-
1
-
-
84862783878
-
The use of ADAMTS13 activity, platelet count, and serum creatinine to differentiate acquired thrombotic thrombocytopenic purpura from other thrombotic microangiopathies
-
Cataland SR, Yang S, Wu HM. The use of ADAMTS13 activity, platelet count, and serum creatinine to differentiate acquired thrombotic thrombocytopenic purpura from other thrombotic microangiopathies. Br J Haematol 2012;157:501-3.
-
(2012)
Br J Haematol
, vol.157
, pp. 501-503
-
-
Cataland, S.R.1
Yang, S.2
Wu, H.M.3
-
2
-
-
33746508999
-
A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
-
Besbas N, Karpman D, Landau D, Loirat C, Proesmans W, Remuzzi G, et al. A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders. Kidney Int 2006;70:423-31.
-
(2006)
Kidney Int
, vol.70
, pp. 423-431
-
-
Besbas, N.1
Karpman, D.2
Landau, D.3
Loirat, C.4
Proesmans, W.5
Remuzzi, G.6
-
3
-
-
79954441390
-
Advances in our understanding of the pathogenesis of glomerular thrombotic microangiopathy
-
Keir L, Coward RJ. Advances in our understanding of the pathogenesis of glomerular thrombotic microangiopathy. Pediatr Nephrol 2011;26:523-33.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 523-533
-
-
Keir, L.1
Coward, R.J.2
-
4
-
-
84896719422
-
How i treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
-
Scully M, Goodship T. How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome. Br J Haematol 2014;164:759-66.
-
(2014)
Br J Haematol
, vol.164
, pp. 759-766
-
-
Scully, M.1
Goodship, T.2
-
5
-
-
0030973267
-
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lämmle B. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 1997;89:3097-103.
-
(1997)
Blood
, vol.89
, pp. 3097-3103
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Wassmer, M.4
Sandoz, P.5
Lämmle, B.6
-
6
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
Tsai HM, Lian EC. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 1998;339:1585-94.
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.M.1
Lian, E.C.2
-
7
-
-
0032569884
-
Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
-
Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med 1998;339:1578-84.
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Robles, R.2
Galbusera, M.3
Remuzzi, G.4
Kyrle, P.A.5
Brenner, B.6
-
8
-
-
0020657059
-
Sporadic cases of haemolytic-uraemic syndrome associated with faecal cytotoxin and cytotoxin-producing Escherichia coli in stools
-
Karmali MA, Steele BT, Petric M, Lim C. Sporadic cases of haemolytic-uraemic syndrome associated with faecal cytotoxin and cytotoxin-producing Escherichia coli in stools. Lancet 1983;1:619-20.
-
(1983)
Lancet
, vol.1
, pp. 619-620
-
-
Karmali, M.A.1
Steele, B.T.2
Petric, M.3
Lim, C.4
-
9
-
-
4143084550
-
Infection by Shiga toxin-producing Escherichia coli: An overview
-
Karmali MA. Infection by Shiga toxin-producing Escherichia coli: an overview. Mol Biotechnol 2004;26:117-22.
-
(2004)
Mol Biotechnol
, vol.26
, pp. 117-122
-
-
Karmali, M.A.1
-
10
-
-
70350693665
-
Shiga toxin activates complement and binds factor H: Evidence for an active role of complement in hemolytic uremic syndrome
-
Orth D, Khan AB, Naim A, Grif K, Brockmeyer J, Karch H, et al. Shiga toxin activates complement and binds factor H: evidence for an active role of complement in hemolytic uremic syndrome. J Immunol 2009;182:6394-400.
-
(2009)
J Immunol
, vol.182
, pp. 6394-6400
-
-
Orth, D.1
Khan, A.B.2
Naim, A.3
Grif, K.4
Brockmeyer, J.5
Karch, H.6
-
11
-
-
0041411081
-
Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: A systematic review, meta-analysis, and meta-regression
-
Garg AX, Suri RS, Barrowman N, Rehman F, Matsell D, Rosas-Arellano MP, et al. Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: a systematic review, meta-analysis, and meta-regression. J Am Med Assoc 2003;290:1360-70.
-
(2003)
J Am Med Assoc
, vol.290
, pp. 1360-1370
-
-
Garg, A.X.1
Suri, R.S.2
Barrowman, N.3
Rehman, F.4
Matsell, D.5
Rosas-Arellano, M.P.6
-
12
-
-
22544461682
-
Hemolytic uremic syndrome
-
Noris M, Remuzzi G. Hemolytic uremic syndrome. J Am Soc Nephrol 2005;16:1035-50.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 1035-1050
-
-
Noris, M.1
Remuzzi, G.2
-
13
-
-
84873723582
-
An update for atypical haemolytic uraemic syndrome: Diagnosis and treatment. A consensus document
-
Campistol JM, Arias M, Ariceta G, Blasco M, Espinosa M, Grinyó JM, et al. An update for atypical haemolytic uraemic syndrome: diagnosis and treatment. A consensus document. Nefrologia 2013;33:27-45.
-
(2013)
Nefrologia
, vol.33
, pp. 27-45
-
-
Campistol, J.M.1
Arias, M.2
Ariceta, G.3
Blasco, M.4
Espinosa, M.5
Grinyó, J.M.6
-
14
-
-
70350279315
-
Atypical hemolytic-uremic syndrome
-
Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med 2009;361:1676-87.
-
(2009)
N Engl J Med
, vol.361
, pp. 1676-1687
-
-
Noris, M.1
Remuzzi, G.2
-
15
-
-
0019387503
-
Hypocomplementaemia due to a genetic deficiency of beta 1H globulin
-
Thompson RA, Winterborn MH. Hypocomplementaemia due to a genetic deficiency of beta 1H globulin. Clin Exp Immunol 1981;46:110-9.
-
(1981)
Clin Exp Immunol
, vol.46
, pp. 110-119
-
-
Thompson, R.A.1
Winterborn, M.H.2
-
16
-
-
0031970553
-
Genetic studies into inherited and sporadic hemolytic uremic syndrome
-
Warwicker P, Goodship TH, Donne RL, Pirson Y, Nicholls A, Ward RM, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int 1998;53:836-44.
-
(1998)
Kidney Int
, vol.53
, pp. 836-844
-
-
Warwicker, P.1
Goodship, T.H.2
Donne, R.L.3
Pirson, Y.4
Nicholls, A.5
Ward, R.M.6
-
17
-
-
84906077328
-
Syndromes of thrombotic microangiopathy
-
George JN, Nester CM. Syndromes of thrombotic microangiopathy. N Engl J Med 2014;371:654-66.
-
(2014)
N Engl J Med
, vol.371
, pp. 654-666
-
-
George, J.N.1
Nester, C.M.2
-
19
-
-
84891753035
-
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome
-
Bu F, Maga T, Meyer NC, Wang K, Thomas CP, Nester CM, et al. Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome. J Am Soc Nephrol 2014;25:55-64.
-
(2014)
J Am Soc Nephrol
, vol.25
, pp. 55-64
-
-
Bu, F.1
Maga, T.2
Meyer, N.C.3
Wang, K.4
Thomas, C.P.5
Nester, C.M.6
-
20
-
-
84878608990
-
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
-
Lemaire M, Fremeaux-Bacchi V, Schaefer F, Choi M, Tang WH, Le Quintrec M, et al. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome. Nat Genet 2013;45:531-6.
-
(2013)
Nat Genet
, vol.45
, pp. 531-536
-
-
Lemaire, M.1
Fremeaux-Bacchi, V.2
Schaefer, F.3
Choi, M.4
Tang, W.H.5
Le Quintrec, M.6
-
21
-
-
84874633763
-
DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
-
Ozaltin F, Li B, Rauhauser A, An SW, Soylemezoglu O, Gonul II, et al. DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN. J Am Soc Nephrol 2013;24:377-84.
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 377-384
-
-
Ozaltin, F.1
Li, B.2
Rauhauser, A.3
An, S.W.4
Soylemezoglu, O.5
Gonul, I.I.6
-
22
-
-
74049164674
-
Genotype-phenotype correlation in congenital ADAMTS13 deficient patients
-
Lotta LA, Garagiola I, Cairo A. Genotype-phenotype correlation in congenital ADAMTS13 deficient patients. Blood 2008;112:Abstract 273.
-
(2008)
Blood
, vol.112
, pp. 273
-
-
Lotta, L.A.1
Garagiola, I.2
Cairo, A.3
-
23
-
-
59449089457
-
Inherited thrombotic thrombocytopenic purpura
-
Galbusera M, Noris M, Remuzzi G. Inherited thrombotic thrombocytopenic purpura. Haematologica 2009;94:166-70.
-
(2009)
Haematologica
, vol.94
, pp. 166-170
-
-
Galbusera, M.1
Noris, M.2
Remuzzi, G.3
-
24
-
-
80955168000
-
Epidemic profile of Shigatoxin-producing Escherichia coli O104:H4 outbreak in Germany
-
HUS Investigation Team
-
Frank C, Werber D, Cramer JP, Askar M, Faber M, an der Heiden M, et al.; HUS Investigation Team. Epidemic profile of Shigatoxin-producing Escherichia coli O104:H4 outbreak in Germany. N Engl J Med 2011;365:1771-80.
-
(2011)
N Engl J Med
, vol.365
, pp. 1771-1780
-
-
Frank, C.1
Werber, D.2
Cramer, J.P.3
Askar, M.4
Faber, M.5
An Der Heiden, M.6
-
25
-
-
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, Pianetti G, Castelletti F, Bettinaglio P, 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;108:1267-79.
-
(2006)
Blood
, vol.108
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
Pianetti, G.4
Castelletti, F.5
Bettinaglio, P.6
-
26
-
-
33846094404
-
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
-
Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J, Carreras L, Arranz EA, Garrido CA, et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci USA 2007;104:240-5.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 240-245
-
-
Goicoechea De Jorge, E.1
Harris, C.L.2
Esparza-Gordillo, J.3
Carreras, L.4
Arranz, E.A.5
Garrido, C.A.6
-
27
-
-
54049137505
-
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
-
Fremeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood 2008;112:4948-52.
-
(2008)
Blood
, vol.112
, pp. 4948-4952
-
-
Fremeaux-Bacchi, V.1
Miller, E.C.2
Liszewski, M.K.3
Strain, L.4
Blouin, J.5
Brown, A.L.6
-
28
-
-
34547633064
-
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
-
French Society of Pediatric Nephrology
-
Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, 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;18:2392-400.
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2392-2400
-
-
Sellier-Leclerc, A.L.1
Fremeaux-Bacchi, V.2
Dragon-Durey, M.A.3
Macher, M.A.4
Niaudet, P.5
Guest, G.6
-
29
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 2010;5:1844-59.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
Mossali, C.4
Pianetti, G.5
Gamba, S.6
-
30
-
-
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, Karpman D, Landau D, Licht C, et al.; European Paediatric Study Group for HUS. Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome. Pediatr Nephrol 2009;24:687-96.
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 687-696
-
-
Ariceta, G.1
Besbas, N.2
Johnson, S.3
Karpman, D.4
Landau, D.5
Licht, C.6
-
31
-
-
0002978048
-
Hyaline thrombosis of the terminal arterioles and capillaries: A hitherto undescribed disease
-
Moschcowitz E. Hyaline thrombosis of the terminal arterioles and capillaries: a hitherto undescribed disease. Proc N Y Pathol Soc 1924;24:21-4.
-
(1924)
Proc N y Pathol Soc
, vol.24
, pp. 21-24
-
-
Moschcowitz, E.1
-
32
-
-
0037015057
-
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
-
Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, et al. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci U S A 2002;99:11902-7.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 11902-11907
-
-
Kokame, K.1
Matsumoto, M.2
Soejima, K.3
Yagi, H.4
Ishizashi, H.5
Funato, M.6
-
33
-
-
79960635121
-
Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan
-
Fujimura Y, Matsumoto M, Isonishi A, Yagi H, Kokame K, Soejima K, et al. Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan. J Thromb Haemost 2011;9(Suppl 1):283-301.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 283-301
-
-
Fujimura, Y.1
Matsumoto, M.2
Isonishi, A.3
Yagi, H.4
Kokame, K.5
Soejima, K.6
-
34
-
-
0037372508
-
Von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP
-
Schneppenheim R, Budde U, Oyen F, Angerhaus D, Aumann V, Drewke E, et al. von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Blood 2003;101: 1845-50.
-
(2003)
Blood
, vol.101
, pp. 1845-1850
-
-
Schneppenheim, R.1
Budde, U.2
Oyen, F.3
Angerhaus, D.4
Aumann, V.5
Drewke, E.6
-
35
-
-
84906806362
-
Management of thrombotic thrombocytopenic purpura: Current perspectives
-
Blombery P, Scully M. Management of thrombotic thrombocytopenic purpura: current perspectives. J Blood Med 2014;5:15-23.
-
(2014)
J Blood Med
, vol.5
, pp. 15-23
-
-
Blombery, P.1
Scully, M.2
-
36
-
-
48749102188
-
Regional UK TTP registry: Correlation with laboratory ADAMTS 13 analysis and clinical features
-
Scully M, Yarranton H, Liesner R, Cavenagh J, Hunt B, Benjamin S, et al. Regional UK TTP registry: correlation with laboratory ADAMTS 13 analysis and clinical features. Br J Haematol 2008;142:819-26.
-
(2008)
Br J Haematol
, vol.142
, pp. 819-826
-
-
Scully, M.1
Yarranton, H.2
Liesner, R.3
Cavenagh, J.4
Hunt, B.5
Benjamin, S.6
-
37
-
-
84936619463
-
Thrombotic thrombocytopenic purpura: Report of 16 cases and review of the literature
-
Amorosi EL, Ultmann JE. Thrombotic thrombocytopenic purpura: report of 16 cases and review of the literature. Medicine 1966;45:139-59.
-
(1966)
Medicine
, vol.45
, pp. 139-159
-
-
Amorosi, E.L.1
Ultmann, J.E.2
-
38
-
-
0001478161
-
Hemolytic-uremic syndrome: Bilateral necrosis of the renal cortex in acute acquired hemolytic anemia
-
Gasser C, Gautier E, Steck A, Siebenmann RE, Oechslin R. Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia. Schweiz Med Wochenschr 1955;85:905-9.
-
(1955)
Schweiz Med Wochenschr
, vol.85
, pp. 905-909
-
-
Gasser, C.1
Gautier, E.2
Steck, A.3
Siebenmann, R.E.4
Oechslin, R.5
-
39
-
-
0023787493
-
The histopathology of the hemolytic uremic syndrome associated with verocytotoxin-producing Escherichia coli infections
-
Richardson SE, Karmali MA, Becker LE, Smith CR. The histopathology of the hemolytic uremic syndrome associated with verocytotoxin-producing Escherichia coli infections. Hum Pathol 1988;19:1102-8.
-
(1988)
Hum Pathol
, vol.19
, pp. 1102-1108
-
-
Richardson, S.E.1
Karmali, M.A.2
Becker, L.E.3
Smith, C.R.4
-
40
-
-
17144365102
-
Hemolytic uremic syndrome; Pathogenesis, treatment, and outcome
-
Siegler R, Oakes R. Hemolytic uremic syndrome; pathogenesis, treatment, and outcome. Curr Opin Pediatr 2005;17:200-4.
-
(2005)
Curr Opin Pediatr
, vol.17
, pp. 200-204
-
-
Siegler, R.1
Oakes, R.2
-
41
-
-
33646841147
-
Predictors of fatality in postdiarrheal hemolytic uremic syndrome
-
Oakes RS, Siegler RL, McReynolds MA, Pysher T, Pavia AT. Predictors of fatality in postdiarrheal hemolytic uremic syndrome. Pediatrics 2006;117:1656-62.
-
(2006)
Pediatrics
, vol.117
, pp. 1656-1662
-
-
Oakes, R.S.1
Siegler, R.L.2
McReynolds, M.A.3
Pysher, T.4
Pavia, A.T.5
-
42
-
-
50949103794
-
Surveillance of hemolytic uremic syndrome in children less than 15 years of age, a system to monitor O157 and non-O157 Shiga toxin-producing Escherichia coli infections in France, 1996-2006
-
Espie E, Grimont F, Mariani-Kurkdjian P, Bouvet P, Haeghebaert S, Filliol I, et al. Surveillance of hemolytic uremic syndrome in children less than 15 years of age, a system to monitor O157 and non-O157 Shiga toxin-producing Escherichia coli infections in France, 1996-2006. Pediatr Infect Dis J 2008;27:595-601.
-
(2008)
Pediatr Infect Dis J
, vol.27
, pp. 595-601
-
-
Espie, E.1
Grimont, F.2
Mariani-Kurkdjian, P.3
Bouvet, P.4
Haeghebaert, S.5
Filliol, I.6
-
43
-
-
0035478387
-
The central Scotland Escherichia coli O157:H7 outbreak: Risk factors for the hemolytic uremic syndrome and death among hospitalized patients
-
Dundas S, Todd WT, Stewart AI, Murdoch PS, Chaudhuri AK, Hutchinson SJ. The central Scotland Escherichia coli O157:H7 outbreak: risk factors for the hemolytic uremic syndrome and death among hospitalized patients. Clin Infect Dis 2001;33:923-31.
-
(2001)
Clin Infect Dis
, vol.33
, pp. 923-931
-
-
Dundas, S.1
Todd, W.T.2
Stewart, A.I.3
Murdoch, P.S.4
Chaudhuri, A.K.5
Hutchinson, S.J.6
-
44
-
-
77956228365
-
Chronic renal disease is more prevalent in patients with hemolytic uremic syndrome who had a positive history of diarrhea
-
Sharma AP, Filler G, Dwight P, Clark WF. Chronic renal disease is more prevalent in patients with hemolytic uremic syndrome who had a positive history of diarrhea. Kidney Int 2010;78:598-604.
-
(2010)
Kidney Int
, vol.78
, pp. 598-604
-
-
Sharma, A.P.1
Filler, G.2
Dwight, P.3
Clark, W.F.4
-
45
-
-
2542420109
-
Non-enteropathic hemolytic uremic syndrome: Causes and short-term course
-
Constantinescu AR, Bitzan M, Weiss LS, Christen E, Kaplan BS, Cnaan A, et al. Non-enteropathic hemolytic uremic syndrome: causes and short-term course. Am J Kidney Dis 2004;43: 976-82.
-
(2004)
Am J Kidney Dis
, vol.43
, pp. 976-982
-
-
Constantinescu, A.R.1
Bitzan, M.2
Weiss, L.S.3
Christen, E.4
Kaplan, B.S.5
Cnaan, A.6
-
46
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A, Bienaimé F, Dragon-Durey MA, Ngo S, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol 2013;8:554-62.
-
(2013)
Clin J Am Soc Nephrol
, vol.8
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
Bienaimé, F.4
Dragon-Durey, M.A.5
Ngo, S.6
-
47
-
-
0344624868
-
The pathogenesis and treatment of hemolytic uremic syndrome
-
Kaplan BS, Meyers KE, Schulman SL. The pathogenesis and treatment of hemolytic uremic syndrome. J Am Soc Nephrol 1998;9:1126-33.
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 1126-1133
-
-
Kaplan, B.S.1
Meyers, K.E.2
Schulman, S.L.3
-
48
-
-
84870534251
-
Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
-
French Study Group for Atypical HUS
-
Zuber J, Le Quintrec M, Krid S, Bertoye C, Gueutin V, Lahoche A, et al.; French Study Group for Atypical HUS. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation. Am J Transplant 2012;12:3337-54.
-
(2012)
Am J Transplant
, vol.12
, pp. 3337-3354
-
-
Zuber, J.1
Le Quintrec, M.2
Krid, S.3
Bertoye, C.4
Gueutin, V.5
Lahoche, A.6
-
49
-
-
84944077804
-
Extra-renal manifestations of complement-mediated thrombotic microangiopathies
-
Hofer J, Rosales A, Fischer C, Giner T. Extra-renal manifestations of complement-mediated thrombotic microangiopathies. Front Pediatr 2014;2:97.
-
(2014)
Front Pediatr
, vol.2
, pp. 97
-
-
Hofer, J.1
Rosales, A.2
Fischer, C.3
Giner, T.4
-
50
-
-
84883557853
-
Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Clinically differentiating the thrombotic microangiopathies
-
Cataland SR, Wu HM. Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: clinically differentiating the thrombotic microangiopathies. Eur J Intern Med 2013;24:486-91.
-
(2013)
Eur J Intern Med
, vol.24
, pp. 486-491
-
-
Cataland, S.R.1
Wu, H.M.2
-
51
-
-
77956532403
-
Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: The French TMA reference center experience
-
French Reference Center for Thrombotic Microangiopathies
-
Coppo P, Schwarzinger M, Buffet M, Wynckel A, Clabault K, Presne C, et al.; French Reference Center for Thrombotic Microangiopathies. Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience. PLoS One 2010;5:e10208.
-
(2010)
PLoS One
, vol.5
, pp. e10208
-
-
Coppo, P.1
Schwarzinger, M.2
Buffet, M.3
Wynckel, A.4
Clabault, K.5
Presne, C.6
-
52
-
-
84867993256
-
Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
-
French Study Group for aHUS/C3G
-
Zuber J, Fakhouri F, Roumenina LT, Loirat C, Frémeaux-Bacchi V; French Study Group for aHUS/C3G. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat Rev Nephrol 2012;8:643-57.
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 643-657
-
-
Zuber, J.1
Fakhouri, F.2
Roumenina, L.T.3
Loirat, C.4
Frémeaux-Bacchi, V.5
-
53
-
-
77949903692
-
Survival and relapse in patients with thrombotic thrombocytopenic purpura
-
Kremer Hovinga JA, Vesely SK, Terrell DR, Lammle B, George JN. Survival and relapse in patients with thrombotic thrombocytopenic purpura. Blood 2010;115:1500-11.
-
(2010)
Blood
, vol.115
, pp. 1500-1511
-
-
Kremer Hovinga, J.A.1
Vesely, S.K.2
Terrell, D.R.3
Lammle, B.4
George, J.N.5
-
54
-
-
84880799517
-
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
-
Wong EK, Goodship TH, Kavanagh D. Complement therapy in atypical haemolytic uraemic syndrome (aHUS). Mol Immunol 2013;56:199-212.
-
(2013)
Mol Immunol
, vol.56
, pp. 199-212
-
-
Wong, E.K.1
Goodship, T.H.2
Kavanagh, D.3
-
55
-
-
84906556500
-
Cardiovascular complications in atypical haemolytic uraemic syndrome
-
Noris M, Remuzzi G. Cardiovascular complications in atypical haemolytic uraemic syndrome. Nat Rev Nephrol 2014;10: 174-80.
-
(2014)
Nat Rev Nephrol
, vol.10
, pp. 174-180
-
-
Noris, M.1
Remuzzi, G.2
-
56
-
-
84908611206
-
Dynamics of complement activation in aHUS and how to monitor eculizumab therapy
-
Noris M, Galbusera M, Gastoldi S, Macor P, Banterla F, Bresin E, et al. Dynamics of complement activation in aHUS and how to monitor eculizumab therapy. Blood 2014;124:1715-26.
-
(2014)
Blood
, vol.124
, pp. 1715-1726
-
-
Noris, M.1
Galbusera, M.2
Gastoldi, S.3
Macor, P.4
Banterla, F.5
Bresin, E.6
-
57
-
-
59449088846
-
Eculizumab for congenital atypical hemolytic-uremic syndrome
-
Gruppo RA, Rother RP. Eculizumab for congenital atypical hemolytic-uremic syndrome. N Engl J Med 2009;360:544-6.
-
(2009)
N Engl J Med
, vol.360
, pp. 544-546
-
-
Gruppo, R.A.1
Rother, R.P.2
-
58
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre CM, Licht C, Muus P, Greenbaum LA, Babu S, Bedrosian C, et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med 2013;368:2169-81.
-
(2013)
N Engl J Med
, vol.368
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
Greenbaum, L.A.4
Babu, S.5
Bedrosian, C.6
-
59
-
-
84892576159
-
Eculizumab (ECU) inhibits thrombotic microangiopathy (TMA) and improves renal function in pediatric atypical hemolytic uremic syndrome (aHUS) patients (pts)
-
Atlanta, Ga., November 9, Abstract SA-PO849
-
Greenbaum LA, Fila M, Tsimaratos M. Eculizumab (ECU) inhibits thrombotic microangiopathy (TMA) and improves renal function in pediatric atypical hemolytic uremic syndrome (aHUS) patients (pts). Presented at American Society of Nephrology (ASN) Kidney Week 2013, Atlanta, Ga., November 9, 2013. Abstract SA-PO849.
-
(2013)
American Society of Nephrology (ASN) Kidney Week 2013
-
-
Greenbaum, L.A.1
Fila, M.2
Tsimaratos, M.3
-
60
-
-
84944105956
-
Eculizumab (ECU) inhibits thrombotic microangiopathy (TMA) and improves renal function in adult patients (pts) with atypical hemolytic uremic syndrome (aHUS)
-
Atlanta, Ga., November 8, 2013. Abstract FR-OR057
-
Fakhouri F, Hourmant M, Campistol JM. Eculizumab (ECU) inhibits thrombotic microangiopathy (TMA) and improves renal function in adult patients (pts) with atypical hemolytic uremic syndrome (aHUS). Presented at American Society of Nephrol ogy (ASN) Kidney Week 2013, Atlanta, Ga., November 8, 2013. Abstract FR-OR057.
-
(2013)
American Society of Nephrol Ogy (ASN) Kidney Week
-
-
Fakhouri, F.1
Hourmant, M.2
Campistol, J.M.3
-
61
-
-
84892579246
-
Eculizumab: A review of its use in atypical haemolytic uraemic syndrome
-
Keating GM. Eculizumab: a review of its use in atypical haemolytic uraemic syndrome. Drugs 2013;73:2053-66.
-
(2013)
Drugs
, vol.73
, pp. 2053-2066
-
-
Keating, G.M.1
-
62
-
-
84944105957
-
Increased understanding of atypical haemolytic uraemic syndrome (aHUS): Characteristics of patients recruited into the global aHUS registry
-
[Epub ahead of print]
-
Vande Walle J, Johnson S, Fremeaux-Bacchi V. Increased understanding of atypical haemolytic uraemic syndrome (aHUS): characteristics of patients recruited into the global aHUS registry. Nephrol Dial Transplant 2014. [Epub ahead of print].
-
(2014)
Nephrol Dial Transplant
-
-
Vande Walle, J.1
Johnson, S.2
Fremeaux-Bacchi, V.3
-
63
-
-
58249107188
-
Recurrent atypical hemolytic uremic syndrome associated with factor i mutation in a living related renal transplant recipient
-
Chan MR, Thomas CP, Torrealba JR, Djamali A, Fernandez LA, Nishimura CJ, et al. Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient. Am J Kidney Dis 2009;53:321-6.
-
(2009)
Am J Kidney Dis
, vol.53
, pp. 321-326
-
-
Chan, M.R.1
Thomas, C.P.2
Torrealba, J.R.3
Djamali, A.4
Fernandez, L.A.5
Nishimura, C.J.6
-
64
-
-
84894107600
-
Liver-kidney transplantation to cure atypical HUS: Still an option post-eculizumab?
-
Saland J. Liver-kidney transplantation to cure atypical HUS: still an option post-eculizumab? Pediatr Nephrol 2014;29:329-32.
-
(2014)
Pediatr Nephrol
, vol.29
, pp. 329-332
-
-
Saland, J.1
-
65
-
-
77954048044
-
Thrombotic microangiopathy after kidney transplantation
-
Noris M, Remuzzi G. Thrombotic microangiopathy after kidney transplantation. Am J Transplant 2010;10:1517-23.
-
(2010)
Am J Transplant
, vol.10
, pp. 1517-1523
-
-
Noris, M.1
Remuzzi, G.2
-
66
-
-
84874417661
-
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome
-
Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A, et al. Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome. Am J Transplant 2013;13: 663-75.
-
(2013)
Am J Transplant
, vol.13
, pp. 663-675
-
-
Le Quintrec, M.1
Zuber, J.2
Moulin, B.3
Kamar, N.4
Jablonski, M.5
Lionet, A.6
-
67
-
-
84884821706
-
Targeted strategies in the prevention and management of atypical HUS recurrence after kidney transplantation
-
Zuber J, Le Quintrec M, Morris H, Frémeaux-Bacchi V, Loirat C, Legendre C. Targeted strategies in the prevention and management of atypical HUS recurrence after kidney transplantation. Transplant Rev (Orlando) 2013;27:117-25.
-
(2013)
Transplant Rev (Orlando)
, vol.27
, pp. 117-125
-
-
Zuber, J.1
Le Quintrec, M.2
Morris, H.3
Frémeaux-Bacchi, V.4
Loirat, C.5
Legendre, C.6
-
68
-
-
68449088805
-
Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome
-
Davin JC, Buter N, Groothoff J, van Wijk J, Bouts A, Strain L, et al. Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome. Pediatr Nephrol 2009;24:1757-60.
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1757-1760
-
-
Davin, J.C.1
Buter, N.2
Groothoff, J.3
Van Wijk, J.4
Bouts, A.5
Strain, L.6
|