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Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome.
Matsumoto M, Kokame K, Soejima K, Miura M, Hayashi S, Fujii Y, Iwai A, Ito E, Tsuji Y, Takeda-Shitaka M, Iwadate M, Umeyama H, Yagi H, Ishizashi H, Banno F, Nakagaki T, Miyata T, Fujimura Y. Matsumoto M, et al. Among authors: miyata t. Blood. 2004 Feb 15;103(4):1305-10. doi: 10.1182/blood-2003-06-1796. Epub 2003 Oct 16. Blood. 2004. PMID: 14563640 Free article.
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. Fujimura Y, et al. Among authors: miyata t. Br J Haematol. 2009 Mar;144(5):742-54. doi: 10.1111/j.1365-2141.2008.07515.x. Epub 2008 Nov 26. Br J Haematol. 2009. PMID: 19055667 Free article.
Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) 2017 in Japan.
Matsumoto M, Fujimura Y, Wada H, Kokame K, Miyakawa Y, Ueda Y, Higasa S, Moriki T, Yagi H, Miyata T, Murata M; For TTP group of Blood Coagulation Abnormalities Research Team, Research on Rare and Intractable Disease supported by Health, Labour, and Welfare Sciences Research Grants. Matsumoto M, et al. Among authors: miyata t. Int J Hematol. 2017 Jul;106(1):3-15. doi: 10.1007/s12185-017-2264-7. Epub 2017 May 26. Int J Hematol. 2017. PMID: 28550351
Success and limitations of plasma treatment in pregnant women with congenital thrombotic thrombocytopenic purpura.
Sakai K, Fujimura Y, Nagata Y, Higasa S, Moriyama M, Isonishi A, Konno M, Kajiwara M, Ogawa Y, Kaburagi S, Hara T, Kokame K, Miyata T, Hatakeyama K, Matsumoto M. Sakai K, et al. Among authors: miyata t. J Thromb Haemost. 2020 Nov;18(11):2929-2941. doi: 10.1111/jth.15064. Epub 2020 Oct 15. J Thromb Haemost. 2020. PMID: 33433066 Free article.
ADAMTS13 activity and genetic mutations in Japan.
Miyata T, Kokame K, Matsumoto M, Fujimura Y. Miyata T, et al. Hamostaseologie. 2013 May 29;33(2):131-7. doi: 10.5482/HAMO-12-11-0017. Hamostaseologie. 2013. PMID: 23715102 Review.
2,229 results