Meguro T - Search Results

1

Giant thymolipoma in a young child initially diagnosed as cardiomegaly.

Onoda T, Meguro T, Kanno M, Ohta H, Nakamura M, Ohtake H, Mitsui T. Onoda T, et al. Among authors: meguro t. Pediatr Int. 2015 Oct;57(5):1051-2. doi: 10.1111/ped.12786. Pediatr Int. 2015. PMID: 26508197 No abstract available.

2

Raccoon eyes in an infant with neuroblastoma.

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

3

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: meguro t. Eur J Haematol. 2013 Dec;91(6):557-60. doi: 10.1111/ejh.12186. Epub 2013 Sep 18. Eur J Haematol. 2013. PMID: 23952578

4

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. Among authors: meguro t. J Pediatr Hematol Oncol. 2020 Nov;42(8):e819-e821. doi: 10.1097/MPH.0000000000001681. J Pediatr Hematol Oncol. 2020. PMID: 31789783

5

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: meguro t. 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

6

A surgical case of pediatric spinal medulloepithelioma.

Nakamura K, Matsuda KI, Kabasawa T, Meguro T, Kurose A, Sonoda Y. Nakamura K, et al. Among authors: meguro t. Childs Nerv Syst. 2022 Feb;38(2):473-477. doi: 10.1007/s00381-021-05293-7. Epub 2021 Jul 26. Childs Nerv Syst. 2022. PMID: 34312708

7

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.

Meguro T, Yoshida Y, Hayashi M, Toyota K, Otagiri T, Mochizuki N, Kishikawa Y, Sasaki A, Hayasaka K. Meguro T, et al. J Hum Genet. 2012 May;57(5):335-7. doi: 10.1038/jhg.2012.27. Epub 2012 Mar 22. J Hum Genet. 2012. PMID: 22437207

8

Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome.

Shimokaze T, Sasaki A, Meguro T, Hasegawa H, Hiraku Y, Yoshikawa T, Kishikawa Y, Hayasaka K. Shimokaze T, et al. Among authors: meguro t. J Hum Genet. 2015 Sep;60(9):473-7. doi: 10.1038/jhg.2015.65. Epub 2015 Jun 11. J Hum Genet. 2015. PMID: 26063465

9

A retrospective analysis of azacitidine treatment for juvenile myelomonocytic leukemia.

Honda Y, Muramatsu H, Nanjo Y, Hirabayashi S, Meguro T, Yoshida N, Kakuda H, Ozono S, Wakamatsu M, Moritake H, Yasui M, Sano H, Manabe A, Sakashita K. Honda Y, et al. Among authors: meguro t. Int J Hematol. 2022 Feb;115(2):263-268. doi: 10.1007/s12185-021-03248-x. Epub 2021 Oct 29. Int J Hematol. 2022. PMID: 34714526

10

Efficacy and Safety of Durvalumab/Tremelimumab in Unresectable Hepatocellular Carcinoma as Immune Checkpoint Inhibitor Rechallenge Following Atezolizumab/Bevacizumab Treatment.

Sho T, Suda G, Ohara M, Kohya R, Sasaki T, Yoshida S, Hosoda S, Ogawa K, Kitagataya T, Maehara O, Ohnishi S, Kawagishi N, Natsuizaka M, Nakai M, Baba M, Yamamoto Y, Tsukuda Y, Meguro T, Yamada R, Kobayashi T, Takagi T, Sakamoto N; NORTE STUDY GROUP. Sho T, et al. Among authors: meguro t. Target Oncol. 2024 Sep;19(5):769-778. doi: 10.1007/s11523-024-01092-7. Epub 2024 Sep 2. Target Oncol. 2024. PMID: 39222223

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