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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.
Historical hematology: May-Hegglin anomaly.
Saito H, Kunishima S. Saito H, et al. Am J Hematol. 2008 Apr;83(4):304-6. doi: 10.1002/ajh.21102. Am J Hematol. 2008. PMID: 17975807 Free article.
ACTN1 mutations cause congenital macrothrombocytopenia.
Kunishima S, Okuno Y, Yoshida K, Shiraishi Y, Sanada M, Muramatsu H, Chiba K, Tanaka H, Miyazaki K, Sakai M, Ohtake M, Kobayashi R, Iguchi A, Niimi G, Otsu M, Takahashi Y, Miyano S, Saito H, Kojima S, Ogawa S. Kunishima S, et al. Among authors: saito h. Am J Hum Genet. 2013 Mar 7;92(3):431-8. doi: 10.1016/j.ajhg.2013.01.015. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434115 Free PMC article.
Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.
Suzuki N, Kunishima S, Ikejiri M, Maruyama S, Sone M, Takagi A, Ikawa M, Okabe M, Kojima T, Saito H, Naoe T, Matsushita T. Suzuki N, et al. Among authors: saito h. PLoS One. 2013 Aug 20;8(8):e71187. doi: 10.1371/journal.pone.0071187. eCollection 2013. PLoS One. 2013. PMID: 23976996 Free PMC article.
8,501 results