175 related articles for article (PubMed ID: 23700827)
1. [Variety of thrombotic thrombocytopenic purpura clinical course in Polish family members with ADAMTS 13 gene mutation].
Hyla-Klekot L; Kucharska G; Słonka K
Pol Merkur Lekarski; 2013 Mar; 34(201):161-4. PubMed ID: 23700827
[TBL] [Abstract][Full Text] [Related]
2. The D173G mutation in ADAMTS-13 causes a severe form of congenital thrombotic thrombocytopenic purpura. A clinical, biochemical and in silico study.
Lancellotti S; Peyvandi F; Pagliari MT; Cairo A; Abdel-Azeim S; Chermak E; Lazzareschi I; Mastrangelo S; Cavallo L; Oliva R; De Cristofaro R
Thromb Haemost; 2016 Jan; 115(1):51-62. PubMed ID: 26272487
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children.
Loirat C; Girma JP; Desconclois C; Coppo P; Veyradier A
Pediatr Nephrol; 2009 Jan; 24(1):19-29. PubMed ID: 18574602
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. Clinical usefulness of a functional assay for the von Willebrand factor cleaving protease (ADAMTS 13) and its inhibitor in a patient with thrombotic thrombocytopenic purpura.
Rick ME; Austin H; Leitman SF; Krizek DM; Aronson DL
Am J Hematol; 2004 Feb; 75(2):96-100. PubMed ID: 14755376
[TBL] [Abstract][Full Text] [Related]
9. Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.
Pérez-Rodríguez A; Lourés E; Rodríguez-Trillo Á; Costa-Pinto J; García-Rivero A; Batlle-López A; Batlle J; López-Fernández MF
Thromb Res; 2014 Dec; 134(6):1171-5. PubMed ID: 25242241
[TBL] [Abstract][Full Text] [Related]
10. Novel compound heterozygote mutations (H234Q/R1206X) of the ADAMTS13 gene in an adult patient with Upshaw-Schulman syndrome showing predominant episodes of repeated acute renal failure.
Shibagaki Y; Matsumoto M; Kokame K; Ohba S; Miyata T; Fujimura Y; Fujita T
Nephrol Dial Transplant; 2006 May; 21(5):1289-92. PubMed ID: 16449289
[TBL] [Abstract][Full Text] [Related]
11. von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura.
Peyvandi F; Ferrari S; Lavoretano S; Canciani MT; Mannucci PM
Br J Haematol; 2004 Nov; 127(4):433-9. PubMed ID: 15521921
[TBL] [Abstract][Full Text] [Related]
12. The course of ADAMTS-13 activity and inhibitor titre in the treatment of thrombotic thrombocytopenic purpura with plasma exchange and vincristine.
Böhm M; Betz C; Miesbach W; Krause M; von Auer C; Geiger H; Scharrer I
Br J Haematol; 2005 Jun; 129(5):644-52. PubMed ID: 15916687
[TBL] [Abstract][Full Text] [Related]
13. Case of maternal and fetal deaths due to severe congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) during pregnancy.
Tanaka H; Tenkumo C; Mori N; Kokame K; Fujimura Y; Hata T
J Obstet Gynaecol Res; 2014 Jan; 40(1):247-9. PubMed ID: 23937165
[TBL] [Abstract][Full Text] [Related]
14. Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.
Klukowska A; Niewiadomska E; Budde U; Oyen F; Schneppenheim R
J Pediatr Hematol Oncol; 2010 Mar; 32(2):103-7. PubMed ID: 20118810
[TBL] [Abstract][Full Text] [Related]
15. Inherited thrombotic thrombocytopenic purpura in children.
Hassenpflug WA; Budde U; Schneppenheim S; Schneppenheim R
Semin Thromb Hemost; 2014 Jun; 40(4):487-92. PubMed ID: 24816970
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. Experiences in a family with the Upshaw-Schulman syndrome over a 44-year period.
Bennett M; Chubar Y; Gavish I; Aviv A; Stemer G; Chap-Marshak D
Clin Appl Thromb Hemost; 2014 Apr; 20(3):296-303. PubMed ID: 23872162
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura.
Camilleri RS; Cohen H; Mackie IJ; Scully M; Starke RD; Crawley JT; Lane DA; Machin SJ
J Thromb Haemost; 2008 Feb; 6(2):331-8. PubMed ID: 18031293
[TBL] [Abstract][Full Text] [Related]
20. [Hereditary form of thrombotic thrombocytopenic purpura].
Hrachovinová I; Rittich S; Salaj P; Suttnar J; Dyr JE; Suláková T; Pták J; Dulícek P; Seeman T
Cas Lek Cesk; 2006; 145(5):390-2. PubMed ID: 16755777
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
