Sato H - Search Results

1

Raccoon eyes in an infant with neuroblastoma.

Onoda T, Sato H, Meguro T, Mitsui T. Onoda T, et al. Among authors: sato h. Pediatr Int. 2021 Jul;63(7):863-864. doi: 10.1111/ped.14618. Pediatr Int. 2021. PMID: 34219341 No abstract available.

2

Eltrombopag with i.v. immunoglobulin for safe splenectomy in refractory immune thrombocytopenia.

Kanno M, Onoda T, Meguro T, Sato H, Mitsui T. Kanno M, et al. Among authors: sato h. Pediatr Int. 2018 Feb;60(2):191-192. doi: 10.1111/ped.13446. Epub 2017 Dec 22. Pediatr Int. 2018. PMID: 29271533 No abstract available.

3

[Successful treatment with sorafenib for primary refractory acute monoblastic leukemia with FLT3-ITD].

Takahashi N, Kawakami T, Sato H, Onoda T, Kanno M, Mitsui T, Hayasaka K. Takahashi N, et al. Among authors: sato h. Rinsho Ketsueki. 2012 Nov;53(11):1932-6. Rinsho Ketsueki. 2012. PMID: 23257676 Japanese.

4

Successful treatment of acute myeloid leukaemia in a patient with ataxia telangiectasia.

Onoda T, Kanno M, Meguro T, Sato H, Takahashi N, Kawakami T, Mitsui T, Hayasaka K. Onoda T, et al. Among authors: sato h. Eur J Haematol. 2013 Dec;91(6):557-60. doi: 10.1111/ejh.12186. Epub 2013 Sep 18. Eur J Haematol. 2013. PMID: 23952578

5

Identification of novel ALK rearrangement A2M-ALK in a neonate with fetal lung interstitial tumor.

Onoda T, Kanno M, Sato H, Takahashi N, Izumino H, Ohta H, Emura T, Katoh H, Ohizumi H, Ohtake H, Asao H, Dehner LP, Hill AD, Hayasaka K, Mitsui T. Onoda T, et al. Among authors: sato h. Genes Chromosomes Cancer. 2014 Oct;53(10):865-74. doi: 10.1002/gcc.22199. Epub 2014 Jun 26. Genes Chromosomes Cancer. 2014. PMID: 24965693

6

Three Consecutive Cases of Familial Hemophagocytic Lymphohistiocytosis, Including a Case Due to Maternal Uniparental Disomy.

Sato H, Kawasaki N, Kawasaki M, Abiko Y, Meguro T, Takahashi N, Izumino H, Kanno M, Numakura C, Sasaki A, Imamura T, Taki T, Mitsui T. Sato H, et al. J Pediatr Hematol Oncol. 2020 Nov;42(8):e819-e821. doi: 10.1097/MPH.0000000000001681. J Pediatr Hematol Oncol. 2020. PMID: 31789783

7

ALOX12 mutation in a family with dominantly inherited bleeding diathesis.

Mitsui T, Makino S, Tamiya G, Sato H, Kawakami Y, Takahashi Y, Meguro T, Izumino H, Sudo Y, Norota I, Ishii K, Hayasaka K. Mitsui T, et al. Among authors: sato h. J Hum Genet. 2021 Aug;66(8):753-759. doi: 10.1038/s10038-020-00887-6. Epub 2021 Feb 10. J Hum Genet. 2021. PMID: 33564083

8

Retrospective examination of coagulation parameters in 33 patients with autoimmune coagulation factor deficiencies in Japan: A single-center analysis.

Osaki T, Souri M, Ogawa Y, Sato H, Mitsui T, Ichinose A. Osaki T, et al. Among authors: sato h. Thromb Res. 2022 May;213:154-162. doi: 10.1016/j.thromres.2022.03.006. Epub 2022 Mar 10. Thromb Res. 2022. PMID: 35378421

9

[Examination of Measures for Preventing Exposure in Nurses Who Handle Cyclophosphamide].

Suzuki K, Ono Y, Suzuki Y, Omori K, Matsuda M, Sato H, Omoto E. Suzuki K, et al. Among authors: sato h. Gan To Kagaku Ryoho. 2015 Dec;42(13):2457-9. Gan To Kagaku Ryoho. 2015. PMID: 26809304 Japanese.

10

A case of primarily facial pyoderma gangrenosum associated with Takayasu arteritis.

Okamura K, Konno T, Onami K, Nikaido M, Okazaki N, Abe Y, Hayashi M, Yaguchi Y, Sato H, Konta T, Suzuki T. Okamura K, et al. Among authors: sato h. JAAD Case Rep. 2017 Mar 12;3(2):124-126. doi: 10.1016/j.jdcr.2016.12.006. eCollection 2017 Mar. JAAD Case Rep. 2017. PMID: 28331898 Free PMC article. No abstract available.

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