Iida H - Search Results

1

Characterization of two novel mutations of the antithrombin gene observed in Japanese thrombophilic patients.

Kurihara M, Watanabe K, Inoue S, Wada Y, Ono M, Wakiyama M, Iida H, Kinoshita S, Hamasaki N. Kurihara M, et al. Among authors: iida h. Thromb Res. 2005;115(5):351-8. doi: 10.1016/j.thromres.2004.08.025. Thromb Res. 2005. PMID: 15733967

2

Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: effects on secretion and anticoagulant activity of protein S.

Tsuda H, Urata M, Tsuda T, Wakiyama M, Iida H, Nakahara M, Kinoshita S, Hamasaki N. Tsuda H, et al. Among authors: iida h. Thromb Res. 2002 Feb 1;105(3):233-9. doi: 10.1016/s0049-3848(02)00015-4. Thromb Res. 2002. PMID: 11927129

3

Identification of simultaneous mutation of fibrinogen alpha chain and protein C genes in a Japanese kindred.

Watanabe K, Shibuya A, Ishii E, Kurihara M, Inoue S, Ono M, Wada Y, Wakiyama M, Zaitsu M, Iida H, Muraoka K, Kinoshita S, Hamasaki N. Watanabe K, et al. Among authors: iida h. Br J Haematol. 2003 Jan;120(1):101-8. doi: 10.1046/j.1365-2141.2003.03985.x. Br J Haematol. 2003. PMID: 12492584 Free article.

4

Protein S and protein C gene mutations in Japanese deep vein thrombosis patients.

Kinoshita S, Iida H, Inoue S, Watanabe K, Kurihara M, Wada Y, Tsuda H, Kang D, Hamasaki N. Kinoshita S, et al. Among authors: iida h. Clin Biochem. 2005 Oct;38(10):908-15. doi: 10.1016/j.clinbiochem.2005.05.006. Clin Biochem. 2005. PMID: 15978566

5

A novel splice acceptor site mutation of protein S gene in affected individuals with type I protein S deficiency: allelic exclusion of the mutant gene.

Nakahara M, Iida H, Urata M, Fujise M, Wakiyama M, Kinoshita S, Tsuda H, Okamura T, Yao K, Yao T, Hamasaki N. Nakahara M, et al. Among authors: iida h. Thromb Res. 2001 Mar 1;101(5):387-93. doi: 10.1016/s0049-3848(01)00210-9. Thromb Res. 2001. PMID: 11297755

6

Failure in the detection of aberrant mRNA from the heterozygotic splice site mutant allele for protein S in a patient with protein S deficiency.

Iida H, Nakahara M, Komori K, Fujise M, Wakiyama M, Urata M, Kinoshita S, Tsuda H, Sugimachi K, Hamasaki N. Iida H, et al. Thromb Res. 2001 May 1;102(3):187-96. doi: 10.1016/s0049-3848(01)00246-8. Thromb Res. 2001. PMID: 11369411

7

Analytical goals for coagulation tests based on biological variation.

Wada Y, Kurihara M, Toyofuku M, Kawamura M, Iida H, Kayamori Y, Kinoshita S, Hamasaki N. Wada Y, et al. Among authors: iida h. Clin Chem Lab Med. 2004 Jan;42(1):79-83. doi: 10.1515/CCLM.2004.015. Clin Chem Lab Med. 2004. PMID: 15061385

8

A novel splice acceptor site mutation which produces multiple splicing abnormalities resulting in protein S deficiency type I.

Tatewaki H, Iida H, Nakahara M, Tsuda H, Kinoshita S, Kanaji T, Yoshida N, Miyazaki S, Hamasaki N. Tatewaki H, et al. Among authors: iida h. Thromb Haemost. 1999 Jul;82(1):65-71. Thromb Haemost. 1999. PMID: 10456456

9

A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.

Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N. Iida H, et al. Thromb Haemost. 2000 Jul;84(1):49-53. Thromb Haemost. 2000. PMID: 10928469

10

[Molecular biology techniques as clinical laboratory tests].

Hamasaki N, Iida H, Kinoshita S. Hamasaki N, et al. Among authors: iida h. Rinsho Byori. 2001 Jan;49(1):9-18. Rinsho Byori. 2001. PMID: 11215491 Review. Japanese.

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