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2,170 results

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Page 1
Multiplex fusion gene testing in pediatric acute myeloid leukemia.
Iijima-Yamashita Y, Matsuo H, Yamada M, Deguchi T, Kiyokawa N, Shimada A, Tawa A, Takahashi H, Tomizawa D, Taga T, Kinoshita A, Adachi S, Horibe K. Iijima-Yamashita Y, et al. Among authors: adachi s. Pediatr Int. 2018 Jan;60(1):47-51. doi: 10.1111/ped.13451. Pediatr Int. 2018. PMID: 29105243
Acute myeloid leukemia with multilineage dysplasia in children.
Adachi S, Manabe A, Imaizumi M, Taga T, Tawa A, Tsurusawa M, Kikuchi A, Masunaga A, Tsuchida M, Nakahata T; MDS Committee of the Japanese Society of Pediatric Hematology. Adachi S, et al. Int J Hematol. 2007 Nov;86(4):358-63. doi: 10.1532/IJH97.07025. Int J Hematol. 2007. PMID: 18055345
[Effectiveness of remission induction with high-dose cytarabine for relapsed or refractory pediatric acute leukemia].
Horikoshi Y, Kobayashi R, Endo M, Watanabe A, Kikuta A, Koike K, Hanada R, Hosoya R, Ohara A, Ikuta K, Goto H, Asami K, Sugita K, Horibe K, Tsurusawa M, Hori T, Hara J, Nishimura S, Nagatoshi Y, Mugishima H, Ohta S, Adachi S, Tsukimoto I. Horikoshi Y, et al. Among authors: adachi s. Rinsho Ketsueki. 2010 Feb;51(2):104-13. Rinsho Ketsueki. 2010. PMID: 20379101 Clinical Trial. Japanese.
Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group.
Mizushima Y, Taki T, Shimada A, Yui Y, Hiraumi Y, Matsubara H, Watanabe M, Watanabe K, Kamitsuji Y, Hayashi Y, Tsukimoto I, Kobayashi R, Horibe K, Tawa A, Nakahata T, Adachi S. Mizushima Y, et al. Among authors: adachi s. Int J Hematol. 2010 Jun;91(5):831-7. doi: 10.1007/s12185-010-0585-x. Epub 2010 May 22. Int J Hematol. 2010. PMID: 20495894
Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia.
Kanezaki R, Toki T, Terui K, Xu G, Wang R, Shimada A, Hama A, Kanegane H, Kawakami K, Endo M, Hasegawa D, Kogawa K, Adachi S, Ikeda Y, Iwamoto S, Taga T, Kosaka Y, Kojima S, Hayashi Y, Ito E. Kanezaki R, et al. Among authors: adachi s. Blood. 2010 Nov 25;116(22):4631-8. doi: 10.1182/blood-2010-05-282426. Epub 2010 Aug 20. Blood. 2010. PMID: 20729467 Free article.
DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.
Shiba N, Taki T, Park MJ, Shimada A, Sotomatsu M, Adachi S, Tawa A, Horibe K, Tsuchida M, Hanada R, Tsukimoto I, Arakawa H, Hayashi Y. Shiba N, et al. Among authors: adachi s. Br J Haematol. 2012 Feb;156(3):413-4. doi: 10.1111/j.1365-2141.2011.08879.x. Epub 2011 Oct 8. Br J Haematol. 2012. PMID: 21981547 Free article. No abstract available.
Pediatric idiopathic TTP diagnosed with decreased ADAMTS13 activity.
Morishima T, Nomura A, Saida S, Watanabe K, Yagi H, Matsumoto M, Fujimura Y, Heike T, Nakahata T, Adachi S. Morishima T, et al. Among authors: adachi s. Pediatr Int. 2012 Jun;54(3):422-3. doi: 10.1111/j.1442-200X.2011.03467.x. Pediatr Int. 2012. PMID: 22631573 No abstract available.
Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel.
Creutzig U, van den Heuvel-Eibrink MM, Gibson B, Dworzak MN, Adachi S, de Bont E, Harbott J, Hasle H, Johnston D, Kinoshita A, Lehrnbecher T, Leverger G, Mejstrikova E, Meshinchi S, Pession A, Raimondi SC, Sung L, Stary J, Zwaan CM, Kaspers GJ, Reinhardt D; AML Committee of the International BFM Study Group. Creutzig U, et al. Among authors: adachi s. Blood. 2012 Oct 18;120(16):3187-205. doi: 10.1182/blood-2012-03-362608. Epub 2012 Aug 9. Blood. 2012. PMID: 22879540 Free article. Review.
2,170 results