309 related articles for article (PubMed ID: 25242241)
21. Paradigm shift of childhood thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency.
Yagi H; Matsumoto M; Fujimura Y
Presse Med; 2012 Mar; 41(3 Pt 2):e137-55. PubMed ID: 22264931
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Upshaw-Schulman syndrome revisited: a concept of congenital thrombotic thrombocytopenic purpura.
Kinoshita S; Yoshioka A; Park YD; Ishizashi H; Konno M; Funato M; Matsui T; Titani K; Yagi H; Matsumoto M; Fujimura Y
Int J Hematol; 2001 Jul; 74(1):101-8. PubMed ID: 11530798
[TBL] [Abstract][Full Text] [Related]
24. Inherited ADAMTS13 deficiency: unique presentation and treatment.
Born H; Peters A; Ettinger R
Pediatr Blood Cancer; 2008 May; 50(5):956-7. PubMed ID: 18240172
[TBL] [Abstract][Full Text] [Related]
25. Thrombotic thrombocytopenic purpura in pediatric patients.
Steele M; Chen HH; Steele J; Chan AK; Lau KK
Zhongguo Dang Dai Er Ke Za Zhi; 2012 Nov; 14(11):803-10. PubMed ID: 23146723
[TBL] [Abstract][Full Text] [Related]
26. Two novel heterozygote missense mutations of the ADAMTS13 gene in a child with recurrent thrombotic thrombocytopenic purpura.
Rossio R; Ferrari B; Cairo A; Mancini I; Pisapia G; Palazzo G; Peyvandi F
Blood Transfus; 2013 Apr; 11(2):241-4. PubMed ID: 23058857
[TBL] [Abstract][Full Text] [Related]
27. Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Hommais A; Rayes J; Houllier A; Obert B; Legendre P; Veyradier A; Girma JP; Ribba AS
Thromb Haemost; 2007 Sep; 98(3):593-9. PubMed ID: 17849048
[TBL] [Abstract][Full Text] [Related]
28. Congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) caused by novel ADAMTS13 mutations.
Kim HY; Lee KO; Yoo KH; Kim SH; Oh D; Kim HJ
Br J Haematol; 2016 Apr; 173(1):156-9. PubMed ID: 26085195
[No Abstract] [Full Text] [Related]
29. A successfully treated case of an acute presentation of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) with decreased ADAMTS13 during late stage of pregnancy.
Nonaka T; Yamaguchi M; Nishijima K; Moriyama M; Takakuwa K; Enomoto T
J Obstet Gynaecol Res; 2021 May; 47(5):1892-1897. PubMed ID: 33751717
[TBL] [Abstract][Full Text] [Related]
30. [From gene to disease; congenital thrombotic thrombocytopenic purpura due to mutations in the ADAMTS13 gene].
Schiphorst RH; van de Kar NC; van den Heuvel LP
Ned Tijdschr Geneeskd; 2003 Dec; 147(49):2422-4. PubMed ID: 14694551
[TBL] [Abstract][Full Text] [Related]
31. A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13.
Meyer SC; Jeddi R; Meddeb B; Gouider E; Lämmle B; Kremer Hovinga JA
Ann Hematol; 2008 Aug; 87(8):663-6. PubMed ID: 18443791
[TBL] [Abstract][Full Text] [Related]
32. Pregnancy-induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw-Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients.
Fujimura Y; Matsumoto M; Kokame K; Isonishi A; Soejima K; Akiyama N; Tomiyama J; Natori K; Kuranishi Y; Imamura Y; Inoue N; Higasa S; Seike M; Kozuka T; Hara M; Wada H; Murata M; Ikeda Y; Miyata T; George JN
Br J Haematol; 2009 Mar; 144(5):742-54. PubMed ID: 19055667
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura.
Kremer Hovinga JA; Lämmle B
Hematology Am Soc Hematol Educ Program; 2012; 2012():610-6. PubMed ID: 23233642
[TBL] [Abstract][Full Text] [Related]
35. Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura.
Moatti-Cohen M; Garrec C; Wolf M; Boisseau P; Galicier L; Azoulay E; Stepanian A; Delmas Y; Rondeau E; Bezieau S; Coppo P; Veyradier A;
Blood; 2012 Jun; 119(24):5888-97. PubMed ID: 22547583
[TBL] [Abstract][Full Text] [Related]
36. TTP and ADAMTS13: When Is Testing Appropriate?
Mannucci PM; Peyvandi F
Hematology Am Soc Hematol Educ Program; 2007; ():121-6. PubMed ID: 18024619
[TBL] [Abstract][Full Text] [Related]
37. A case of severe ADAMTS13 deficiency presenting as thrombotic thrombocytopenic purpura in pregnancy.
Nikolaou M; Karakantza M; Adonakis G; Theodorou G; Zoumbos N; Decavalas G
Med Pregl; 2012; 65(9-10):436-9. PubMed ID: 23214340
[TBL] [Abstract][Full Text] [Related]
38. Low incidence of ADAMTS13 missense mutation R1060W in adult Egyptian patients with thrombotic thrombocytopenic purpura.
El Sissy MH; El Hafez AA; El Sissy AH
Acta Haematol; 2014; 132(1):30-5. PubMed ID: 24401653
[TBL] [Abstract][Full Text] [Related]
39. Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura.
Furlan M
Expert Rev Cardiovasc Ther; 2003 Jul; 1(2):243-55. PubMed ID: 15030284
[TBL] [Abstract][Full Text] [Related]
40. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry.
Mansouri Taleghani M; von Krogh AS; Fujimura Y; George JN; Hrachovinová I; Knöbl PN; Quist-Paulsen P; Schneppenheim R; Lämmle B; Kremer Hovinga JA
Hamostaseologie; 2013 May; 33(2):138-43. PubMed ID: 23715103
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]