Saito H - Search Results

1

Further characterization of anti-platelet monoclonal antibody HPL5 as anti-glycoprotein V antibody.

Kunishima S, Motoyama M, Takagi A, Hamaguchi M, Kojima T, Saito H. Kunishima S, et al. Among authors: saito h. Acta Haematol. 2006;115(1-2):128-30. doi: 10.1159/000089480. Acta Haematol. 2006. PMID: 16424664 No abstract available.

2

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.

Kunishima S, Sako M, Yamazaki T, Hamaguchi M, Saito H. Kunishima S, et al. Among authors: saito h. Eur J Haematol. 2006 Dec;77(6):501-12. doi: 10.1111/j.0902-4441.2006.t01-1-EJH2817.x. Epub 2006 Sep 15. Eur J Haematol. 2006. PMID: 16978236

3

Genetic abnormalities of Bernard-Soulier syndrome.

Kunishima S, Kamiya T, Saito H. Kunishima S, et al. Among authors: saito h. Int J Hematol. 2002 Nov;76(4):319-27. doi: 10.1007/BF02982690. Int J Hematol. 2002. PMID: 12463594 Review.

4

Congenital macrothrombocytopenias.

Kunishima S, Saito H. Kunishima S, et al. Among authors: saito h. Blood Rev. 2006 Mar;20(2):111-21. doi: 10.1016/j.blre.2005.08.001. Epub 2005 Sep 19. Blood Rev. 2006. PMID: 16169642 Review.

5

Novel heterozygous missense mutation in the second leucine rich repeat of GPIbalpha affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura.

Kunishima S, Imai T, Hamaguchi M, Saito H. Kunishima S, et al. Among authors: saito h. Eur J Haematol. 2006 Apr;76(4):348-55. doi: 10.1111/j.1600-0609.2005.00612.x. Eur J Haematol. 2006. PMID: 16519708

6

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.

Kunishima S, Yoshinari M, Nishio H, Ida K, Miura T, Matsushita T, Hamaguchi M, Saito H. Kunishima S, et al. Among authors: saito h. Eur J Haematol. 2007 Mar;78(3):220-6. doi: 10.1111/j.1600-0609.2006.00806.x. Epub 2007 Jan 16. Eur J Haematol. 2007. PMID: 17241369

7

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.

Kunishima S, Hamaguchi M, Saito H. Kunishima S, et al. Among authors: saito h. Blood. 2008 Mar 15;111(6):3015-23. doi: 10.1182/blood-2007-10-116194. Epub 2008 Jan 11. Blood. 2008. PMID: 18192507 Free article.

8

Identification and characterization of the first large deletion of the MYH9 gene associated with MYH9 disorders.

Kunishima S, Matsushita T, Hamaguchi M, Saito H. Kunishima S, et al. Among authors: saito h. Eur J Haematol. 2008 Jun;80(6):540-4. doi: 10.1111/j.1600-0609.2008.01046.x. Epub 2008 Feb 13. Eur J Haematol. 2008. PMID: 18284620

9

Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion.

Kunishima S, Imai T, Kobayashi R, Kato M, Ogawa S, Saito H. Kunishima S, et al. Among authors: saito h. Pediatr Int. 2013 Aug;55(4):434-7. doi: 10.1111/ped.12105. Pediatr Int. 2013. PMID: 23566026

10

Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome.

Kunishima S, Matsushita T, Ito T, Kamiya T, Saito H. Kunishima S, et al. Among authors: saito h. Am J Hematol. 2002 Dec;71(4):279-84. doi: 10.1002/ajh.10230. Am J Hematol. 2002. PMID: 12447957 Free article.

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