-
1
-
-
0000346272
-
Hemolytic-uremic syndrome in families
-
Kaplan B.S., Trompeter R., and Moake J. (Eds), Dekker, New York
-
Kaplan B.S., and Kaplan P. Hemolytic-uremic syndrome in families. In: Kaplan B.S., Trompeter R., and Moake J. (Eds). Hemolytic-uremic syndrome and thrombotic thrombocytopenic purpura (1992), Dekker, New York 213-225
-
(1992)
Hemolytic-uremic syndrome and thrombotic thrombocytopenic purpura
, pp. 213-225
-
-
Kaplan, B.S.1
Kaplan, P.2
-
2
-
-
0028871172
-
Haemolytic-uraemic syndrome: prognostic features in children over three years of age
-
Renaud C., Niaudet P., Gagnadoux, Broyer M., and Habib R. Haemolytic-uraemic syndrome: prognostic features in children over three years of age. Pediatr Nephrol 9 (1995) 24-29
-
(1995)
Pediatr Nephrol
, vol.9
, pp. 24-29
-
-
Renaud, C.1
Niaudet, P.2
Gagnadoux3
Broyer, M.4
Habib, R.5
-
3
-
-
0017652197
-
Haemolytic-uremic syndrome with recurrent episodes: an important subset
-
Kaplan B.S. Haemolytic-uremic syndrome with recurrent episodes: an important subset. Clin Nephrol 8 (1977) 495-498
-
(1977)
Clin Nephrol
, vol.8
, pp. 495-498
-
-
Kaplan, B.S.1
-
4
-
-
0031463774
-
Epidemic hemolytic-uremic syndrome in children
-
Repetto H.A. Epidemic hemolytic-uremic syndrome in children. Kidney Int 52 (1997) 1708-1719
-
(1997)
Kidney Int
, vol.52
, pp. 1708-1719
-
-
Repetto, H.A.1
-
5
-
-
0036947232
-
Hemolytic-uremic syndrome: epidemiology, pathophysiology, and therapy
-
Andreoli S., Trachtman H., Acheson D., Siegler R.L., and Obrig T.G. Hemolytic-uremic syndrome: epidemiology, pathophysiology, and therapy. Pediatr Nephrol 17 (2002) 293-298
-
(2002)
Pediatr Nephrol
, vol.17
, pp. 293-298
-
-
Andreoli, S.1
Trachtman, H.2
Acheson, D.3
Siegler, R.L.4
Obrig, T.G.5
-
6
-
-
5644224821
-
The role of Shiga toxin-producing Escherichia coli in hemorrhagic colitis and haemolytic-uremic syndrome
-
Cleary T.G. The role of Shiga toxin-producing Escherichia coli in hemorrhagic colitis and haemolytic-uremic syndrome. Semin Pediatr Infect Dis 15 (2004) 260-265
-
(2004)
Semin Pediatr Infect Dis
, vol.15
, pp. 260-265
-
-
Cleary, T.G.1
-
7
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake J. Thrombotic microangiopathies. N Engl J Med 347 (2002) 589-600
-
(2002)
N Engl J Med
, vol.347
, pp. 589-600
-
-
Moake, J.1
-
8
-
-
0033968804
-
Enterohemorrhagic Escherichia coli infections: following transmission routes
-
Vermelen H.M., Karch H., Brandis M., and Zimmerhackl L.B. Enterohemorrhagic Escherichia coli infections: following transmission routes. Pediatr Nephrol 14 (2000) 73-83
-
(2000)
Pediatr Nephrol
, vol.14
, pp. 73-83
-
-
Vermelen, H.M.1
Karch, H.2
Brandis, M.3
Zimmerhackl, L.B.4
-
9
-
-
0037158610
-
An outbreak of Escherichia coli O157: H7 infections among visitors to a dairy farm
-
Crump J., Sulka A., Langer A., Schaben C., Crielly A.S., Gage R., et al. An outbreak of Escherichia coli O157: H7 infections among visitors to a dairy farm. N Engl J Med 347 (2002) 555-560
-
(2002)
N Engl J Med
, vol.347
, pp. 555-560
-
-
Crump, J.1
Sulka, A.2
Langer, A.3
Schaben, C.4
Crielly, A.S.5
Gage, R.6
-
10
-
-
0034051446
-
Haemolytic-uraemic syndrome and Shiga toxin-producing Escherichia coli infection in children in France. The Société de nephrologie pediatrique
-
Decludt B., Bouvet P., Mariani-Kurkdjian P., Grimont F., Grimont P.A., Hubert B., et al. Haemolytic-uraemic syndrome and Shiga toxin-producing Escherichia coli infection in children in France. The Société de nephrologie pediatrique. Epidemiol Infect 124 (2000) 215-220
-
(2000)
Epidemiol Infect
, vol.124
, pp. 215-220
-
-
Decludt, B.1
Bouvet, P.2
Mariani-Kurkdjian, P.3
Grimont, F.4
Grimont, P.A.5
Hubert, B.6
-
11
-
-
0027343839
-
Hemolytic-uremic syndrome in the child
-
Loirat C., Baudouin V., Sonsino E., et al. Hemolytic-uremic syndrome in the child. Adv Nephrol 22 (1993) 141-168
-
(1993)
Adv Nephrol
, vol.22
, pp. 141-168
-
-
Loirat, C.1
Baudouin, V.2
Sonsino, E.3
-
12
-
-
0028130110
-
Spectrum of extrarenal involvement in postdiarrheal hemolytic-uremic syndrome
-
Siegler R. Spectrum of extrarenal involvement in postdiarrheal hemolytic-uremic syndrome. J Pediatr 125 (1994) 511-518
-
(1994)
J Pediatr
, vol.125
, pp. 511-518
-
-
Siegler, R.1
-
13
-
-
11144303331
-
Hemolytic-uremic syndromes
-
Avner E.D., Harmon W.E., and Niaudet P. (Eds), Lippincott, Williams and Wilkins, Baltimore
-
Loirat C., and Taylor C.M. Hemolytic-uremic syndromes. In: Avner E.D., Harmon W.E., and Niaudet P. (Eds). Pediatric Nephrology. 5th ed. (2003), Lippincott, Williams and Wilkins, Baltimore 887-915
-
(2003)
Pediatric Nephrology. 5th ed.
, pp. 887-915
-
-
Loirat, C.1
Taylor, C.M.2
-
14
-
-
0002394738
-
Pathology of the hemolytic and uremic syndrome
-
Kaplan B.S., Trompeter R., and Moake J. (Eds), Dekker, New York
-
Habib R. Pathology of the hemolytic and uremic syndrome. In: Kaplan B.S., Trompeter R., and Moake J. (Eds). Hemolytic-uremic syndrome and thrombotic thrombocytopenic purpura (1992), Dekker, New York 315-353
-
(1992)
Hemolytic-uremic syndrome and thrombotic thrombocytopenic purpura
, pp. 315-353
-
-
Habib, R.1
-
15
-
-
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
-
Gerber A., Karch H., Allerberger F., and Verweyen H.M. 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 186 (2002) 493-500
-
(2002)
J Infect Dis
, vol.186
, pp. 493-500
-
-
Gerber, A.1
Karch, H.2
Allerberger, F.3
Verweyen, H.M.4
-
16
-
-
0021257858
-
Hemolytic-uremic syndrome: an analysis of the natural history and prognostic features
-
Loirat C., Sonsino E., Varga Moreno A., Pillion G., Mercier J.C., Beaufils F., et al. Hemolytic-uremic syndrome: an analysis of the natural history and prognostic features. Acta Paediatr Scand 73 (1984) 505-514
-
(1984)
Acta Paediatr Scand
, vol.73
, pp. 505-514
-
-
Loirat, C.1
Sonsino, E.2
Varga Moreno, A.3
Pillion, G.4
Mercier, J.C.5
Beaufils, F.6
-
17
-
-
0031000941
-
Childhood haemolytic-uremic syndrome in Argentina: long-term follow-up and prognostic features
-
Spizzirri F., Rahman R., Bibiloni N., Ruscasso J.D., and Amoreo ORl. Childhood haemolytic-uremic syndrome in Argentina: long-term follow-up and prognostic features. Pediatr Nephrol 11 (1997) 156-160
-
(1997)
Pediatr Nephrol
, vol.11
, pp. 156-160
-
-
Spizzirri, F.1
Rahman, R.2
Bibiloni, N.3
Ruscasso, J.D.4
Amoreo, ORl.5
-
18
-
-
0027931417
-
Outcome and prognostic determinants in the haemolytic-uremic syndrome of children
-
Tönshoff B., Sammet A., Sanden I., Mehls O., Waldherr R., and Scharer K. Outcome and prognostic determinants in the haemolytic-uremic syndrome of children. Nephron 68 (1994) 63-70
-
(1994)
Nephron
, vol.68
, pp. 63-70
-
-
Tönshoff, B.1
Sammet, A.2
Sanden, I.3
Mehls, O.4
Waldherr, R.5
Scharer, K.6
-
19
-
-
0029884324
-
Long-term (15-25 years) outcome of childhood hemolytic-uremic syndrome
-
Gagnadoux M.F., Habib R., Gubler M.C., Bacri J.L., and Broyer M. Long-term (15-25 years) outcome of childhood hemolytic-uremic syndrome. Clin Nephrol 46 (1996) 39-41
-
(1996)
Clin Nephrol
, vol.46
, pp. 39-41
-
-
Gagnadoux, M.F.1
Habib, R.2
Gubler, M.C.3
Bacri, J.L.4
Broyer, M.5
-
20
-
-
0002786538
-
Prognosis of the hemolyric-uremic syndrome in children
-
Habib R., Levy M., Gagnadoux M.F., and Broyer M. Prognosis of the hemolyric-uremic syndrome in children. Adv Nephrol 11 (1982) 99-128
-
(1982)
Adv Nephrol
, vol.11
, pp. 99-128
-
-
Habib, R.1
Levy, M.2
Gagnadoux, M.F.3
Broyer, M.4
-
21
-
-
0028055099
-
Childhood haemolytic uraemic syndrome: long-term outcome and prognostic features
-
Kelles A., Van Dyck M., and Proesmans W. Childhood haemolytic uraemic syndrome: long-term outcome and prognostic features. Eur J Pediatr 153 (1994) 38-42
-
(1994)
Eur J Pediatr
, vol.153
, pp. 38-42
-
-
Kelles, A.1
Van Dyck, M.2
Proesmans, W.3
-
22
-
-
0020701017
-
Haemolytic-uraemic syndrome: an analysis of prognostic features
-
Trompeter R.S., Schwartz R., Chantler C., Dillon M.J., Haycock G.B., Kay R., et al. Haemolytic-uraemic syndrome: an analysis of prognostic features. Arch Dis Child 58 (1983) 101-105
-
(1983)
Arch Dis Child
, vol.58
, pp. 101-105
-
-
Trompeter, R.S.1
Schwartz, R.2
Chantler, C.3
Dillon, M.J.4
Haycock, G.B.5
Kay, R.6
-
23
-
-
0034729744
-
The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli 0157: H7 infections
-
Wong C.S., Jelacic S., Habeeb R.C., Watkins S.L., and Tarr Pl. The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli 0157: H7 infections. N Engl J Med 342 (2000) 1930-1936
-
(2000)
N Engl J Med
, vol.342
, pp. 1930-1936
-
-
Wong, C.S.1
Jelacic, S.2
Habeeb, R.C.3
Watkins, S.L.4
Tarr, Pl.5
-
24
-
-
33646132021
-
Development of a hybrid Shiga holotoxoid vaccine to elicit heterologous protection against Shiga toxins types 1 and 2
-
Smith M.J., Teel L.D., Carvalho H.M., Melton-Celsa A.R., and O'Brien A.D. Development of a hybrid Shiga holotoxoid vaccine to elicit heterologous protection against Shiga toxins types 1 and 2. Vaccine 24 (2006) 4122-4129
-
(2006)
Vaccine
, vol.24
, pp. 4122-4129
-
-
Smith, M.J.1
Teel, L.D.2
Carvalho, H.M.3
Melton-Celsa, A.R.4
O'Brien, A.D.5
-
25
-
-
0030777344
-
Postdysenteric haemolytic-uremic syndrome in children during an epidemic of Shigella dysentery in Kwazulu/Natal
-
Bhimma R., Rollins N.C., Coovadia H.M., and Adhikari M. Postdysenteric haemolytic-uremic syndrome in children during an epidemic of Shigella dysentery in Kwazulu/Natal. Pediatr Nephrol 11 (1997) 560-564
-
(1997)
Pediatr Nephrol
, vol.11
, pp. 560-564
-
-
Bhimma, R.1
Rollins, N.C.2
Coovadia, H.M.3
Adhikari, M.4
-
26
-
-
0036331717
-
Invasive pneumococcal disease and haemolytic-uremic syndrome
-
Brandt J., Wong C., Mihm S., Roberts J., Smith J., Brewer E., et al. Invasive pneumococcal disease and haemolytic-uremic syndrome. Pediatrics 110 (2002) 366-371
-
(2002)
Pediatrics
, vol.110
, pp. 366-371
-
-
Brandt, J.1
Wong, C.2
Mihm, S.3
Roberts, J.4
Smith, J.5
Brewer, E.6
-
27
-
-
0035061628
-
Prognosis of Streptococcus pneumoniae-induced haemolytic-uremic syndrome
-
Nathanson S., and Deschenes G. Prognosis of Streptococcus pneumoniae-induced haemolytic-uremic syndrome. Pediatr Nephrol 16 (2001) 362-365
-
(2001)
Pediatr Nephrol
, vol.16
, pp. 362-365
-
-
Nathanson, S.1
Deschenes, G.2
-
28
-
-
0027398891
-
Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood
-
Fitzpatrick M.M., Walters M.D., Trompeter R.S., Dillon M.J., and Barratt T.M. Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood. J Pediatr 122 (1993) 532-537
-
(1993)
J Pediatr
, vol.122
, pp. 532-537
-
-
Fitzpatrick, M.M.1
Walters, M.D.2
Trompeter, R.S.3
Dillon, M.J.4
Barratt, T.M.5
-
29
-
-
0030785590
-
Heterogeneity of atypical haemolytic-uremic syndromes
-
Neuhaus T.J., Calonder S., and Leumann E.P. Heterogeneity of atypical haemolytic-uremic syndromes. Arch Dis Child 76 (1997) 518-521
-
(1997)
Arch Dis Child
, vol.76
, pp. 518-521
-
-
Neuhaus, T.J.1
Calonder, S.2
Leumann, E.P.3
-
30
-
-
33747159590
-
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
-
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 108 (2006) 1267-1279
-
(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
-
31
-
-
27844566613
-
Atypical haemolytic-uraemic syndrome and mutations in complement regulator genes
-
Dragon-Durey M.A., and Fremeaux-Bacchi V. Atypical haemolytic-uraemic syndrome and mutations in complement regulator genes. Springer Semin Immunopathol 27 (2005) 359-374
-
(2005)
Springer Semin Immunopathol
, vol.27
, pp. 359-374
-
-
Dragon-Durey, M.A.1
Fremeaux-Bacchi, V.2
-
32
-
-
33847237272
-
The interactive factor H-atypical haemolytic-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., Fremeaux-Bacchi V., Goicoechea de Jorge E., Goodship T.H., Lopez Trascasa M., et al. The interactive factor H-atypical haemolytic-uremic syndrome mutation database and website: update and integration of membrane cofactor protein and factor I mutations with structural models. Hum Mutat 28 (2007) 222-234
-
(2007)
Hum Mutat
, vol.28
, pp. 222-234
-
-
Saunders, R.E.1
Abarrategui-Garrido, C.2
Fremeaux-Bacchi, V.3
Goicoechea de Jorge, E.4
Goodship, T.H.5
Lopez Trascasa, M.6
-
33
-
-
0035810399
-
Complement. First of two parts
-
Walport M.J. Complement. First of two parts. N Engl J med 344 (2001) 1058-1066
-
(2001)
N Engl J med
, vol.344
, pp. 1058-1066
-
-
Walport, M.J.1
-
34
-
-
0031970553
-
Genetic studies into haemolytic-uraemic syndrome
-
Warwicker P., Goodship T.H.J., Donne R.L., Pirson Y., Nicholls A., Ward R.M., et al. Genetic studies into haemolytic-uraemic syndrome. Kidney Int 53 (1998) 836-844
-
(1998)
Kidney Int
, vol.53
, pp. 836-844
-
-
Warwicker, P.1
Goodship, T.H.J.2
Donne, R.L.3
Pirson, Y.4
Nicholls, A.5
Ward, R.M.6
-
35
-
-
0032919054
-
Familial relapsing haemolytic-uraemic syndrome and complement factor H deficiency
-
Warwicker P., Donne R.L., Goodship J.A., Goodship T.H., Howie A.J., Kumararatne D.S., et al. Familial relapsing haemolytic-uraemic syndrome and complement factor H deficiency. Nephrol Dial Transplant 14 (1999) 1229-1233
-
(1999)
Nephrol Dial Transplant
, vol.14
, pp. 1229-1233
-
-
Warwicker, P.1
Donne, R.L.2
Goodship, J.A.3
Goodship, T.H.4
Howie, A.J.5
Kumararatne, D.S.6
-
36
-
-
0033927532
-
Complement factor H gene mutation associated with autosomal recessive atypical haemolytic-uremic syndrome
-
Buddles M.R., Donne R.L., Richards A., Goodship J., and Goodship T.H. Complement factor H gene mutation associated with autosomal recessive atypical haemolytic-uremic syndrome. Am J Hum Genet 66 (2000) 1721-1722
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1721-1722
-
-
Buddles, M.R.1
Donne, R.L.2
Richards, A.3
Goodship, J.4
Goodship, T.H.5
-
37
-
-
0035143299
-
Italian registry of familial and recurrent HUS/TTP. The molecular basis of familial haemolytic-uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
-
Caprioli J., Bettinaglio P., Zipfel P.F., Amadei B., Daina E., Gamba S., et al. Italian registry of familial and recurrent HUS/TTP. The molecular basis of familial haemolytic-uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am Soc Nephrol 12 (2001) 297-307
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 297-307
-
-
Caprioli, J.1
Bettinaglio, P.2
Zipfel, P.F.3
Amadei, B.4
Daina, E.5
Gamba, S.6
-
38
-
-
0031693194
-
Hypocomplementemic autosomal recessive haemolytic-uremic syndrome with decreased factor H
-
Ohali M., Shalev H., Schlesinger M., Katz Y., Kachko L., Carmi R., et al. Hypocomplementemic autosomal recessive haemolytic-uremic syndrome with decreased factor H. Pediatr Nephrol 12 (1998) 619-624
-
(1998)
Pediatr Nephrol
, vol.12
, pp. 619-624
-
-
Ohali, M.1
Shalev, H.2
Schlesinger, M.3
Katz, Y.4
Kachko, L.5
Carmi, R.6
-
39
-
-
0033362094
-
Complement factor H gene mutation associated with autosomal recessive atypical haemolytic-uremic syndrome
-
Ying L., Katz Y., Schlesinger M., Carmi R., Shalev H., Haider N., et al. Complement factor H gene mutation associated with autosomal recessive atypical haemolytic-uremic syndrome. Am J Hum Genet 65 (1999) 1538-1546
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1538-1546
-
-
Ying, L.1
Katz, Y.2
Schlesinger, M.3
Carmi, R.4
Shalev, H.5
Haider, N.6
-
40
-
-
0042329931
-
Haemolytic-uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries
-
Neumann H.P., Salzmann M., Bohnert-Iwan B., Mannuelian T., Skerka C., Lenk D., et al. Haemolytic-uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. J Med Genet 40 (2003) 676-681
-
(2003)
J Med Genet
, vol.40
, pp. 676-681
-
-
Neumann, H.P.1
Salzmann, M.2
Bohnert-Iwan, B.3
Mannuelian, T.4
Skerka, C.5
Lenk, D.6
-
41
-
-
27744452766
-
Mutations in complement factor I predispose to development of atypical haemolytic-uremic syndrome
-
Kavanagh D., Kemp E.J., Mayland E., Winney R.J., Duffield J.S., Warwick G., et al. Mutations in complement factor I predispose to development of atypical haemolytic-uremic syndrome. J Am Soc Nephrol 16 (2005) 2150-2155
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2150-2155
-
-
Kavanagh, D.1
Kemp, E.J.2
Mayland, E.3
Winney, R.J.4
Duffield, J.S.5
Warwick, G.6
-
42
-
-
0242570482
-
International registry of recurrent and familial HUS/TTP. Familial haemolytic-uraemic syndrome and an MCP mutation
-
Noris M., Brioschi S., Caprioli J., Todeschini M., Bresin E., Porrati F., et al. International registry of recurrent and familial HUS/TTP. Familial haemolytic-uraemic syndrome and an MCP mutation. Lancet 362 (2003) 1542-1547
-
(2003)
Lancet
, vol.362
, pp. 1542-1547
-
-
Noris, M.1
Brioschi, S.2
Caprioli, J.3
Todeschini, M.4
Bresin, E.5
Porrati, F.6
-
43
-
-
33745812440
-
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical haemolytic-uremic syndrome
-
Fremeaux-Bacchi V., Moulton E.A., Kavanagh D., Dragon-Durey M.A., Blouin J., Caudy A., et al. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical haemolytic-uremic syndrome. J Am Soc Nephrol 17 (2006) 2017-2025
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 2017-2025
-
-
Fremeaux-Bacchi, V.1
Moulton, E.A.2
Kavanagh, D.3
Dragon-Durey, M.A.4
Blouin, J.5
Caudy, A.6
-
44
-
-
33846094404
-
Gain-of-function mutations in complement factor B are associated with atypical haemolytic-uremic syndrome
-
Goicoechea de Jorge E., Harris C.L., Esparza-Gordillo J., Carreras L., Arranz E.A., Garrido C.A., et al. Gain-of-function mutations in complement factor B are associated with atypical haemolytic-uremic syndrome. Proc Natl Acad Sci USA 104 (2007) 240-245
-
(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
-
45
-
-
20544437666
-
Anti-factor H autoantibodies associated with atypical haemolytic-uremic syndrome
-
Dragon-Durey M.A., Loirat C., Cloarec S., Macher M.A., Blouin J., Nivet H., et al. Anti-factor H autoantibodies associated with atypical haemolytic-uremic syndrome. J Am Soc Nephrol 16 (2005) 555-563
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 555-563
-
-
Dragon-Durey, M.A.1
Loirat, C.2
Cloarec, S.3
Macher, M.A.4
Blouin, J.5
Nivet, H.6
-
46
-
-
0032569884
-
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
-
Furlan M., Robles R., Galbusera M., Remuzzi G., Kyrle P.A., Brenner B., et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med 339 (1998) 1578-1584
-
(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
-
47
-
-
0037015057
-
Mutations and common polymorphisms in ADAMTS 13 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 ADAMTS 13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci USA 99 (2002) 11902-11907
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 11902-11907
-
-
Kokame, K.1
Matsumoto, M.2
Soejima, K.3
Yagi, H.4
Ishizashi, H.5
Funato, M.6
-
48
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy G.G., Nichols W.C., Lian E.C., Foroud T., McClintick J.N., McGee B.M., et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 413 (2001) 488-494
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
Foroud, T.4
McClintick, J.N.5
McGee, B.M.6
-
49
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
Tsai H., and Lian E. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 339 (1998) 1585-1594
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.1
Lian, E.2
-
50
-
-
0037339175
-
Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical haemolytic-uremic syndrome
-
Veyradier A., Obert B., Haddad E., Cloarec S., Nivet H., Foulard M., et al. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical haemolytic-uremic syndrome. J Pediatr 142 (2003) 310-317
-
(2003)
J Pediatr
, vol.142
, pp. 310-317
-
-
Veyradier, A.1
Obert, B.2
Haddad, E.3
Cloarec, S.4
Nivet, H.5
Foulard, M.6
-
51
-
-
0036956049
-
Plasma therapy in von Willebrand factor-protease deficiency
-
Deschenes G., Veyradier A., Cloarec S., Benoit S., Desbois I., Gruel Y., et al. Plasma therapy in von Willebrand factor-protease deficiency. Pediatr Nephrol 17 (2002) 867-870
-
(2002)
Pediatr Nephrol
, vol.17
, pp. 867-870
-
-
Deschenes, G.1
Veyradier, A.2
Cloarec, S.3
Benoit, S.4
Desbois, I.5
Gruel, Y.6
-
53
-
-
0036250547
-
Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period
-
Kind T., Levy J., Lee M., Kaicker S., Nicholson J.F., and Kane S.A. Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period. J Pediatr Hematol Oncol 24 (2002) 327-329
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, pp. 327-329
-
-
Kind, T.1
Levy, J.2
Lee, M.3
Kaicker, S.4
Nicholson, J.F.5
Kane, S.A.6
-
54
-
-
0034566801
-
Hemolytic-uremic syndrome: hereditary forms and forms associated with hereditary diseases
-
Niaudet P., Gagnadoux M., Broyer M., et al. Hemolytic-uremic syndrome: hereditary forms and forms associated with hereditary diseases. Adv Nephrol Necker Hosp 30 (2000) 261-280
-
(2000)
Adv Nephrol Necker Hosp
, vol.30
, pp. 261-280
-
-
Niaudet, P.1
Gagnadoux, M.2
Broyer, M.3
-
55
-
-
0034113087
-
Autosomal dominant haemolytic-uremic syndrome: variable phenotypes and transplant results
-
Kaplan B., and Leonard M. Autosomal dominant haemolytic-uremic syndrome: variable phenotypes and transplant results. Pediatr Nephrol 14 (2000) 464-468
-
(2000)
Pediatr Nephrol
, vol.14
, pp. 464-468
-
-
Kaplan, B.1
Leonard, M.2
-
56
-
-
0035909844
-
Quinine-associated thrombotic thrombocytopenic purpura-hemolytic-uremic syndrome: frequency, clinical features, and long-term outcomes
-
Kojouri K., Vesely S.K., and George J.N. Quinine-associated thrombotic thrombocytopenic purpura-hemolytic-uremic syndrome: frequency, clinical features, and long-term outcomes. Ann Intern Med 135 (2001) 1047-1051
-
(2001)
Ann Intern Med
, vol.135
, pp. 1047-1051
-
-
Kojouri, K.1
Vesely, S.K.2
George, J.N.3
-
57
-
-
0036952936
-
Shiga toxin-associated haemolytic-uremic syndrome: absence of recurrence after renal transplantation
-
Ferraris J.R., Ramirez J.A., Ruiz S., Caletti M.G., Vallejo G., Piantanida J.J., et al. Shiga toxin-associated haemolytic-uremic syndrome: absence of recurrence after renal transplantation. Pediatr Nephrol 17 (2002) 809-814
-
(2002)
Pediatr Nephrol
, vol.17
, pp. 809-814
-
-
Ferraris, J.R.1
Ramirez, J.A.2
Ruiz, S.3
Caletti, M.G.4
Vallejo, G.5
Piantanida, J.J.6
-
58
-
-
0032571989
-
Recurrence of haemolytic-uremic syndrome in renal transplant recipients
-
Ducloux D., Rebibou J.M., Sernhoun-Ducloux S., Jarnali M., Fournier V., Bresson-Vautrin C., et al. Recurrence of haemolytic-uremic syndrome in renal transplant recipients. Transplantation 65 (1998) 1405-1407
-
(1998)
Transplantation
, vol.65
, pp. 1405-1407
-
-
Ducloux, D.1
Rebibou, J.M.2
Sernhoun-Ducloux, S.3
Jarnali, M.4
Fournier, V.5
Bresson-Vautrin, C.6
-
59
-
-
34548400755
-
Outcome of renal transplantation in patients with non Shiga toxin-associated haemolytic-uremic syndrome: prognostic significance of genetic backgroung
-
For the international registry of recurrent, familial HUS/TTP
-
Bresin E., Daina E., Noris M., Castelletti F., Stefanov R., Hill P., et al., For the international registry of recurrent, familial HUS/TTP. Outcome of renal transplantation in patients with non Shiga toxin-associated haemolytic-uremic syndrome: prognostic significance of genetic backgroung. Clin J Am Soc Nephrol 1 (2006) 88-89
-
(2006)
Clin J Am Soc Nephrol
, vol.1
, pp. 88-89
-
-
Bresin, E.1
Daina, E.2
Noris, M.3
Castelletti, F.4
Stefanov, R.5
Hill, P.6
-
60
-
-
39049085527
-
Récidive du syndrome hémolytique et urémique après transplantation rénale: facteurs de risque, incidence et prognostic
-
Loirat C., Sellier-Leclerc A.L., Dragon-Durey A., and Fremeaux-Bacchi V. Récidive du syndrome hémolytique et urémique après transplantation rénale: facteurs de risque, incidence et prognostic. Courrier de la Transplantation 3 (2006) 148-153
-
(2006)
Courrier de la Transplantation
, vol.3
, pp. 148-153
-
-
Loirat, C.1
Sellier-Leclerc, A.L.2
Dragon-Durey, A.3
Fremeaux-Bacchi, V.4
-
61
-
-
0242694369
-
The risk of recurrence of haemolytic-uremic syndrome after renal transplantation in children
-
Loirat C., and Niaudet P. The risk of recurrence of haemolytic-uremic syndrome after renal transplantation in children. Pediatr Nephrol 18 (2003) 1095-1101
-
(2003)
Pediatr Nephrol
, vol.18
, pp. 1095-1101
-
-
Loirat, C.1
Niaudet, P.2
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