Morio T - Search Results

1

Conditioning regimens for inborn errors of immunity: current perspectives and future strategies.

Nishimura A, Miyamoto S, Imai K, Morio T. Nishimura A, et al. Among authors: morio t. Int J Hematol. 2022 Jul;116(1):7-15. doi: 10.1007/s12185-022-03389-7. Epub 2022 Jun 8. Int J Hematol. 2022. PMID: 35675025 Review.

2

Clinical course of patients with WASP gene mutations.

Imai K, Morio T, Zhu Y, Jin Y, Itoh S, Kajiwara M, Yata J, Mizutani S, Ochs HD, Nonoyama S. Imai K, et al. Among authors: morio t. Blood. 2004 Jan 15;103(2):456-64. doi: 10.1182/blood-2003-05-1480. Epub 2003 Sep 11. Blood. 2004. PMID: 12969986 Free article.

3

Allogeneic hematopoietic stem cell transplantation for seven children with X-linked hyper-IgM syndrome: a single center experience.

Tomizawa D, Imai K, Ito S, Kajiwara M, Minegishi Y, Nagasawa M, Morio T, Nonoyama S, Mizutani S. Tomizawa D, et al. Among authors: morio t. Am J Hematol. 2004 May;76(1):33-9. doi: 10.1002/ajh.20044. Am J Hematol. 2004. PMID: 15114594 Free article.

4

Phenotypic variations between affected siblings with ataxia-telangiectasia: ataxia-telangiectasia in Japan.

Morio T, Takahashi N, Watanabe F, Honda F, Sato M, Takagi M, Imadome KI, Miyawaki T, Delia D, Nakamura K, Gatti RA, Mizutani S. Morio T, et al. Int J Hematol. 2009 Nov;90(4):455-462. doi: 10.1007/s12185-009-0408-0. Epub 2009 Aug 25. Int J Hematol. 2009. PMID: 19705055

5

Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma.

Uchisaka N, Takahashi N, Sato M, Kikuchi A, Mochizuki S, Imai K, Nonoyama S, Ohara O, Watanabe F, Mizutani S, Hanada R, Morio T. Uchisaka N, et al. Among authors: morio t. J Pediatr. 2009 Sep;155(3):435-8. doi: 10.1016/j.jpeds.2009.02.037. J Pediatr. 2009. PMID: 19732584

6

Analysis of mutations and recombination activity in RAG-deficient patients.

Asai E, Wada T, Sakakibara Y, Toga A, Toma T, Shimizu T, Nampoothiri S, Imai K, Nonoyama S, Morio T, Muramatsu H, Kamachi Y, Ohara O, Yachie A. Asai E, et al. Among authors: morio t. Clin Immunol. 2011 Feb;138(2):172-7. doi: 10.1016/j.clim.2010.11.005. Epub 2010 Dec 4. Clin Immunol. 2011. PMID: 21131235

7

Morio T, Atsuta Y, Tomizawa D, Nagamura-Inoue T, Kato K, Ariga T, Kawa K, Koike K, Tauchi H, Kajiwara M, Hara T, Kato S; Japanese Cord Blood Bank Network. Morio T, et al. Br J Haematol. 2011 Aug;154(3):363-72. doi: 10.1111/j.1365-2141.2011.08735.x. Epub 2011 May 14. Br J Haematol. 2011. PMID: 21569009 Free article.

8

Endocrine complications in primary immunodeficiency diseases in Japan.

Nozaki T, Takada H, Ishimura M, Ihara K, Imai K, Morio T, Kobayashi M, Nonoyama S, Hara T. Nozaki T, et al. Among authors: morio t. Clin Endocrinol (Oxf). 2012 Oct;77(4):628-34. doi: 10.1111/j.1365-2265.2012.04390.x. Clin Endocrinol (Oxf). 2012. PMID: 22432851

9

A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpura.

Kawasaki Y, Toyoda H, Otsuki S, Iwasa T, Iwamoto S, Azuma E, Itoh-Habe N, Wada H, Fujimura Y, Morio T, Imai K, Mitsuiki N, Ohara O, Komada Y. Kawasaki Y, et al. Among authors: morio t. Eur J Haematol. 2013 Feb;90(2):164-8. doi: 10.1111/ejh.12057. Epub 2013 Jan 7. Eur J Haematol. 2013. PMID: 23237501

10

Irreversible leukoencephalopathy after reduced-intensity stem cell transplantation in a dyskeratosis congenita patient with TINF2 mutation.

Isoda T, Mitsuiki N, Ohkawa T, Kaneko S, Endo A, Ono T, Aoki Y, Tomizawa D, Kajiwara M, Araki S, Nagasawa M, Morio T, Takagi M, Mizutani S. Isoda T, et al. Among authors: morio t. J Pediatr Hematol Oncol. 2013 May;35(4):e178-82. doi: 10.1097/MPH.0b013e318279e5ca. J Pediatr Hematol Oncol. 2013. PMID: 23242325

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