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10. High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence. von Krogh AS; Quist-Paulsen P; Waage A; Langseth ØO; Thorstensen K; Brudevold R; Tjønnfjord GE; Largiadèr CR; Lämmle B; Kremer Hovinga JA J Thromb Haemost; 2016 Jan; 14(1):73-82. PubMed ID: 26566785 [TBL] [Abstract][Full Text] [Related]
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12. 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]
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17. [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]
18. A phenotype-genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. Camilleri RS; Scully M; Thomas M; Mackie IJ; Liesner R; Chen WJ; Manns K; Machin SJ J Thromb Haemost; 2012 Sep; 10(9):1792-801. PubMed ID: 22783805 [TBL] [Abstract][Full Text] [Related]
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20. 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] [Next] [New Search]