-
1
-
-
70350279315
-
Atypical hemolyticuremic syndrome
-
Noris M, Remuzzi G. Atypical hemolyticuremic 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
-
3
-
-
84863841323
-
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies
-
British Committee for Standards in Haematology
-
Scully M, Hunt BJ, Benjamin S, et al British Committee for Standards in Haematology. Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies. Br J Haematol. 2012; 158(3):323-335
-
(2012)
Br J Haematol
, vol.158
, Issue.3
, pp. 323-335
-
-
Scully, M.1
Hunt, B.J.2
Benjamin, S.3
-
4
-
-
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 (11):643-657
-
(2012)
Nat Rev Nephrol
, vol.8
, Issue.11
, pp. 643-657
-
-
Zuber, J.1
Fakhouri, F.2
Roumenina, L.T.3
Loirat, C.4
Frémeaux-Bacchi, V.5
-
5
-
-
84870161177
-
Familial atypical hemolytic uremic syndrome: A review of its genetic and clinical aspects
-
Bu F, Borsa N, Gianluigi A, Smith RJH. Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects. Clin Dev Immunol. 2012;2012:370426
-
(2012)
Clin Dev Immunol
, vol.2012
, pp. 370426
-
-
Bu, F.1
Borsa, N.2
Gianluigi, A.3
Smith, R.J.H.4
-
6
-
-
33747159590
-
Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
-
DOI 10.1182/blood-2005-10-007252
-
Caprioli J, Noris M, Brioschi S, et al. 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 (Pubitemid 44232024)
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1267-1279
-
-
Caprioli, J.1
Noris, M.2
Brioschi, S.3
Pianetti, G.4
Castelletti, F.5
Bettinaglio, P.6
Mele, C.7
Bresin, E.8
Cassis, L.9
Gamba, S.10
Porrati, F.11
Bucchioni, S.12
Monteferrante, G.13
Fang, C.J.14
Liszewski, M.K.15
Kavanagh, D.16
Atkinson, J.P.17
Remuzzi, G.18
-
7
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
Noris M, Caprioli J, Bresin E, 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(10):1844-1859
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, Issue.10
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
-
8
-
-
84879308507
-
Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation
-
Cayci FS, Cakar N, Hancer VS, Uncu N, Acar B, Gur G. Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation. Pediatr Nephrol. 2012;27(12):2327-2331
-
(2012)
Pediatr Nephrol
, vol.27
, Issue.12
, pp. 2327-2331
-
-
Cayci, F.S.1
Cakar, N.2
Hancer, V.S.3
Uncu, N.4
Acar, B.5
Gur, G.6
-
9
-
-
84868610119
-
Preservation of renal function in atypical hemolytic uremic syndrome by eculizumab: A case report
-
Giordano M, Castellano G, Messina G, et al. Preservation of renal function in atypical hemolytic uremic syndrome by eculizumab: a case report. Pediatrics. 2012;130(5):e1385-e1388
-
(2012)
Pediatrics
, vol.130
, Issue.5
-
-
Giordano, M.1
Castellano, G.2
Messina, G.3
-
10
-
-
84870411202
-
Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
-
Besbas N, Gulhan B, Karpman D, et al. Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab. Pediatr Nephrol. 2013;28(1): 155-158
-
(2013)
Pediatr Nephrol
, vol.28
, Issue.1
, pp. 155-158
-
-
Besbas, N.1
Gulhan, B.2
Karpman, D.3
-
11
-
-
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
-
12
-
-
0037103517
-
Clinical course and the role of Shiga toxin-producing Escherichia coli infection in the hemolytic-uremic syndrome in pediatric patients, 1997-2000, in Germany and Austria: A prospective study
-
DOI 10.1086/341940
-
Gerber A, Karch H, Allerberger F, Verweyen HM, Zimmerhackl LB. Clinical course and the role of Shiga toxin-producing Escherichia coli infection in the hemolytic-uremic syndrome in pediatric patients, 1997-2000, in Germany and Austria: a prospective study. J Infect Dis. 2002;186(4):493-500 (Pubitemid 34876258)
-
(2002)
Journal of Infectious Diseases
, vol.186
, Issue.4
, pp. 493-500
-
-
Gerber, A.1
Karch, H.2
Allerberger, F.3
Verweyen, H.M.4
Zimmerhackl, L.B.5
-
13
-
-
84859798441
-
Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants
-
Ariceta G, Arrizabalaga B, Aguirre M, Morteruel E, Lopez-Trascasa M. Eculizumab in the treatment of atypical hemolytic uremic syndrome in infants. Am J Kidney Dis. 2012;59(5):707-710
-
(2012)
Am J Kidney Dis
, vol.59
, Issue.5
, pp. 707-710
-
-
Ariceta, G.1
Arrizabalaga, B.2
Aguirre, M.3
Morteruel, E.4
Lopez-Trascasa, M.5
-
14
-
-
84878608990
-
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
-
Lemaire M, Frémeaux-Bacchi V, Schaefer F, et al. Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome. Nat Genet. 2013;45(5):531-536
-
(2013)
Nat Genet
, vol.45
, Issue.5
, pp. 531-536
-
-
Lemaire, M.1
Frémeaux-Bacchi, V.2
Schaefer, F.3
-
15
-
-
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(5):544-546
-
(2009)
N Engl J Med
, vol.360
, Issue.5
, pp. 544-546
-
-
Gruppo, R.A.1
Rother, R.P.2
-
16
-
-
79954433046
-
Effi cacy of eculizumab in a patient with factor-H-associated atypical hemolytic uremic syndrome
-
Lapeyraque A-L, Frémeaux-Bacchi V, Robitaille P. Effi cacy of eculizumab in a patient with factor-H-associated atypical hemolytic uremic syndrome. Pediatr Nephrol. 2011;26(4): 621-624
-
(2011)
Pediatr Nephrol
, vol.26
, Issue.4
, pp. 621-624
-
-
Lapeyraque, A.-L.1
Frémeaux-Bacchi, V.2
Robitaille, P.3
-
17
-
-
84863981911
-
Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count
-
Dorresteijn EM, van de Kar NCAJ, Cransberg K. Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count. Pediatr Nephrol. 2012;27 (7):1193-1195
-
(2012)
Pediatr Nephrol
, vol.27
, Issue.7
, pp. 1193-1195
-
-
Dorresteijn, E.M.1
Van De Kar, N.C.A.J.2
Cransberg, K.3
-
18
-
-
76749165686
-
Severe atypical HUS caused by CFH S1191L - Case presentation and review of treatment options
-
De S, Waters AM, Segal AO, Trautmann A, Harvey EA, Licht C. Severe atypical HUS caused by CFH S1191L - case 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
-
19
-
-
84878589219
-
Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
-
Legendre CM, Licht C, Muus P, et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N Engl J Med. 2013;368(23):2169-2181
-
(2013)
N Engl J Med
, vol.368
, Issue.23
, pp. 2169-2181
-
-
Legendre, C.M.1
Licht, C.2
Muus, P.3
-
20
-
-
84870534251
-
Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
-
French Study Group for Atypical HUS
-
Zuber J, Le Quintrec M, Krid S, et al French Study Group for Atypical HUS. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation. Am J Transplant. 2012;12(12):3337-3354
-
(2012)
Am J Transplant
, vol.12
, Issue.12
, pp. 3337-3354
-
-
Zuber, J.1
Le Quintrec, M.2
Krid, S.3
|