404 related articles for article (PubMed ID: 11843286)
21. 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; Cloarec S; Nivet H; Foulard M; Lesure F; Delattre P; Lakhdari M; Meyer D; Girma JP; Loirat C
J Pediatr; 2003 Mar; 142(3):310-7. PubMed ID: 12640381
[TBL] [Abstract][Full Text] [Related]
22. Platelets: thrombotic thrombocytopenic purpura.
George JN; Sadler JE; Lämmle B
Hematology Am Soc Hematol Educ Program; 2002; ():315-34. PubMed ID: 12446430
[TBL] [Abstract][Full Text] [Related]
23. ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage.
Soejima K; Matsumoto M; Kokame K; Yagi H; Ishizashi H; Maeda H; Nozaki C; Miyata T; Fujimura Y; Nakagaki T
Blood; 2003 Nov; 102(9):3232-7. PubMed ID: 12869506
[TBL] [Abstract][Full Text] [Related]
24. [Genetic polymorphism of von Willebrand factor (VWF)-cleaving protease, ADAMTS13].
Kokame K
Brain Nerve; 2008 Nov; 60(11):1325-32. PubMed ID: 19069166
[TBL] [Abstract][Full Text] [Related]
25. 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; Hutchins GM; Vogelsang GB; Tsai HM
Hematol J; 2001; 2(5):292-9. PubMed ID: 11920264
[TBL] [Abstract][Full Text] [Related]
26. Molecular mechanisms in thrombotic thrombocytopenic purpura.
Tsai HM
Semin Thromb Hemost; 2004 Oct; 30(5):549-57. PubMed ID: 15497097
[TBL] [Abstract][Full Text] [Related]
27. A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor-cleaving protease?
Soejima K; Mimura N; Hirashima M; Maeda H; Hamamoto T; Nakagaki T; Nozaki C
J Biochem; 2001 Oct; 130(4):475-80. PubMed ID: 11574066
[TBL] [Abstract][Full Text] [Related]
28. Inherited thrombotic thrombocytopenic purpura in pregnancy.
Drews K; Seremak-Mrozikiewicz A; Sobieszczyk S; Barlik M
Neuro Endocrinol Lett; 2013; 34(6):508-13. PubMed ID: 24378452
[TBL] [Abstract][Full Text] [Related]
29. Congenital microangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease.
Savaşan S; Taub JW; Buck S; Botterill M; Furlan M; Ravindranath Y
J Pediatr Hematol Oncol; 2001; 23(6):364-7. PubMed ID: 11563771
[TBL] [Abstract][Full Text] [Related]
30. A perspective on the measurement of ADAMTS13 in thrombotic thrombocytopaenic purpura.
Pimanda JE; Chesterman CN; Hogg PJ
Eur J Haematol; 2003 Apr; 70(4):257-62. PubMed ID: 12656756
[TBL] [Abstract][Full Text] [Related]
31. Deficiency of ADAMTS13 in thrombotic thrombocytopenic purpura.
Tsai HM
Int J Hematol; 2002 Aug; 76 Suppl 2():132-8. PubMed ID: 12430913
[TBL] [Abstract][Full Text] [Related]
32. Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.
Rank CU; Kremer Hovinga J; Taleghani MM; Lämmle B; Gøtze JP; Nielsen OJ
Eur J Haematol; 2014 Feb; 92(2):168-71. PubMed ID: 24033710
[TBL] [Abstract][Full Text] [Related]
33. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura.
Furlan M; Robles R; Solenthaler M; Wassmer M; Sandoz P; Lämmle B
Blood; 1997 May; 89(9):3097-103. PubMed ID: 9129011
[TBL] [Abstract][Full Text] [Related]
34. Molecular basis of ADAMTS13 dysfunction in thrombotic thrombocytopenic purpura.
Manea M; Karpman D
Pediatr Nephrol; 2009 Mar; 24(3):447-58. PubMed ID: 18807073
[TBL] [Abstract][Full Text] [Related]
35. Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.
Zheng X; Nishio K; Majerus EM; Sadler JE
J Biol Chem; 2003 Aug; 278(32):30136-41. PubMed ID: 12791682
[TBL] [Abstract][Full Text] [Related]
36. [ADAMTS13, von Willebrand factor specific cleaving protease].
Veyradier A; Coppo P
Med Sci (Paris); 2011 Dec; 27(12):1097-105. PubMed ID: 22192749
[TBL] [Abstract][Full Text] [Related]
37. Deficiency of von Willebrand factor-cleaving protease in familial and acquired thrombotic thrombocytopenic purpura.
Furlan M; Lämmle B
Baillieres Clin Haematol; 1998 Jun; 11(2):509-14. PubMed ID: 10097823
[TBL] [Abstract][Full Text] [Related]
38. von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura.
Moake JL
Semin Hematol; 2004 Jan; 41(1):4-14. PubMed ID: 14727254
[TBL] [Abstract][Full Text] [Related]
39. Molecular biology of ADAMTS13 and diagnostic utility of ADAMTS13 proteolytic activity and inhibitor assays.
Shelat SG; Ai J; Zheng XL
Semin Thromb Hemost; 2005 Dec; 31(6):659-72. PubMed ID: 16388417
[TBL] [Abstract][Full Text] [Related]
40. Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Veyradier A; Lavergne JM; Ribba AS; Obert B; Loirat C; Meyer D; Girma JP
J Thromb Haemost; 2004 Mar; 2(3):424-9. PubMed ID: 15009458
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]