-
Nilsson, S.C.1
Karpman, D.2
Vaziri-Sani, F.3
-
46
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Frémeaux-Bacchi V, Miller E C., Liszewski M K. et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood 2008 112 (13) 4948-4952
-
(2008)
Blood
, vol.112
, Issue.13
, pp. 4948-4952
-
-
Frémeaux-Bacchi, V.1
Miller, E.C.2
Liszewski, M.K.3
-
47
-
-
33846094404
-
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
-
Goicoechea de Jorge E, Harris C L., Esparza-Gordillo J et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A 2007 104 (1) 240-245
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, Issue.1
, pp. 240-245
-
-
Goicoechea De Jorge, E.1
Harris, C.L.2
Esparza-Gordillo, J.3
-
48
-
-
70350475255
-
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
-
Roumenina L T., Jablonski M, Hue C et al. Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. Blood 2009 114 (13) 2837-2845
-
(2009)
Blood
, vol.114
, Issue.13
, pp. 2837-2845
-
-
Roumenina, L.T.1
Jablonski, M.2
Hue, C.3
-
49
-
-
70349923265
-
A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure
-
Lhotta K, Janecke A R., Scheiring J et al. A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure. Clin J Am Soc Nephrol 2009 4 (8) 1356-1362
-
(2009)
Clin J Am Soc Nephrol
, vol.4
, Issue.8
, pp. 1356-1362
-
-
Lhotta, K.1
Janecke, A.R.2
Scheiring, J.3
-
50
-
-
61549117207
-
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
-
European Paediatric Study Group for HUS
-
Ariceta G, Besbas N, Johnson S et al, European Paediatric Study Group for HUS. Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome. Pediatr Nephrol 2009 24 (4) 687-696
-
(2009)
Pediatr Nephrol
, vol.24
, Issue.4
, pp. 687-696
-
-
Ariceta, G.1
Besbas, N.2
Johnson, S.3
-
51
-
-
0035722282
-
Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
-
DOI 10.1046/j.1523-1755.2001.060003831.x
-
Ruggenenti P, Noris M, Remuzzi G. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int 2001 60 (3) 831-846 (Pubitemid 34205784)
-
(2001)
Kidney International
, vol.60
, Issue.3
, pp. 831-846
-
-
Ruggenenti, P.1
Noris, M.2
Remuzzi, G.3
-
52
-
-
0038323999
-
Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias
-
Haemostasis and Thrombosis Task Force, British Committee for Standards in Haematology
-
Allford S L., Hunt B J., Rose P, Machin S J., Haemostasis and Thrombosis Task Force, British Committee for Standards in Haematology. Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias. Br J Haematol 2003 120 (4) 556-573
-
(2003)
Br J Haematol
, vol.120
, Issue.4
, pp. 556-573
-
-
Allford, S.L.1
Hunt, B.J.2
Rose, P.3
MacHin, S.J.4
-
53
-
-
72249097911
-
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom
-
working party from the Renal Association, the British Committee for Standards in Haematology and the British Transplantation Society
-
Taylor C M., Machin S, Wigmore S J., Goodship T H., working party from the Renal Association, the British Committee for Standards in Haematology and the British Transplantation Society. Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom. Br J Haematol 2010 148 (1) 37-47
-
(2010)
Br J Haematol
, vol.148
, Issue.1
, pp. 37-47
-
-
Taylor, C.M.1
MacHin, S.2
Wigmore, S.J.3
Goodship, T.H.4
-
54
-
-
34548799240
-
Complications of apheresis in children
-
Michon B, Moghrabi A, Winikoff R et al. Complications of apheresis in children. Transfusion 2007 47 (10) 1837-1842
-
(2007)
Transfusion
, vol.47
, Issue.10
, pp. 1837-1842
-
-
Michon, B.1
Moghrabi, A.2
Winikoff, R.3
-
55
-
-
56449089731
-
World apheresis registry data from 2003 to 2007, the pediatric and adolescent side of the registry
-
Witt V, Stegmayr B, Ptak J et al. World apheresis registry data from 2003 to 2007, the pediatric and adolescent side of the registry. Transfus Apheresis Sci 2008 39 (3) 255-260
-
(2008)
Transfus Apheresis Sci
, vol.39
, Issue.3
, pp. 255-260
-
-
Witt, V.1
Stegmayr, B.2
Ptak, J.3
-
56
-
-
70350130833
-
Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome
-
Chatelet V, Frémeaux-Bacchi V, Lobbedez T, Ficheux M, Hurault de Ligny B. Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome. Am J Transplant 2009 9 (11) 2644-2645
-
(2009)
Am J Transplant
, vol.9
, Issue.11
, pp. 2644-2645
-
-
Chatelet, V.1
Frémeaux-Bacchi, V.2
Lobbedez, T.3
Ficheux, M.4
Hurault De Ligny, B.5
-
57
-
-
77949570344
-
Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation
-
Davin J C., Gracchi V, Bouts A, Groothoff J, Strain L, Goodship T. Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation. Am J Kidney Dis 2010 55 (4) 708-711
-
(2010)
Am J Kidney Dis
, vol.55
, Issue.4
, pp. 708-711
-
-
Davin, J.C.1
Gracchi, V.2
Bouts, A.3
Groothoff, J.4
Strain, L.5
Goodship, T.6
-
58
-
-
59449107473
-
Eculizumab for atypical hemolytic-uremic syndrome
-
Nrnberger J, Philipp T, Witzke O et al. Eculizumab for atypical hemolytic-uremic syndrome. N Engl J Med 2009 360 (5) 542-544
-
(2009)
N Engl J Med
, vol.360
, Issue.5
, pp. 542-544
-
-
Nrnberger, J.1
Philipp, T.2
Witzke, O.3
-
59
-
-
59449088846
-
Eculizumab for congenital atypical hemolytic-uremic syndrome
-
Gruppo R A., Rother R P. Eculizumab for congenital atypical hemolytic-uremic syndrome. N Engl J Med 2009 360 (5) 544-546
-
(2009)
N Engl J Med
, vol.360
, Issue.5
, pp. 544-546
-
-
Gruppo, R.A.1
Rother, R.P.2
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