Thrombotic thrombocytopenic purpura

被引：2
作者：
Lämmle, B [1 ]
Hovinga, JK
Studt, JD
Taleghani, BM
Alberio, L
机构：
[1] Univ Hosp Bern, Dept Hematol, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Cent Hematol Lab, Inselspital, CH-3010 Bern, Switzerland
来源：
HEMATOLOGY JOURNAL | 2004年 / 5卷
关键词：
D O I：
10.1038/sj.thj.6200413
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：S6 / S11
页数：6
相关论文
共 36 条
  • [1] THROMBOTIC THROMBOCYTOPENIC PURPURA - REPORT OF 16 CASES AND REVIEW OF LITERATURE
    AMOROSI, EL
    ULTMANN, JE
    [J]. MEDICINE, 1966, 45 (02) : 139 - +
  • [2] ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13
    Antoine, G
    Zimmermann, K
    Plaimauer, B
    Grillowitzer, M
    Studt, JD
    Lämmle, B
    Scheiflinger, F
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (05) : 821 - 824
  • [3] Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders:: a severely deficient activity is specific for thrombotic thrombocytopenic purpura
    Bianchi, V
    Robles, R
    Alberio, L
    Furlan, M
    Lämmle, B
    [J]. BLOOD, 2002, 100 (02) : 710 - 713
  • [4] ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions
    Dong, JF
    Moake, JL
    Nolasco, L
    Bernardo, A
    Arceneaux, W
    Shrimpton, CN
    Schade, AJ
    McIntire, LV
    Fujikawa, K
    López, JA
    [J]. BLOOD, 2002, 100 (12) : 4033 - 4039
  • [5] Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family
    Fujikawa, K
    Suzuki, H
    McMullen, B
    Chung, D
    [J]. BLOOD, 2001, 98 (06) : 1662 - 1666
  • [6] Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
    Furlan, M
    Robles, R
    Solenthaler, M
    Wassmer, M
    Sandoz, P
    Lammle, B
    [J]. BLOOD, 1997, 89 (09) : 3097 - 3103
  • [7] Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
    Furlan, M
    Robles, R
    Solenthaler, M
    Lämmle, B
    [J]. BLOOD, 1998, 91 (08) : 2839 - 2846
  • [8] Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
    Furlan, M
    Robles, R
    Galbusera, M
    Remuzzi, G
    Kyrle, PA
    Brenner, B
    Krause, M
    Scharrer, I
    Aumann, V
    Mittler, U
    Solenthaler, M
    Lämmle, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (22) : 1578 - 1584
  • [9] Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome:: the role of von Willebrand factor-cleaving protease
    Furlan, M
    Lämmle, B
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2001, 14 (02) : 437 - 454
  • [10] How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
    George, JN
    [J]. BLOOD, 2000, 96 (04) : 1223 - 1229
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