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Year Number of Results
2002 1
2010 4
2011 11
2012 11
2013 4
2014 2
2015 4
2017 2
2018 3
2019 2
2024 0

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33 results

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Page 1
Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophy.
Kato K, Maemura R, Wakamatsu M, Yamamori A, Hamada M, Kataoka S, Narita A, Miwata S, Sekiya Y, Kawashima N, Suzuki K, Narita K, Doisaki S, Muramatsu H, Sakaguchi H, Matsumoto K, Koike Y, Onodera O, Kaga M, Shimozawa N, Yoshida N. Kato K, et al. Among authors: doisaki s. Mol Genet Metab Rep. 2018 Nov 20;18:1-6. doi: 10.1016/j.ymgmr.2018.11.001. eCollection 2019 Mar. Mol Genet Metab Rep. 2018. PMID: 30519529 Free PMC article.
Molecular lesions in childhood and adult acute megakaryoblastic leukaemia.
Hama A, Muramatsu H, Makishima H, Sugimoto Y, Szpurka H, Jasek M, O'Keefe C, Takahashi Y, Sakaguchi H, Doisaki S, Shimada A, Watanabe N, Kato K, Kiyoi H, Naoe T, Kojima S, Maciejewski JP. Hama A, et al. Among authors: doisaki s. Br J Haematol. 2012 Feb;156(3):316-25. doi: 10.1111/j.1365-2141.2011.08948.x. Epub 2011 Nov 28. Br J Haematol. 2012. PMID: 22122069 Free article.
Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
Muramatsu H, Okuno Y, Yoshida K, Shiraishi Y, Doisaki S, Narita A, Sakaguchi H, Kawashima N, Wang X, Xu Y, Chiba K, Tanaka H, Hama A, Sanada M, Takahashi Y, Kanno H, Yamaguchi H, Ohga S, Manabe A, Harigae H, Kunishima S, Ishii E, Kobayashi M, Koike K, Watanabe K, Ito E, Takata M, Yabe M, Ogawa S, Miyano S, Kojima S. Muramatsu H, et al. Among authors: doisaki s. Genet Med. 2017 Jul;19(7):796-802. doi: 10.1038/gim.2016.197. Epub 2017 Jan 19. Genet Med. 2017. PMID: 28102861 Free article.
GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies.
Wang X, Muramatsu H, Okuno Y, Sakaguchi H, Yoshida K, Kawashima N, Xu Y, Shiraishi Y, Chiba K, Tanaka H, Saito S, Nakazawa Y, Masunari T, Hirose T, Elmahdi S, Narita A, Doisaki S, Ismael O, Makishima H, Hama A, Miyano S, Takahashi Y, Ogawa S, Kojima S. Wang X, et al. Among authors: doisaki s. Haematologica. 2015 Oct;100(10):e398-401. doi: 10.3324/haematol.2015.127092. Epub 2015 May 28. Haematologica. 2015. PMID: 26022708 Free PMC article. No abstract available.
Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation.
Takagi M, Shinoda K, Piao J, Mitsuiki N, Takagi M, Matsuda K, Muramatsu H, Doisaki S, Nagasawa M, Morio T, Kasahara Y, Koike K, Kojima S, Takao A, Mizutani S. Takagi M, et al. Among authors: doisaki s. Blood. 2011 Mar 10;117(10):2887-90. doi: 10.1182/blood-2010-08-301515. Epub 2010 Nov 9. Blood. 2011. PMID: 21063026 Free article.
Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children.
Wang X, Muramatsu H, Sakaguchi H, Xu Y, Narita A, Tsumura Y, Doisaki S, Tanaka M, Ismael O, Shimada A, Hama A, Takahashi Y, Kojima S. Wang X, et al. Among authors: doisaki s. Br J Haematol. 2012 Aug;158(4):553-5. doi: 10.1111/j.1365-2141.2012.09185.x. Epub 2012 Jun 12. Br J Haematol. 2012. PMID: 22686250 Free article. No abstract available.
Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.
Sakaguchi H, Okuno Y, Muramatsu H, Yoshida K, Shiraishi Y, Takahashi M, Kon A, Sanada M, Chiba K, Tanaka H, Makishima H, Wang X, Xu Y, Doisaki S, Hama A, Nakanishi K, Takahashi Y, Yoshida N, Maciejewski JP, Miyano S, Ogawa S, Kojima S. Sakaguchi H, et al. Among authors: doisaki s. Nat Genet. 2013 Aug;45(8):937-41. doi: 10.1038/ng.2698. Epub 2013 Jul 7. Nat Genet. 2013. PMID: 23832011
33 results