Miyata T - Search Results

1

Clinical significance of activated protein C resistance as a potential marker for hypercoagulable state.

Sakata T, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T. Sakata T, et al. Among authors: miyata t. Thromb Res. 1996 May 1;82(3):235-44. doi: 10.1016/0049-3848(96)00070-9. Thromb Res. 1996. PMID: 8732627

2

Recurrent restenosis after percutaneous transluminal coronary angioplasty in a patient with congenital protein C deficiency and high activated factor VII level.

Sakata T, Goto Y, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T. Sakata T, et al. Among authors: miyata t. Thromb Res. 1996 Mar 15;81(6):687-91. doi: 10.1016/0049-3848(96)00046-1. Thromb Res. 1996. PMID: 8868520 No abstract available.

3

Genetic analysis of protein C deficiency in nineteen Japanese families: five recurrent defects can explain half of the deficiencies.

Miyata T, Sakata T, Yasumuro Y, Okamura T, Katsumi A, Saito H, Abe T, Shirahata A, Sakai M, Kato H. Miyata T, et al. Thromb Res. 1998 Nov 15;92(4):181-7. doi: 10.1016/s0049-3848(98)00131-5. Thromb Res. 1998. PMID: 9840027

4

Analysis of 45 episodes of arterial occlusive disease in Japanese patients with congenital protein C deficiency.

Sakata T, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T. Sakata T, et al. Among authors: miyata t. Thromb Res. 1999 Apr 15;94(2):69-78. doi: 10.1016/s0049-3848(98)00194-7. Thromb Res. 1999. PMID: 10230891

5

Age- and sex-related differences of plasma activated factor VII levels in children.

Sakata T, Yamamura T, Kario K, Katayama Y, Matsuyama T, Kato H, Yamamoto A, Miyata T. Sakata T, et al. Among authors: miyata t. Thromb Haemost. 1999 Jun;81(6):910-2. Thromb Haemost. 1999. PMID: 10404766

6

Common C677T polymorphism in the methylenetetrahydrofolate reductase gene increases the risk for deep vein thrombosis in patients with predisposition of thrombophilia.

Fujimura H, Kawasaki T, Sakata T, Ariyoshi H, Kato H, Monden M, Miyata T. Fujimura H, et al. Among authors: miyata t. Thromb Res. 2000 Apr 1;98(1):1-8. doi: 10.1016/s0049-3848(99)00231-5. Thromb Res. 2000. PMID: 10706928

7

Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases.

Sakata T, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T. Sakata T, et al. Among authors: miyata t. Semin Thromb Hemost. 2000;26(1):11-6. doi: 10.1055/s-2000-9796. Semin Thromb Hemost. 2000. PMID: 10805275

8

Potential of free-form TFPI and PAI-1 to be useful markers of early atherosclerosis in a Japanese general population (the Suita Study): association with the intimal-medial thickness of carotid arteries.

Sakata T, Mannami T, Baba S, Kokubo Y, Kario K, Okamoto A, Kumeda K, Ohkura N, Katayama Y, Miyata T, Tomoike H, Kato H. Sakata T, et al. Among authors: miyata t. Atherosclerosis. 2004 Oct;176(2):355-60. doi: 10.1016/j.atherosclerosis.2004.05.017. Atherosclerosis. 2004. PMID: 15380459

9

Genetic risk factors for deep vein thrombosis among Japanese: importance of protein S K196E mutation.

Miyata T, Kimura R, Kokubo Y, Sakata T. Miyata T, et al. Int J Hematol. 2006 Apr;83(3):217-23. doi: 10.1532/IJH97.A20514. Int J Hematol. 2006. PMID: 16720551 Review.

10

A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.

Yin T, Takeshita S, Sato Y, Sakata T, Shin Y, Honda S, Kawasaki T, Tsuji H, Kojima T, Madoiwa S, Sakata Y, Murata M, Ikeda Y, Miyata T. Yin T, et al. Among authors: miyata t. Thromb Haemost. 2007 Oct;98(4):783-9. doi: 10.1160/th07-03-0211. Thromb Haemost. 2007. PMID: 17938802

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