-
1
-
-
0021858462
-
Immunohistochemistry of vascular lesion in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen
-
Asada Y, Sumiyoshi A, Hayashi T, Suzumiya J, Kaketani K. Immunohistochemistry of vascular lesion in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen. Thromb Res 1985;38:469-479
-
(1985)
Thromb Res
, vol.38
, pp. 469-479
-
-
Asada, Y.1
Sumiyoshi, A.2
Hayashi, T.3
Suzumiya, J.4
Kaketani, K.5
-
2
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake JL. Thrombotic microangiopathies. N Engl J Med 2002;347:589-600
-
(2002)
N Engl J Med
, vol.347
, pp. 589-600
-
-
Moake, J.L.1
-
3
-
-
0001478161
-
Hemolytic-uremic syndrome: Bilateral necrosis of the renal cortex in acute acquired hemolytic anemia [in German]
-
Gasser C, Gautier E, Steck A, Siebenmann RE, Oechslin R. Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia [in German]. Schweiz Med Wochenschr 1995;85:905-909
-
(1995)
Schweiz Med Wochenschr
, vol.85
, pp. 905-909
-
-
Gasser, C.1
Gautier, E.2
Steck, A.3
Siebenmann, R.E.4
Oechslin, R.5
-
4
-
-
20144386770
-
Childhood hemolytic uremic syndrome, United Kingdom and Ireland
-
Lynn RM, O'Brien SJ, Taylor CM, et al. Childhood hemolytic uremic syndrome, United Kingdom and Ireland. Emerg Infect Dis 2005;11:590-596
-
(2005)
Emerg Infect Dis
, vol.11
, pp. 590-596
-
-
Lynn, R.M.1
O'Brien, S.J.2
Taylor, C.M.3
-
5
-
-
17144365102
-
Hemolytic uremic syndrome; pathogenesis, treatment, and outcome
-
Siegler R, Oakes R. Hemolytic uremic syndrome; pathogenesis, treatment, and outcome. Curr Opin Pediatr 2005; 17:200-204
-
(2005)
Curr Opin Pediatr
, vol.17
, pp. 200-204
-
-
Siegler, R.1
Oakes, R.2
-
7
-
-
0020662906
-
Escherichia coli O157:H7 strains associated with haemorrhagic colitis in the United States produce a Shigella dysenteriae 1 (SHIGA) like cytotoxin
-
O'Brien AO, Lively TA, Chen ME, Rothman SW, Formal SB. Escherichia coli O157:H7 strains associated with haemorrhagic colitis in the United States produce a Shigella dysenteriae 1 (SHIGA) like cytotoxin. Lancet 1983;1:702
-
(1983)
Lancet
, vol.1
, pp. 702
-
-
O'Brien, A.O.1
Lively, T.A.2
Chen, M.E.3
Rothman, S.W.4
Formal, S.B.5
-
8
-
-
0035312984
-
The United States National Prospective Hemolytic Uremic Syndrome Study: Microbiologic, serologic, clinical, and epidemiologic findings
-
Banatvala N, Griffin PM, Greene KD, et al. The United States National Prospective Hemolytic Uremic Syndrome Study: microbiologic, serologic, clinical, and epidemiologic findings. J Infect Dis 2001;183:1063-1070
-
(2001)
J Infect Dis
, vol.183
, pp. 1063-1070
-
-
Banatvala, N.1
Griffin, P.M.2
Greene, K.D.3
-
9
-
-
0025293858
-
Haemolytic uraemic syndromes in the British Isles 1985-8: Association with verocytotoxin producing Escherichia coli. Part 1: Clinical and epidemiological aspects
-
Milford DV, Taylor CM, Guttridge B, et al. Haemolytic uraemic syndromes in the British Isles 1985-8: association with verocytotoxin producing Escherichia coli. Part 1: clinical and epidemiological aspects. Arch Dis Child 1990;65:716-721
-
(1990)
Arch Dis Child
, vol.65
, pp. 716-721
-
-
Milford, D.V.1
Taylor, C.M.2
Guttridge, B.3
-
10
-
-
0025375397
-
Haemolytic uraemic syndromes in the British Isles, 1985-8: Association with verocytotoxin producing Escherichia coli. Part 2: Microbiological aspects
-
Kleanthous H, Smith HR, Scotland SM, et al. Haemolytic uraemic syndromes in the British Isles, 1985-8: association with verocytotoxin producing Escherichia coli. Part 2: microbiological aspects. Arch Dis Child 1990;65:722-727
-
(1990)
Arch Dis Child
, vol.65
, pp. 722-727
-
-
Kleanthous, H.1
Smith, H.R.2
Scotland, S.M.3
-
11
-
-
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, 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;186:493-500
-
(2002)
J Infect Dis
, vol.186
, pp. 493-500
-
-
Gerber, A.1
Karch, H.2
Allerberger, F.3
Verweyen, H.M.4
Zimmerhackl, L.B.5
-
12
-
-
0037242468
-
Shiga toxin-producing Escherichia coli infections associated with hemolytic uremic syndrome, Italy, 1988-2000
-
Tozzi AE, Caprioli A, Minelli F, et al. Shiga toxin-producing Escherichia coli infections associated with hemolytic uremic syndrome, Italy, 1988-2000. Emerg Infect Dis 2003;9:106-108
-
(2003)
Emerg Infect Dis
, vol.9
, pp. 106-108
-
-
Tozzi, A.E.1
Caprioli, A.2
Minelli, F.3
-
13
-
-
0034922033
-
Nationwide study of haemolytic uraemic syndrome: Clinical, microbiological, and epidemiological features
-
Elliott EJ, Robins-Browne RM, O'Loughlin EV, et al. Nationwide study of haemolytic uraemic syndrome: clinical, microbiological, and epidemiological features. Arch Dis Child 2001;85:125-131
-
(2001)
Arch Dis Child
, vol.85
, pp. 125-131
-
-
Elliott, E.J.1
Robins-Browne, R.M.2
O'Loughlin, E.V.3
-
14
-
-
0005500424
-
Surveillance of haemolytic uraemic syndrome in children under 15 years of age in France in 1998
-
Haeghebaert S, Vaillant V, Decludt B, Grimont PA. Surveillance of haemolytic uraemic syndrome in children under 15 years of age in France in 1998. Euro Surveill 2000;5:68-73
-
(2000)
Euro Surveill
, vol.5
, pp. 68-73
-
-
Haeghebaert, S.1
Vaillant, V.2
Decludt, B.3
Grimont, P.A.4
-
15
-
-
0345373923
-
Cluster of hemolytic-uremic syndrome caused by Shiga toxin-producing Escherichia coli O26:H11
-
Misselwitz J, Karch H, Bielazewska M, et al. Cluster of hemolytic-uremic syndrome caused by Shiga toxin-producing Escherichia coli O26:H11. Pediatr Infect Dis J 2003;22:349-354
-
(2003)
Pediatr Infect Dis J
, vol.22
, pp. 349-354
-
-
Misselwitz, J.1
Karch, H.2
Bielazewska, M.3
-
16
-
-
0345293129
-
An outbreak of Escherichia coli O157 infection following exposure to a contaminated building
-
Varma JK, Greene KD, Reller ME, et al. An outbreak of Escherichia coli O157 infection following exposure to a contaminated building. JAMA 2003;290:2709-2712
-
(2003)
JAMA
, vol.290
, pp. 2709-2712
-
-
Varma, J.K.1
Greene, K.D.2
Reller, M.E.3
-
17
-
-
0343953051
-
Binding and transfer of verocytotoxin by polymorphonuclear leukocytes in hemolytic uremic syndrome
-
te Loo DM, Monnens LA, Der Velden TJ, et al. Binding and transfer of verocytotoxin by polymorphonuclear leukocytes in hemolytic uremic syndrome. Blood 2000;95:3396-3402
-
(2000)
Blood
, vol.95
, pp. 3396-3402
-
-
Te Loo, D.M.1
Monnens, L.A.2
Der Velden, T.J.3
-
18
-
-
0035874529
-
Platelet activation by Shiga toxin and circulatory factors as a pathogenetic mechanism in the hemolytic uremic syndrome
-
Karpman D, Papadopoulou D, Nilsson K, et al. Platelet activation by Shiga toxin and circulatory factors as a pathogenetic mechanism in the hemolytic uremic syndrome. Blood 2001;97:3100-3108
-
(2001)
Blood
, vol.97
, pp. 3100-3108
-
-
Karpman, D.1
Papadopoulou, D.2
Nilsson, K.3
-
19
-
-
0034978873
-
The role of virulence factors in enterohemorrhagic Escherichia coli (EHEC)-associated hemolytic-uremic syndrome
-
Karch H. The role of virulence factors in enterohemorrhagic Escherichia coli (EHEC)-associated hemolytic-uremic syndrome. Semin Thromb Hemost 2001;27:207-213
-
(2001)
Semin Thromb Hemost
, vol.27
, pp. 207-213
-
-
Karch, H.1
-
20
-
-
0036707878
-
Molecular basis for high renal cell sensitivity to the cytotoxic effects of shigatoxin-1: Upregulation of globotriaosylceramide expression
-
Hughes AK, Ergonul Z, Stricklett PK, Kohan DE. Molecular basis for high renal cell sensitivity to the cytotoxic effects of shigatoxin-1: upregulation of globotriaosylceramide expression. J Am Soc Nephrol 2002;13:2239-2245
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 2239-2245
-
-
Hughes, A.K.1
Ergonul, Z.2
Stricklett, P.K.3
Kohan, D.E.4
-
21
-
-
0032962143
-
The detection of Shiga toxins in the kidney of a patient with hemolytic uremic syndrome
-
Uchida H, Kiyokawa N, Horie H, Fujimoto J, Takeda T. The detection of Shiga toxins in the kidney of a patient with hemolytic uremic syndrome. Pediatr Res 1999;45:133-137
-
(1999)
Pediatr Res
, vol.45
, pp. 133-137
-
-
Uchida, H.1
Kiyokawa, N.2
Horie, H.3
Fujimoto, J.4
Takeda, T.5
-
22
-
-
0037012136
-
Prothrombotic coagulation abnormalities preceding the hemolytic-uremic syndrome
-
Chandler WL, Jelacic S, Boster DR, et al. Prothrombotic coagulation abnormalities preceding the hemolytic-uremic syndrome. N Engl J Med 2002;346:23-32
-
(2002)
N Engl J Med
, vol.346
, pp. 23-32
-
-
Chandler, W.L.1
Jelacic, S.2
Boster, D.R.3
-
23
-
-
0026801584
-
Role of plasminogen-activator inhibitor type 1 in the pathogenesis and outcome of the hemolytic uremic syndrome
-
Bergstein JM, Riley M, Bang NU. Role of plasminogen-activator inhibitor type 1 in the pathogenesis and outcome of the hemolytic uremic syndrome. N Engl J Med 1992;327: 755-759
-
(1992)
N Engl J Med
, vol.327
, pp. 755-759
-
-
Bergstein, J.M.1
Riley, M.2
Bang, N.U.3
-
24
-
-
0034820680
-
Pathogenesis of Shiga toxin-induced hemolytic uremic syndrome
-
Ray PE, Liu XH. Pathogenesis of Shiga toxin-induced hemolytic uremic syndrome. Pediatr Nephrol 2001;16:823-839
-
(2001)
Pediatr Nephrol
, vol.16
, pp. 823-839
-
-
Ray, P.E.1
Liu, X.H.2
-
25
-
-
15244348050
-
Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
-
Tarr PI, Gordon CA, Chandler WL. Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome. Lancet 2005;365:1073-1086
-
(2005)
Lancet
, vol.365
, pp. 1073-1086
-
-
Tarr, P.I.1
Gordon, C.A.2
Chandler, W.L.3
-
26
-
-
0032528349
-
Shiga toxin type 1 activates tumor necrosis factor-alpha gene transcription and nuclear translocation of the transcriptional activators nuclear factor-kappa B and activator protein-1
-
Sakiri R, Ramegowda B, Tesh VL. Shiga toxin type 1 activates tumor necrosis factor-alpha gene transcription and nuclear translocation of the transcriptional activators nuclear factor-kappa B and activator protein-1. Blood 1998;92:558-566
-
(1998)
Blood
, vol.92
, pp. 558-566
-
-
Sakiri, R.1
Ramegowda, B.2
Tesh, V.L.3
-
27
-
-
23044459579
-
Shiga toxin enhances functional tissue factor on human glomerular endothelial cells: Implications for the pathophysiology of hemolytic uremic syndrome
-
Nestoridi E, Tsukurov O, Kushak RI, Ingelfinger JR, Grabowski EF. Shiga toxin enhances functional tissue factor on human glomerular endothelial cells: implications for the pathophysiology of hemolytic uremic syndrome. J Thromb Haemost 2005;3:752-762
-
(2005)
J Thromb Haemost
, vol.3
, pp. 752-762
-
-
Nestoridi, E.1
Tsukurov, O.2
Kushak, R.I.3
Ingelfinger, J.R.4
Grabowski, E.F.5
-
28
-
-
0030002051
-
Differentiation-associated toxin receptor modulation, cytokine production, and sensitivity to Shiga-like toxins in human monocytes and monocytic cell lines
-
Ramegowda B, Tesh VL. Differentiation-associated toxin receptor modulation, cytokine production, and sensitivity to Shiga-like toxins in human monocytes and monocytic cell lines. Infect Immun 1996;64:1173-1180
-
(1996)
Infect Immun
, vol.64
, pp. 1173-1180
-
-
Ramegowda, B.1
Tesh, V.L.2
-
29
-
-
0034080984
-
Cytotoxic effect of Shiga toxin-1 on human glomerular epithelial cells
-
Hughes AK, Stricklett PK, Schmid D, Kohan DE. Cytotoxic effect of Shiga toxin-1 on human glomerular epithelial cells. Kidney Int 2000;57:2350-2359
-
(2000)
Kidney Int
, vol.57
, pp. 2350-2359
-
-
Hughes, A.K.1
Stricklett, P.K.2
Schmid, D.3
Kohan, D.E.4
-
30
-
-
0024391413
-
Cancer-associated hemolytic-uremic syndrome: Analysis of 85 cases from a national registry
-
Lesesne JB, Rothschild N, Erickson B, et al. Cancer-associated hemolytic-uremic syndrome: analysis of 85 cases from a national registry. J Clin Oncol 1989;7:781-789
-
(1989)
J Clin Oncol
, vol.7
, pp. 781-789
-
-
Lesesne, J.B.1
Rothschild, N.2
Erickson, B.3
-
31
-
-
2942750005
-
Drug-induced thrombotic thrombocytopenic purpura/ hemolytic uremic syndrome: A concise review
-
Dlott JS, Danielson CF, Blue-Hnidy DE, McCarthy LJ. Drug-induced thrombotic thrombocytopenic purpura/ hemolytic uremic syndrome: a concise review. Ther Apher Dial 2004;8:102-111
-
(2004)
Ther Apher Dial
, vol.8
, pp. 102-111
-
-
Dlott, J.S.1
Danielson, C.F.2
Blue-Hnidy, D.E.3
McCarthy, L.J.4
-
33
-
-
0031941881
-
Hemolytic uremic syndrome associated with invasive Streptococcus pneumoniae infection
-
Cabrera GR, Fortenberry JD, Warshaw BL, et al. Hemolytic uremic syndrome associated with invasive Streptococcus pneumoniae infection. Pediatrics 1998;101:699-703
-
(1998)
Pediatrics
, vol.101
, pp. 699-703
-
-
Cabrera, G.R.1
Fortenberry, J.D.2
Warshaw, B.L.3
-
34
-
-
0017773222
-
Thomsen-Friedenreich antigen in haemolytic-uraemic syndrome
-
Klein PJ, Bulla M, Newman RA, et al. Thomsen-Friedenreich antigen in haemolytic-uraemic syndrome. Lancet 1977;2:1024-1025
-
(1977)
Lancet
, vol.2
, pp. 1024-1025
-
-
Klein, P.J.1
Bulla, M.2
Newman, R.A.3
-
36
-
-
0031913526
-
Pneumococcal meningitis complicated with hemolytic uremic syndrome: Report of two cases
-
Huang FY, Lin DS. Pneumococcal meningitis complicated with hemolytic uremic syndrome: report of two cases. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1998;39:58-61
-
(1998)
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi
, vol.39
, pp. 58-61
-
-
Huang, F.Y.1
Lin, D.S.2
-
37
-
-
0032950690
-
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Role of factor H abnormalities
-
Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.
-
Noris M, Ruggenenti P, Perna A, et al. Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura. J Am Soc Nephrol 1999;10: 281-293
-
(1999)
J Am Soc Nephrol
, vol.10
, pp. 281-293
-
-
Noris, M.1
Ruggenenti, P.2
Perna, A.3
-
38
-
-
0042329931
-
Haemolytic uraemic syndrome and mutations of the factor H gene: A registry-based study of German speaking countries
-
Neumann HP, Salzmann M, Bohnert-Iwan B, et al. Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries. J Med Genet 2003;40:676-681
-
(2003)
J Med Genet
, vol.40
, pp. 676-681
-
-
Neumann, H.P.1
Salzmann, M.2
Bohnert-Iwan, B.3
-
39
-
-
0031970553
-
Genetic studies into inherited and sporadic hemolytic uremic syndrome
-
Warwicker P, Goodship TH, Donne RL, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int 1998;53:836-844
-
(1998)
Kidney Int
, vol.53
, pp. 836-844
-
-
Warwicker, P.1
Goodship, T.H.2
Donne, R.L.3
-
40
-
-
0035128326
-
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition
-
Richards A, Buddies MR, Donne RL, et al. Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition. Am J Hum Genet 2001;68:485-490
-
(2001)
Am J Hum Genet
, vol.68
, pp. 485-490
-
-
Richards, A.1
Buddies, M.R.2
Donne, R.L.3
-
41
-
-
0035143299
-
The molecular basis of familial hemolytic uremic syndrome: Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
-
Caprioli J, Bettinaglio P, Zipfel PF, et al. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am Soc Nephrol 2001;12:297-307
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 297-307
-
-
Caprioli, J.1
Bettinaglio, P.2
Zipfel, P.F.3
-
42
-
-
1542318912
-
Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membrano-proliferative glomerulonephritis: Report and genetic analysis of 16 cases
-
Dragon-Durey MA, Fremeaux-Bacchi V, Loirat C, et al. Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membrano-proliferative glomerulonephritis: report and genetic analysis of 16 cases. J Am Soc Nephrol 2004;15:787-795
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 787-795
-
-
Dragon-Durey, M.A.1
Fremeaux-Bacchi, V.2
Loirat, C.3
-
43
-
-
27744452766
-
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
-
Kavanagh D, Kemp EJ, Mayland E, et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005;16: 2150-2155
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2150-2155
-
-
Kavanagh, D.1
Kemp, E.J.2
Mayland, E.3
-
44
-
-
0242570482
-
Familial haemolytic uraemic syndrome and an MCP mutation
-
Noris M, Brioschi S, Caprioli J, et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 2003; 362:1542-1547
-
(2003)
Lancet
, vol.362
, pp. 1542-1547
-
-
Noris, M.1
Brioschi, S.2
Caprioli, J.3
-
45
-
-
0242331610
-
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
-
Richards A, Kemp EJ, Liszewski MK, et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci USA 2003;100: 12966-12971
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 12966-12971
-
-
Richards, A.1
Kemp, E.J.2
Liszewski, M.K.3
-
46
-
-
20544437666
-
Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome
-
Dragon-Durey MA, Loirat C, Cloarec S, et al. Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005;16:555-563
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 555-563
-
-
Dragon-Durey, M.A.1
Loirat, C.2
Cloarec, S.3
-
47
-
-
0036881528
-
Thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome
-
Moake JL. Thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome. Arch Pathol Lab Med 2002; 126:1430-1433
-
(2002)
Arch Pathol Lab Med
, vol.126
, pp. 1430-1433
-
-
Moake, J.L.1
-
49
-
-
0036683408
-
Von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome
-
Remuzzi G, Galbusera M, Noris M, et al. von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Blood 2002;100:778-785
-
(2002)
Blood
, vol.100
, pp. 778-785
-
-
Remuzzi, G.1
Galbusera, M.2
Noris, M.3
-
50
-
-
0037339175
-
Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome
-
Veyradier A, Obert B, Haddad E, et al. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. J Pediatr 2003;142: 310-317
-
(2003)
J Pediatr
, vol.142
, pp. 310-317
-
-
Veyradier, A.1
Obert, B.2
Haddad, E.3
-
51
-
-
0031930634
-
A review of acute renal failure in children: Incidence, etiology and outcome
-
Moghal NE, Brocklebank JT, Meadow SR. A review of acute renal failure in children: incidence, etiology and outcome. Clin Nephrol 1998;49:91-95
-
(1998)
Clin Nephrol
, vol.49
, pp. 91-95
-
-
Moghal, N.E.1
Brocklebank, J.T.2
Meadow, S.R.3
-
52
-
-
0032755791
-
Enterohemorrhagic Escherichia coli (EHEC) in pediatric hemolytic-uremic syndrome: A prospective study in Germany and Austria
-
Verweyen HM, Karch H, Allerberger F, Zimmerhackl LB. Enterohemorrhagic Escherichia coli (EHEC) in pediatric hemolytic-uremic syndrome: a prospective study in Germany and Austria. Infection 1999;27:341-347
-
(1999)
Infection
, vol.27
, pp. 341-347
-
-
Verweyen, H.M.1
Karch, H.2
Allerberger, F.3
Zimmerhackl, L.B.4
-
53
-
-
0028172823
-
Escherichia coli O 157:H7-associated hemolytic-uremic syndrome after ingestion of contaminated hamburgers
-
Brandt JR, Fouser LS, Watkins SL, et al. Escherichia coli O 157:H7-associated hemolytic-uremic syndrome after ingestion of contaminated hamburgers. J Pediatr 1994;125: 519-526
-
(1994)
J Pediatr
, vol.125
, pp. 519-526
-
-
Brandt, J.R.1
Fouser, L.S.2
Watkins, S.L.3
-
54
-
-
0029821432
-
Hemolytic-uremic syndrome in a six-year-old girl after a urinary tract infection with Shiga-toxin-producing Escherichia coli O103:H2
-
Tarr PI, Fouser LS, Stapleton AE, et al. Hemolytic-uremic syndrome in a six-year-old girl after a urinary tract infection with Shiga-toxin-producing Escherichia coli O103:H2. N Engl J Med 1996;335:635-638
-
(1996)
N Engl J Med
, vol.335
, pp. 635-638
-
-
Tarr, P.I.1
Fouser, L.S.2
Stapleton, A.E.3
-
55
-
-
2442517486
-
Incidence of thrombotic thrombocytopenic purpura/hemolytic uremic syndrome
-
Miller DP, Kaye JA, Shea K, et al. Incidence of thrombotic thrombocytopenic purpura/hemolytic uremic syndrome. Epidemiology 2004;15:208-215
-
(2004)
Epidemiology
, vol.15
, pp. 208-215
-
-
Miller, D.P.1
Kaye, J.A.2
Shea, K.3
-
56
-
-
16244395474
-
Epidemiology of Escherichia coli O157:H7 outbreaks, United States, 1982-2002
-
Rangel JM, Sparling PH, Crowe C, Griffin PM, Swerdlow DL. Epidemiology of Escherichia coli O157:H7 outbreaks, United States, 1982-2002. Emerg Infect Dis 2005;11: 603-609
-
(2005)
Emerg Infect Dis
, vol.11
, pp. 603-609
-
-
Rangel, J.M.1
Sparling, P.H.2
Crowe, C.3
Griffin, P.M.4
Swerdlow, D.L.5
-
57
-
-
0034729744
-
The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli O157-.H7 infections
-
Wong CS, Jelacic S, Habeeb RL, Watkins SL, Tarr PI. The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli O157-.H7 infections. N Engl J Med 2000;342:1930-1936
-
(2000)
N Engl J Med
, vol.342
, pp. 1930-1936
-
-
Wong, C.S.1
Jelacic, S.2
Habeeb, R.L.3
Watkins, S.L.4
Tarr, P.I.5
-
58
-
-
0031175179
-
Predictors of hemolytic uremic syndrome in children during a large outbreak of Escherichia coli O157:H7 infections
-
Bell BP, Griffin PM, Lozano P, et al. Predictors of hemolytic uremic syndrome in children during a large outbreak of Escherichia coli O157:H7 infections. Pediatrics 1997;100:E12
-
(1997)
Pediatrics
, vol.100
-
-
Bell, B.P.1
Griffin, P.M.2
Lozano, P.3
-
59
-
-
0029093523
-
Incomplete hemolytic-uremic syndrome in Argentinean children with bloody diarrhea
-
Lopez EL, Contrini MM, Devoto S, et al. Incomplete hemolytic-uremic syndrome in Argentinean children with bloody diarrhea. J Pediatr 1995;127:364-367
-
(1995)
J Pediatr
, vol.127
, pp. 364-367
-
-
Lopez, E.L.1
Contrini, M.M.2
Devoto, S.3
-
60
-
-
0036331717
-
Invasive pneumococcal disease and hemolytic uremic syndrome
-
Brandt J, Wong C, Mihm S, et al. Invasive pneumococcal disease and hemolytic uremic syndrome. Pediatrics 2002; 110:371-376
-
(2002)
Pediatrics
, vol.110
, pp. 371-376
-
-
Brandt, J.1
Wong, C.2
Mihm, S.3
-
61
-
-
0031946665
-
Cholelithiasis following Escherichia coli Ol57:H7-associated hemolytic uremic syndrome
-
Brandt JR, Joseph MW, Fouser LS, et al. Cholelithiasis following Escherichia coli Ol57:H7-associated hemolytic uremic syndrome. Pediatr Nephrol 1998;12:222-225
-
(1998)
Pediatr Nephrol
, vol.12
, pp. 222-225
-
-
Brandt, J.R.1
Joseph, M.W.2
Fouser, L.S.3
-
62
-
-
2542420109
-
Non-enteropathic hemolytic uremic syndrome: Causes and short-term course
-
Constantinescu AR, Bitzan M, Weiss LS, et al. Non-enteropathic hemolytic uremic syndrome: causes and short-term course. Am J Kidney Dis 2004;43:976-982
-
(2004)
Am J Kidney Dis
, vol.43
, pp. 976-982
-
-
Constantinescu, A.R.1
Bitzan, M.2
Weiss, L.S.3
-
63
-
-
0028130110
-
Spectrum of extrarenal involvement in postdiarrheal hemolytic-uremic syndrome
-
Siegler RL. Spectrum of extrarenal involvement in postdiarrheal hemolytic-uremic syndrome. J Pediatr 1994;125:511-518
-
(1994)
J Pediatr
, vol.125
, pp. 511-518
-
-
Siegler, R.L.1
-
64
-
-
0020701017
-
Haemolytic-uraemic syndrome: An analysis of prognostic features
-
Trompeter RS, Schwartz R, Chantier C, et al. Haemolytic-uraemic syndrome: an analysis of prognostic features. Arch Dis Child 1983;58:101-105
-
(1983)
Arch Dis Child
, vol.58
, pp. 101-105
-
-
Trompeter, R.S.1
Schwartz, R.2
Chantier, C.3
-
65
-
-
0029958884
-
Atypical hemolytic-uremic syndrome: A comparison with postdiarrheal disease
-
Siegler RL, Pavia AT, Hansen FL, Christofferson RD, Cook JB. Atypical hemolytic-uremic syndrome: a comparison with postdiarrheal disease. J Pediatr 1996;128:505-511
-
(1996)
J Pediatr
, vol.128
, pp. 505-511
-
-
Siegler, R.L.1
Pavia, A.T.2
Hansen, F.L.3
Christofferson, R.D.4
Cook, J.B.5
-
66
-
-
0026555581
-
Response to plasma exchange and splenectomy in thrombotic thrombocytopenic purpura. A 10-year experience at a single institution
-
Onundarson PT, Rowe JM, Heal JM, Francis CW. Response to plasma exchange and splenectomy in thrombotic thrombocytopenic purpura. A 10-year experience at a single institution. Arch Intern Med 1992;152:791-796
-
(1992)
Arch Intern Med
, vol.152
, pp. 791-796
-
-
Onundarson, P.T.1
Rowe, J.M.2
Heal, J.M.3
Francis, C.W.4
-
67
-
-
0035008965
-
Sorbitol-fermenting Shiga toxin-producing Escherichia coli O157:H(-) strains: Epidemiology, phenotypic and molecular characteristics, and microbiological diagnosis
-
Karch H, Bielaszewska M. Sorbitol-fermenting Shiga toxin-producing Escherichia coli O157:H(-) strains: epidemiology, phenotypic and molecular characteristics, and microbiological diagnosis. J Clin Microbiol 2001;39:2043-2049
-
(2001)
J Clin Microbiol
, vol.39
, pp. 2043-2049
-
-
Karch, H.1
Bielaszewska, M.2
-
69
-
-
0002911516
-
Disorders of propionate and methylmalonate metabolism
-
Scriver C, Baudet A, Sly W, Valle D, eds. New York: McGraw-Hill
-
Fenton W, Rosenberg L. Disorders of propionate and methylmalonate metabolism. In: Scriver C, Baudet A, Sly W, Valle D, eds. Metaboloic and Molecular Basis of Inherited Disease. New York: McGraw-Hill; 2001:2165-2193
-
(2001)
Metaboloic and Molecular Basis of Inherited Disease
, pp. 2165-2193
-
-
Fenton, W.1
Rosenberg, L.2
-
70
-
-
27744564894
-
Relative nephroprotection during Escherichia coli O157:H7 infections: Association with intravenous volume expansion
-
Ake JA, Jelacic S, Ciol MA, et al. Relative nephroprotection during Escherichia coli O157:H7 infections: association with intravenous volume expansion. Pediatrics 2005;115:e673-e680
-
(2005)
Pediatrics
, vol.115
-
-
Ake, J.A.1
Jelacic, S.2
Ciol, M.A.3
-
71
-
-
18244407993
-
Phase 1 safety and pharmacokinetic study of chimeric murine-human monoclonal antibody c alpha Stx2 administered intravenously to healthy adult volunteers
-
Dowling TC, Chavailkz PA, Young DG, et al. Phase 1 safety and pharmacokinetic study of chimeric murine-human monoclonal antibody c alpha Stx2 administered intravenously to healthy adult volunteers. Antimicrob Agents Chemother 2005;49:1808-1812
-
(2005)
Antimicrob Agents Chemother
, vol.49
, pp. 1808-1812
-
-
Dowling, T.C.1
Chavailkz, P.A.2
Young, D.G.3
-
72
-
-
1142297326
-
Prospects for preventing serious systemic toxemic complications of Shiga toxin-producing Escherichia coli infections using Shiga toxin receptor analogues
-
Karmali MA. Prospects for preventing serious systemic toxemic complications of Shiga toxin-producing Escherichia coli infections using Shiga toxin receptor analogues. J Infect Dis 2004;189:355-359
-
(2004)
J Infect Dis
, vol.189
, pp. 355-359
-
-
Karmali, M.A.1
-
73
-
-
0028034212
-
A multistate outbreak of Escherichia coli O157:H7-associated bloody diarrhea and hemolytic uremic syndrome from hamburgers. The Washington experience
-
Bell BP, Goldoft M, Griffin PM, et al. A multistate outbreak of Escherichia coli O157:H7-associated bloody diarrhea and hemolytic uremic syndrome from hamburgers. The Washington experience. JAMA 1994;272:1349-1353
-
(1994)
JAMA
, vol.272
, pp. 1349-1353
-
-
Bell, B.P.1
Goldoft, M.2
Griffin, P.M.3
-
74
-
-
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, Meinen 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;45:415-421
-
(2005)
Am J Kidney Dis
, vol.45
, pp. 415-421
-
-
Licht, C.1
Weyersberg, A.2
Meinen, S.3
-
75
-
-
0034957282
-
Successful plasma therapy in hemolytic uremic syndrome with factor H deficiency
-
Nathanson S, Fremeaux-Bacchi V, Deschenes G. Successful plasma therapy in hemolytic uremic syndrome with factor H deficiency. Pediatr Nephrol 2001;16:554-556
-
(2001)
Pediatr Nephrol
, vol.16
, pp. 554-556
-
-
Nathanson, S.1
Fremeaux-Bacchi, V.2
Deschenes, G.3
-
76
-
-
0242694369
-
The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children
-
Loirat C, Niaudet P. The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children. Pediatr Nephrol 2003;18:1095-1101
-
(2003)
Pediatr Nephrol
, vol.18
, pp. 1095-1101
-
-
Loirat, C.1
Niaudet, P.2
-
77
-
-
0032571989
-
Recurrence of hemolytic-uremic syndrome in renal transplant recipients: A meta-analysis
-
Ducloux D, Rebibou JM, Semhoun-Ducloux S, et al. Recurrence of hemolytic-uremic syndrome in renal transplant recipients: a meta-analysis. Transplantation 1998;65: 1405-1407
-
(1998)
Transplantation
, vol.65
, pp. 1405-1407
-
-
Ducloux, D.1
Rebibou, J.M.2
Semhoun-Ducloux, S.3
-
78
-
-
0035959420
-
Recurrence of hemolytic uremic syndrome after renal transplantation in children: A report of the North American Pediatric Renal Transplant Cooperative Study
-
Quan A, Sullivan EK, Alexander SR. Recurrence of hemolytic uremic syndrome after renal transplantation in children: a report of the North American Pediatric Renal Transplant Cooperative Study. Transplantation 2001;72: 742-745
-
(2001)
Transplantation
, vol.72
, pp. 742-745
-
-
Quan, A.1
Sullivan, E.K.2
Alexander, S.R.3
-
79
-
-
1842637606
-
Attempted treatment of factor H deficiency by liver transplantation
-
Cheong HI, Lee BS, Kang HG, et al. Attempted treatment of factor H deficiency by liver transplantation. Pediatr Nephrol 2004;19:454-458
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 454-458
-
-
Cheong, H.I.1
Lee, B.S.2
Kang, H.G.3
-
80
-
-
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 NY Pathol Soc 1924;24:21-24
-
(1924)
Proc NY Pathol Soc
, vol.24
, pp. 21-24
-
-
Moschcowitz, E.1
-
81
-
-
0033358540
-
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene
-
Colige A, Sieron AL, Li SW, et al. Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene. Am J Hum Genet 1999;65:308-317
-
(1999)
Am J Hum Genet
, vol.65
, pp. 308-317
-
-
Colige, A.1
Sieron, A.L.2
Li, S.W.3
-
82
-
-
6344237724
-
ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome
-
Dagoneau N, Benoist-Lasselin C, Huber C, et al. ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome. Am J Hum Genet 2004;75:801-806
-
(2004)
Am J Hum Genet
, vol.75
, pp. 801-806
-
-
Dagoneau, N.1
Benoist-Lasselin, C.2
Huber, C.3
-
83
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy GG, Nichols WC, Lian EC, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001;413:488-494
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
-
84
-
-
72849154313
-
Studies on thrombopoiesis, I: A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency
-
Schulman I, Pierce M, Lukens A, Currimbhoy Z. Studies on thrombopoiesis, I: a factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency. Blood 1960;16:943-957
-
(1960)
Blood
, vol.16
, pp. 943-957
-
-
Schulman, I.1
Pierce, M.2
Lukens, A.3
Currimbhoy, Z.4
-
85
-
-
0018098453
-
Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia
-
Upshaw JD Jr. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. N Engl J Med 1978;298:1350-1352
-
(1978)
N Engl J Med
, vol.298
, pp. 1350-1352
-
-
Upshaw Jr., J.D.1
-
86
-
-
0037372508
-
Von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP
-
Schneppenheim R, Budde U, Oyen F, et al. von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Blood 2003;101:1845-1850
-
(2003)
Blood
, vol.101
, pp. 1845-1850
-
-
Schneppenheim, R.1
Budde, U.2
Oyen, F.3
-
87
-
-
0037226460
-
Thrombotic thrombocytopenic purpura in a newborn
-
Jubinsky PT, Moraille R, Tsai HM. Thrombotic thrombocytopenic purpura in a newborn. J Perinatol 2003;23:85-87
-
(2003)
J Perinatol
, vol.23
, pp. 85-87
-
-
Jubinsky, P.T.1
Moraille, R.2
Tsai, H.M.3
-
88
-
-
0035408661
-
Upshaw-Schulman syndrome revisited: A concept of congenital thrombotic thrombocytopenic purpura
-
Kinoshita S, Yoshioka A, Park YD, et al. Upshaw-Schulman syndrome revisited: a concept of congenital thrombotic thrombocytopenic purpura. Int J Hematol 2001;74:101-108
-
(2001)
Int J Hematol
, vol.74
, pp. 101-108
-
-
Kinoshita, S.1
Yoshioka, A.2
Park, Y.D.3
-
89
-
-
0026527356
-
Chronic relapsing thrombotic thrombocytopenic purpura in infants with large von Willebrand factor multimers during remission
-
Chintagumpala MM, Hurwitz RL, Moake JL, Mahoney DH, Steuber CP. Chronic relapsing thrombotic thrombocytopenic purpura in infants with large von Willebrand factor multimers during remission. J Pediatr 1992;120:49-53
-
(1992)
J Pediatr
, vol.120
, pp. 49-53
-
-
Chintagumpala, M.M.1
Hurwitz, R.L.2
Moake, J.L.3
Mahoney, D.H.4
Steuber, C.P.5
-
90
-
-
10744226155
-
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome
-
Matsumoto M, Kokame K, Soejima K, et al. Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome. Blood 2004;103:1305-1310
-
(2004)
Blood
, vol.103
, pp. 1305-1310
-
-
Matsumoto, M.1
Kokame, K.2
Soejima, K.3
-
91
-
-
3843152878
-
Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency
-
Schiff DE, Roberts WD, Willert J, Tsai HM. Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency. J Pediatr Hematol Oncol 2004;26:535-538
-
(2004)
J Pediatr Hematol Oncol
, vol.26
, pp. 535-538
-
-
Schiff, D.E.1
Roberts, W.D.2
Willert, J.3
Tsai, H.M.4
-
93
-
-
0023926689
-
Thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome in three siblings
-
Elias M, Horowitz J, Tal I, Kohn D, Flatau E. Thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome in three siblings. Arch Dis Child 1988;63:644-646
-
(1988)
Arch Dis Child
, vol.63
, pp. 644-646
-
-
Elias, M.1
Horowitz, J.2
Tal, I.3
Kohn, D.4
Flatau, E.5
-
94
-
-
1642474420
-
Ventricular tachycardia as a presenting symptom in a child with thrombotic thrombocytopenic purpura
-
Buyukavci M, Olgun H, Kertmen B, Tan H, Ceviz N. Ventricular tachycardia as a presenting symptom in a child with thrombotic thrombocytopenic purpura. Thromb Haemost 2004;91:198-200
-
(2004)
Thromb Haemost
, vol.91
, pp. 198-200
-
-
Buyukavci, M.1
Olgun, H.2
Kertmen, B.3
Tan, H.4
Ceviz, N.5
-
95
-
-
0034490066
-
Von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura
-
Allford SL, Harrison P, Lawrie AS, et al. Von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura. Br J Haematol 2000;111:1215-1222
-
(2000)
Br J Haematol
, vol.111
, pp. 1215-1222
-
-
Allford, S.L.1
Harrison, P.2
Lawrie, A.S.3
-
96
-
-
0034994133
-
Ten years of prophylactic treatment with fresh-frozen plasma in a child with chronic relapsing thrombotic thrombocytopenic purpura as a result of a congenital deficiency of von Willebrand factor-cleaving protease
-
Barbot J, Costa E, Guerra M, et al. Ten years of prophylactic treatment with fresh-frozen plasma in a child with chronic relapsing thrombotic thrombocytopenic purpura as a result of a congenital deficiency of von Willebrand factor-cleaving protease. Br J Haematol 2001;113:649-651
-
(2001)
Br J Haematol
, vol.113
, pp. 649-651
-
-
Barbot, J.1
Costa, E.2
Guerra, M.3
-
97
-
-
0012580388
-
ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity
-
Savasan S, Lee SK, Ginsburg D, Tsai HM. ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity. Blood 2003;101:4449-4451
-
(2003)
Blood
, vol.101
, pp. 4449-4451
-
-
Savasan, S.1
Lee, S.K.2
Ginsburg, D.3
Tsai, H.M.4
-
98
-
-
0032841681
-
New strategies in diagnosis and treatment of thrombotic thrombocytopenic purpura: Case report and review
-
Haberle J, Kehrel B, Ritter J, et al. New strategies in diagnosis and treatment of thrombotic thrombocytopenic purpura: case report and review. Eur J Pediatr 1999;158: 883-887
-
(1999)
Eur J Pediatr
, vol.158
, pp. 883-887
-
-
Haberle, J.1
Kehrel, B.2
Ritter, J.3
-
99
-
-
0031925404
-
Cellular source of serum lactate dehydrogenase elevation in patients with thrombotic thrombocytopenic purpura
-
Cohen JA, Brecher ME, Bandarenko N. Cellular source of serum lactate dehydrogenase elevation in patients with thrombotic thrombocytopenic purpura. J Clin Apher 1998; 13:16-19
-
(1998)
J Clin Apher
, vol.13
, pp. 16-19
-
-
Cohen, J.A.1
Brecher, M.E.2
Bandarenko, N.3
-
100
-
-
0032569884
-
Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
-
Furlan M, Rubles R, Galbusera M, et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med 1998;339:1578-1584
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Rubles, R.2
Galbusera, M.3
-
101
-
-
0030973267
-
Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
-
Furlan M, Rubles R, Solenthaler M, et al. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood 1997;89:3097-3103
-
(1997)
Blood
, vol.89
, pp. 3097-3103
-
-
Furlan, M.1
Rubles, R.2
Solenthaler, M.3
-
102
-
-
0024395146
-
Enhanced proteolysis of plasma von Willebrand factor in thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome
-
Mannucci PM, Lombardi R, Lattuada A, et al. Enhanced proteolysis of plasma von Willebrand factor in thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome. Blood 1989;74:978-983
-
(1989)
Blood
, vol.74
, pp. 978-983
-
-
Mannucci, P.M.1
Lombardi, R.2
Lattuada, A.3
-
103
-
-
0020428664
-
Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura
-
Moake JL, Rudy CK, Troll JH, et al. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 1982;307:1432-1435
-
(1982)
N Engl J Med
, vol.307
, pp. 1432-1435
-
-
Moake, J.L.1
Rudy, C.K.2
Troll, J.H.3
-
104
-
-
0033168804
-
Von Willebrand factor propeptide in vascular disorders: A tool to distinguish between acute and chronic endothelial cell perturbation
-
van Mourik JA, Boertjes R, Huisveld IA, et al. von Willebrand factor propeptide in vascular disorders: A tool to distinguish between acute and chronic endothelial cell perturbation. Blood 1999;94:179-185
-
(1999)
Blood
, vol.94
, pp. 179-185
-
-
Van Mourik, J.A.1
Boertjes, R.2
Huisveld, I.A.3
-
105
-
-
0034847605
-
Congenital microangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease
-
Savasan S, Taub JW, Buck S, et al. Congenital microangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease. J Pediatr Hematol Oncol 2001;23:364-367
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 364-367
-
-
Savasan, S.1
Taub, J.W.2
Buck, S.3
-
106
-
-
0024336513
-
Relationship between human development and disappearance of unusually large von Willebrand factor multimers from plasma
-
Katz JA, Moake JL, McPherson PD, et al. Relationship between human development and disappearance of unusually large von Willebrand factor multimers from plasma. Blood 1989;73:1851-1858
-
(1989)
Blood
, vol.73
, pp. 1851-1858
-
-
Katz, J.A.1
Moake, J.L.2
McPherson, P.D.3
-
107
-
-
0036877354
-
Ultralarge von Willebrand factor multimers and normal ADAMTS13 activity in the umbilical cord blood
-
Tsai HM, Sarode R, Dowries KA. Ultralarge von Willebrand factor multimers and normal ADAMTS13 activity in the umbilical cord blood. Thromb Res 2002;108:121-125
-
(2002)
Thromb Res
, vol.108
, pp. 121-125
-
-
Tsai, H.M.1
Sarode, R.2
Dowries, K.A.3
-
108
-
-
0024591755
-
Fetal and neonatal von Willebrand factor (vWF) is unusually large and similar to the vWF in patients with thrombotic thrombocytopenic purpura
-
Weinstein MJ, Blanchard R, Moake JL, Vosburgh E, Moise K. Fetal and neonatal von Willebrand factor (vWF) is unusually large and similar to the vWF in patients with thrombotic thrombocytopenic purpura. Br J Haematol 1989;72:68-72
-
(1989)
Br J Haematol
, vol.72
, pp. 68-72
-
-
Weinstein, M.J.1
Blanchard, R.2
Moake, J.L.3
Vosburgh, E.4
Moise, K.5
-
109
-
-
14844296516
-
VWF-deaving protease (ADAMTS13) in premature infants
-
Hellstrom-Westas L, Ley D, Berg AC, Kristoffersson AC, Holmberg L. VWF-deaving protease (ADAMTS13) in premature infants. Acta Paediatr 2005;94:205-210
-
(2005)
Acta Paediatr
, vol.94
, pp. 205-210
-
-
Hellstrom-Westas, L.1
Ley, D.2
Berg, A.C.3
Kristoffersson, A.C.4
Holmberg, L.5
-
110
-
-
0036785033
-
Plasma levels of the von Willebrand factor-cleaving protease in physiological and pathological conditions in children
-
Kavakli K, Canciani MT, Mannucci PM. Plasma levels of the von Willebrand factor-cleaving protease in physiological and pathological conditions in children. Pediatr Hematol Oncol 2002;19:467-473
-
(2002)
Pediatr Hematol Oncol
, vol.19
, pp. 467-473
-
-
Kavakli, K.1
Canciani, M.T.2
Mannucci, P.M.3
-
111
-
-
0035525768
-
Changes in health and disease of the metalloprotease that cleaves von Willebrand factor
-
Mannucci PM, Canciani MT, Forza I, et al. Changes in health and disease of the metalloprotease that cleaves von Willebrand factor. Blood 2001;98:2730-2735
-
(2001)
Blood
, vol.98
, pp. 2730-2735
-
-
Mannucci, P.M.1
Canciani, M.T.2
Forza, I.3
-
112
-
-
4644327577
-
The activity of the von Willebrand factor cleaving protease ADAMTS-13 in newborn infants
-
Schmugge M, Dunn MS, Amankwah KS, et al. The activity of the von Willebrand factor cleaving protease ADAMTS-13 in newborn infants. J Thromb Haemost 2004;2:228-233
-
(2004)
J Thromb Haemost
, vol.2
, pp. 228-233
-
-
Schmugge, M.1
Dunn, M.S.2
Amankwah, K.S.3
-
113
-
-
0037513434
-
Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency
-
Assink K, Schiphorst R, Allford S, et al. Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency. Kidney Int 2003;63:1995-1999
-
(2003)
Kidney Int
, vol.63
, pp. 1995-1999
-
-
Assink, K.1
Schiphorst, R.2
Allford, S.3
-
114
-
-
0346095394
-
Genetic defects leading to hereditary thrombotic thrombocytopenic purpura
-
Kokame K, Miyata T. Genetic defects leading to hereditary thrombotic thrombocytopenic purpura. Semin Hematol 2004;41:34-40
-
(2004)
Semin Hematol
, vol.41
, pp. 34-40
-
-
Kokame, K.1
Miyata, T.2
-
116
-
-
0032918258
-
Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Morselli B, Sandoz P, Lämmle B. Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 1999;81:8-13
-
(1999)
Thromb Haemost
, vol.81
, pp. 8-13
-
-
Furlan, M.1
Robles, R.2
Morselli, B.3
Sandoz, P.4
Lämmle, B.5
-
117
-
-
0036399645
-
Remission of thrombotic thrombocytopenic purpura in a patient with compound heterozygous deficiency of von Willebrand factor-cleaving protease by infusion of solvent/detergent plasma
-
Kentouche K, Budde U, Furlan M, et al. Remission of thrombotic thrombocytopenic purpura in a patient with compound heterozygous deficiency of von Willebrand factor-cleaving protease by infusion of solvent/detergent plasma. Acta Paediatr 2002;91:1056-1059
-
(2002)
Acta Paediatr
, vol.91
, pp. 1056-1059
-
-
Kentouche, K.1
Budde, U.2
Furlan, M.3
-
118
-
-
0021959985
-
Effects of fresh-frozen plasma and its cryosupernatant fraction on von Willebrand factor multimeric forms in chronic relapsing thrombotic thrombocytopenic purpura
-
Moake JL, Byrnes JJ, Troll JH, et al. Effects of fresh-frozen plasma and its cryosupernatant fraction on von Willebrand factor multimeric forms in chronic relapsing thrombotic thrombocytopenic purpura. Blood 1985;65:1232-1236
-
(1985)
Blood
, vol.65
, pp. 1232-1236
-
-
Moake, J.L.1
Byrnes, J.J.2
Troll, J.H.3
-
119
-
-
0028233149
-
Solvent/detergent-treated plasma suppresses shear-induced platelet aggregation and prevents episodes of thrombotic thrombocytopenic purpura
-
Moake J, Chintagumpala M, Turner N, et al. Solvent/detergent-treated plasma suppresses shear-induced platelet aggregation and prevents episodes of thrombotic thrombocytopenic purpura. Blood 1994;84:490-497
-
(1994)
Blood
, vol.84
, pp. 490-497
-
-
Moake, J.1
Chintagumpala, M.2
Turner, N.3
-
120
-
-
0033497835
-
Close relationship between systemic lupus erythematosus and thrombotic thrombocytopenic purpura in childhood
-
Brunner HI, Freedman M, Silverman ED. Close relationship between systemic lupus erythematosus and thrombotic thrombocytopenic purpura in childhood. Arthritis Rheum 1999;42:2346-2355
-
(1999)
Arthritis Rheum
, vol.42
, pp. 2346-2355
-
-
Brunner, H.I.1
Freedman, M.2
Silverman, E.D.3
-
121
-
-
0141996978
-
Thrombotic thrombocytopenic purpura as a rare complication in childhood systemic lupus erythematosus: Case report and literature review
-
Chak WK, Lam DS, Lo WH, Hui CM, Wong SN. Thrombotic thrombocytopenic purpura as a rare complication in childhood systemic lupus erythematosus: case report and literature review. Hong Kong Med J 2003;9:363-368
-
(2003)
Hong Kong Med J
, vol.9
, pp. 363-368
-
-
Chak, W.K.1
Lam, D.S.2
Lo, W.H.3
Hui, C.M.4
Wong, S.N.5
-
122
-
-
0034861756
-
Acquired deficiency of von Willebrand factor-cleaving protease in a patient suffering from acute systemic lupus erythematosus
-
Gungor T, Furlan M, Lämmle B, Kuhn F, Seger RA. Acquired deficiency of von Willebrand factor-cleaving protease in a patient suffering from acute systemic lupus erythematosus. Rheumatology (Oxford) 2001;40: 940-942
-
(2001)
Rheumatology (Oxford)
, vol.40
, pp. 940-942
-
-
Gungor, T.1
Furlan, M.2
Lämmle, B.3
Kuhn, F.4
Seger, R.A.5
-
123
-
-
2542420893
-
Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins
-
Studt JD, Hovinga JA, Radonic R, et al. Familial acquired thrombotic thrombocytopenic purpura: ADAMTS13 inhibitory autoantibodies in identical twins. Blood 2004;103: 4195-4197
-
(2004)
Blood
, vol.103
, pp. 4195-4197
-
-
Studt, J.D.1
Hovinga, J.A.2
Radonic, R.3
-
124
-
-
10744228488
-
Post-transplantation thrombotic thrombocytopenic purpura: A single-center experience and a contemporary review
-
Elliott MA, Nichols WL Jr, Plumhoff EA, et al. Post-transplantation thrombotic thrombocytopenic purpura: a single-center experience and a contemporary review. Mayo Clin Proc 2003;78:421-430
-
(2003)
Mayo Clin Proc
, vol.78
, pp. 421-430
-
-
Elliott, M.A.1
Nichols Jr., W.L.2
Plumhoff, E.A.3
-
125
-
-
0035003931
-
The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation
-
Fuge R, Bird JM, Fraser A, et al. The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation. Br J Haematol 2001;113:58-64
-
(2001)
Br J Haematol
, vol.113
, pp. 58-64
-
-
Fuge, R.1
Bird, J.M.2
Fraser, A.3
-
126
-
-
18544363871
-
Thrombotic thrombocytopenic purpura after allogeneic stem cell transplantation: A survey of the European Group for Blood and Marrow Transplantation (EBMT)
-
Ruutu T, Hermans J, Niederwieser D, et al. Thrombotic thrombocytopenic purpura after allogeneic stem cell transplantation: a survey of the European Group for Blood and Marrow Transplantation (EBMT). Br J Haematol 2002; 118:1112-1119
-
(2002)
Br J Haematol
, vol.118
, pp. 1112-1119
-
-
Ruutu, T.1
Hermans, J.2
Niederwieser, D.3
-
127
-
-
0033757978
-
Impact of thrombotic thrombocytopenic purpura on leukemic children undergoing bone marrow transplantation
-
126a. Uderzo C, Funagalii M, DeLorenzo P, et al. Impact of thrombotic thrombocytopenic purpura on leukemic children undergoing bone marrow transplantation. Bone Marrow Transplant 2000;26:1005-1009
-
(2000)
Bone Marrow Transplant
, vol.26
, pp. 1005-1009
-
-
Uderzo, C.1
Funagalii, M.2
DeLorenzo, P.3
-
128
-
-
0034775082
-
Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy
-
Arai S, Allan C, Streiff M, et al. Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy. Hematol J 2001;2:292-299
-
(2001)
Hematol J
, vol.2
, pp. 292-299
-
-
Arai, S.1
Allan, C.2
Streiff, M.3
-
129
-
-
0033151555
-
Willebrand factor proteolysis is deficient in classic, but not in bone marrow transplantation-associated, thrombotic thrombocytopenic purpura
-
van der Plas RM, Schiphorst ME, Huizinga EG, et al. von Willebrand factor proteolysis is deficient in classic, but not in bone marrow transplantation-associated, thrombotic thrombocytopenic purpura. Blood 1999;93:3798-3802
-
(1999)
Blood
, vol.93
, pp. 3798-3802
-
-
Plas, R.M.1
Schiphorst, M.E.2
Huizinga, E.G.3
Von Al, E.4
-
130
-
-
0036893469
-
Successful treatment of a young infant who developed high-liter inhibitors against VWF-cleaving protease (ADAMTS-13): Important discrimination from Upshaw-Schulman syndrome
-
Ashida A, Nakamura H, Yoden A, et al. Successful treatment of a young infant who developed high-liter inhibitors against VWF-cleaving protease (ADAMTS-13): important discrimination from Upshaw-Schulman syndrome. Am J Hematol 2002;71:318-322
-
(2002)
Am J Hematol
, vol.71
, pp. 318-322
-
-
Ashida, A.1
Nakamura, H.2
Yoden, A.3
-
131
-
-
0037397410
-
Case series of thrombotic thrombocytopenic purpura in children and adolescents
-
Horton TM, Stone JD, Yee D, et al. Case series of thrombotic thrombocytopenic purpura in children and adolescents. J Pediatr Hematol Oncol 2003;25:336-339
-
(2003)
J Pediatr Hematol Oncol
, vol.25
, pp. 336-339
-
-
Horton, T.M.1
Stone, J.D.2
Yee, D.3
-
132
-
-
0036159297
-
Thrombotic thrombocytopenic purpura attributable to von Willebrand factor-cleaving protease inhibitor in an 8-year-old boy
-
Robson WL, Tsai HM. Thrombotic thrombocytopenic purpura attributable to von Willebrand factor-cleaving protease inhibitor in an 8-year-old boy. Pediatrics 2002; 109:322-325
-
(2002)
Pediatrics
, vol.109
, pp. 322-325
-
-
Robson, W.L.1
Tsai, H.M.2
-
133
-
-
0034972253
-
Willebrand factor-cleaving protease in childhood diarrhoea-associated haemolytic uraemic syndrome
-
Hunt BJ, Lämmle B, Nevard CH, Haycock GB, von Furlan M. Willebrand factor-cleaving protease in childhood diarrhoea-associated haemolytic uraemic syndrome. Thromb Haemost 2001;85:975-978
-
(2001)
Thromb Haemost
, vol.85
, pp. 975-978
-
-
Hunt, B.J.1
Lämmle, B.2
Nevard, C.H.3
Haycock, G.B.4
Von Furlan, M.5
-
134
-
-
0025081667
-
A study of plasma exchange in TTP
-
The Canadian Apheresis Study Group
-
Rock G, Shumak K, Nair R. A study of plasma exchange in TTP. The Canadian Apheresis Study Group. Prog Clin Biol Res 1990;337:125-127
-
(1990)
Prog Clin Biol Res
, vol.337
, pp. 125-127
-
-
Rock, G.1
Shumak, K.2
Nair, R.3
-
135
-
-
0025999820
-
Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients
-
Bell WR, Braine HG, Ness PM, Kickler TS. Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients. N Engl J Med 1991;325:398-403
-
(1991)
N Engl J Med
, vol.325
, pp. 398-403
-
-
Bell, W.R.1
Braine, H.G.2
Ness, P.M.3
Kickler, T.S.4
-
136
-
-
0034663327
-
How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
-
George JN. How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Blood 2000;96:1223-1229
-
(2000)
Blood
, vol.96
, pp. 1223-1229
-
-
George, J.N.1
-
137
-
-
0004900267
-
Improved survival with plasma exchange in patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
-
Lara PN Jr, Coe TL, Zhou H, et al. Improved survival with plasma exchange in patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Am J Med 1999;107:573-579
-
(1999)
Am J Med
, vol.107
, pp. 573-579
-
-
Lara Jr., P.N.1
Coe, T.L.2
Zhou, H.3
-
140
-
-
0037250139
-
High-dose plasma infusion versus plasma exchange as early treatment of thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome
-
Coppo P, Bussel A, Charrier S, et al. High-dose plasma infusion versus plasma exchange as early treatment of thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome. Medicine (Baltimore) 2003;82:27-38
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 27-38
-
-
Coppo, P.1
Bussel, A.2
Charrier, S.3
-
141
-
-
0031436280
-
Antiplatelet agents in thrombotic thrombocytopenic purpura (TTP). Results of a randomized multicenter trial by the Italian Cooperative Group for TTP
-
Bobbio-Pallavicini E, Gugliotta L, Centurioni R, et al. Antiplatelet agents in thrombotic thrombocytopenic purpura (TTP). Results of a randomized multicenter trial by the Italian Cooperative Group for TTP. Haematologica 1997; 82:429-435
-
(1997)
Haematologica
, vol.82
, pp. 429-435
-
-
Bobbio-Pallavicini, E.1
Gugliotta, L.2
Centurioni, R.3
-
142
-
-
0037883547
-
Use of vincristine and cyclosporine in childhood thrombotic thrombocytopenic purpura
-
Jayabose S, Levendoglu-Tugal O, Ozkayanak MF, et al. Use of vincristine and cyclosporine in childhood thrombotic thrombocytopenic purpura. J Pediatr Hematol Oncol 2003; 25:421-425
-
(2003)
J Pediatr Hematol Oncol
, vol.25
, pp. 421-425
-
-
Jayabose, S.1
Levendoglu-Tugal, O.2
Ozkayanak, M.F.3
-
143
-
-
0024986256
-
Rapid improvement of thrombotic thrombocytopenic purpura with vincristine and plasmapheresis
-
Welborn JL, Emrick P, Acevedo M. Rapid improvement of thrombotic thrombocytopenic purpura with vincristine and plasmapheresis. Am J Hematol 1990;35:18-21
-
(1990)
Am J Hematol
, vol.35
, pp. 18-21
-
-
Welborn, J.L.1
Emrick, P.2
Acevedo, M.3
-
144
-
-
0031840296
-
Successful use of cyclosporine a in the treatment of refractory thrombotic thrombocytopenic purpura
-
Hand JP, Lawlor ER, Yong CK, Davis JH. Successful use of cyclosporine A in the treatment of refractory thrombotic thrombocytopenic purpura. Br J Haematol 1998;100:597-599
-
(1998)
Br J Haematol
, vol.100
, pp. 597-599
-
-
Hand, J.P.1
Lawlor, E.R.2
Yong, C.K.3
Davis, J.H.4
-
145
-
-
0034124281
-
Effects of intravenous immunoglobulin in a patient with intermittent thrombotic thrombocytopenic purpura
-
Kondo H, Imamura T. Effects of intravenous immunoglobulin in a patient with intermittent thrombotic thrombocytopenic purpura. Br J Haematol 2000;108:880-882
-
(2000)
Br J Haematol
, vol.108
, pp. 880-882
-
-
Kondo, H.1
Imamura, T.2
-
146
-
-
17944371079
-
Efficacy of intravenous immunoglobulin in the treatment of thrombotic thrombocytopaenic purpura. A study of 44 cases
-
Dervenoulas J, Tsirigotis P, Bollas G, et al. Efficacy of intravenous immunoglobulin in the treatment of thrombotic thrombocytopaenic purpura. A study of 44 cases. Acta Haematol 2001;105:204-208
-
(2001)
Acta Haematol
, vol.105
, pp. 204-208
-
-
Dervenoulas, J.1
Tsirigotis, P.2
Bollas, G.3
-
147
-
-
11144342822
-
Rituximab for the treatment of refractory idiopathic thrombocytopenic purpura (ITP) and thrombotic thrombocytopenic purpura (TTP): Report of three cases
-
Koulova L, Alexandrescu D, Dutcher JP, et al. Rituximab for the treatment of refractory idiopathic thrombocytopenic purpura (ITP) and thrombotic thrombocytopenic purpura (TTP): report of three cases. Am J Hematol 2005;78: 49-54
-
(2005)
Am J Hematol
, vol.78
, pp. 49-54
-
-
Koulova, L.1
Alexandrescu, D.2
Dutcher, J.P.3
-
148
-
-
24744472059
-
Efficiency of curative and prophylactic treatment with rituximab in ADAMTS13 deficient-thrombotic thrombocytopenic purpura: A study of 11 cases
-
In press
-
Fakhouri F, Vernant JP, Veyradier A, et al. Efficiency of curative and prophylactic treatment with rituximab in ADAMTS13 deficient-thrombotic thrombocytopenic purpura: a study of 11 cases. Blood 2005. In press
-
(2005)
Blood
-
-
Fakhouri, F.1
Vernant, J.P.2
Veyradier, A.3
-
149
-
-
0030586446
-
Splenectomy done during hematologic remission to prevent relapse in patients with thrombotic thrombocytopenic purpura
-
Crowther MA, Heddle N, Hayward CP, Warkentin T, Kelton JG. Splenectomy done during hematologic remission to prevent relapse in patients with thrombotic thrombocytopenic purpura. Ann Intern Med 1996;125: 294-296
-
(1996)
Ann Intern Med
, vol.125
, pp. 294-296
-
-
Crowther, M.A.1
Heddle, N.2
Hayward, C.P.3
Warkentin, T.4
Kelton, J.G.5
-
150
-
-
0026787292
-
Thrombotic microangiopathies in the 1980s: Clinical features, response to treatment, and the impact of the human immunodeficiency virus epidemic
-
Thompson CE, Damon LE, Ries CA, Linker CA. Thrombotic microangiopathies in the 1980s: clinical features, response to treatment, and the impact of the human immunodeficiency virus epidemic. Blood 1992;80: 1890-1895
-
(1992)
Blood
, vol.80
, pp. 1890-1895
-
-
Thompson, C.E.1
Damon, L.E.2
Ries, C.A.3
Linker, C.A.4
-
151
-
-
0034760331
-
Laparoscopic splenectomy in patients with refractory or relapsing thrombotic thrombocytopenic purpura
-
Schwartz J, Eldor A, Szold A. Laparoscopic splenectomy in patients with refractory or relapsing thrombotic thrombocytopenic purpura. Arch Surg 2001;136:1236-1238
-
(2001)
Arch Surg
, vol.136
, pp. 1236-1238
-
-
Schwartz, J.1
Eldor, A.2
Szold, A.3
|