Muramatsu H - Search Results

1

Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.

Ichimura T, Yoshida K, Okuno Y, Yujiri T, Nagai K, Nishi M, Shiraishi Y, Ueno H, Toki T, Chiba K, Tanaka H, Muramatsu H, Hara T, Kanno H, Kojima S, Miyano S, Ito E, Ogawa S, Ohga S. Ichimura T, et al. Among authors: muramatsu h. Int J Hematol. 2017 Apr;105(4):515-520. doi: 10.1007/s12185-016-2151-7. Epub 2016 Nov 23. Int J Hematol. 2017. PMID: 27882484

2

Wiskott-Aldrich syndrome is an important differential diagnosis in male infants with juvenile myelomonocytic leukemialike features.

Watanabe N, Yoshimi A, Kamachi Y, Kawabe T, Muramatsu H, Matsumoto K, Manabe A, Kojima S, Kato K. Watanabe N, et al. Among authors: muramatsu h. J Pediatr Hematol Oncol. 2007 Dec;29(12):836-8. doi: 10.1097/MPH.0b013e3181580ec5. J Pediatr Hematol Oncol. 2007. PMID: 18090932

3

Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome.

Hama A, Yagasaki H, Takahashi Y, Nishio N, Muramatsu H, Yoshida N, Tanaka M, Hidaka H, Watanabe N, Yoshimi A, Matsumoto K, Kudo K, Kato K, Horibe K, Kojima S. Hama A, et al. Among authors: muramatsu h. Br J Haematol. 2008 Mar;140(5):552-61. doi: 10.1111/j.1365-2141.2007.06971.x. Br J Haematol. 2008. PMID: 18275433 Free article.

4

[Anemia in children].

Muramatsu H, Kojima S. Muramatsu H, et al. Nihon Rinsho. 2008 Mar;66(3):544-7. Nihon Rinsho. 2008. PMID: 18326324 Review. Japanese.

5

Congenital erythroid and myeloid hypoplasia terminating myelodysplastic syndrome.

Nishio N, Yagasaki H, Takahashi Y, Muramatsu H, Hama A, Xu Y, Villalobos IB, Kojima S. Nishio N, et al. Among authors: muramatsu h. J Pediatr Hematol Oncol. 2008 Sep;30(9):692-5. doi: 10.1097/MPH.0b013e31816e23a1. J Pediatr Hematol Oncol. 2008. PMID: 18776763

6

Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia.

Yoshida N, Yagasaki H, Xu Y, Matsuda K, Yoshimi A, Takahashi Y, Hama A, Nishio N, Muramatsu H, Watanabe N, Matsumoto K, Kato K, Ueyama J, Inada H, Goto H, Yabe M, Kudo K, Mimaya J, Kikuchi A, Manabe A, Koike K, Kojima S. Yoshida N, et al. Among authors: muramatsu h. Pediatr Res. 2009 Mar;65(3):334-40. doi: 10.1203/PDR.0b013e3181961d2a. Pediatr Res. 2009. PMID: 19047918

7

Engraftment syndrome following allogeneic hematopoietic stem cell transplantation in children.

Nishio N, Yagasaki H, Takahashi Y, Hama A, Muramatsu H, Tanaka M, Yoshida N, Yoshimi A, Kudo K, Ito M, Kojima S. Nishio N, et al. Among authors: muramatsu h. Pediatr Transplant. 2009 Nov;13(7):831-7. doi: 10.1111/j.1399-3046.2008.01068.x. Epub 2008 Nov 1. Pediatr Transplant. 2009. PMID: 19067915

8

Concurrent Langerhans cell histiocytosis and nephroblastoma.

Narui R, Yagasaki H, Takahashi Y, Hama A, Nishio N, Muramatsu H, Shimoyama Y, Kojima S. Narui R, et al. Among authors: muramatsu h. Pediatr Blood Cancer. 2009 May;52(5):662-4. doi: 10.1002/pbc.21927. Pediatr Blood Cancer. 2009. PMID: 19148948

9

Natural history of transfusion-independent non-severe aplastic anemia in children.

Nishio N, Yagasaki H, Takahashi Y, Muramatsu H, Hama A, Yoshida N, Kudo K, Kojima S. Nishio N, et al. Among authors: muramatsu h. Int J Hematol. 2009 May;89(4):409-413. doi: 10.1007/s12185-009-0302-9. Epub 2009 Apr 3. Int J Hematol. 2009. PMID: 19343478

10

Plasmacytoid dendritic cell leukemia in children.

Hama A, Kudo K, Itzel BV, Muramatsu H, Nishio N, Yoshida N, Takahashi Y, Yagasaki H, Ito M, Kojima S. Hama A, et al. Among authors: muramatsu h. J Pediatr Hematol Oncol. 2009 May;31(5):339-43. doi: 10.1097/MPH.0b013e31819b7215. J Pediatr Hematol Oncol. 2009. PMID: 19415013

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