Okada S - Search Results

1

Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency.

Kawai T, Nishikomori R, Izawa K, Murata Y, Tanaka N, Sakai H, Saito M, Yasumi T, Takaoka Y, Nakahata T, Mizukami T, Nunoi H, Kiyohara Y, Yoden A, Murata T, Sasaki S, Ito E, Akutagawa H, Kawai T, Imai C, Okada S, Kobayashi M, Heike T. Kawai T, et al. Among authors: okada s. Blood. 2012 Jun 7;119(23):5458-66. doi: 10.1182/blood-2011-05-354167. Epub 2012 Apr 19. Blood. 2012. PMID: 22517901 Free article.

2

A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia.

Sera Y, Kawaguchi H, Nakamura K, Sato T, Habara M, Okada S, Ishikawa N, Kojima S, Katoh O, Kobayashi M. Sera Y, et al. Among authors: okada s. Haematologica. 2005 Aug;90(8):1032-41. Haematologica. 2005. PMID: 16079102

3

[X-linked hypogammaglobulinemia with growth hormone deficiency].

Okada S, Miyagawa S, Nishimura S, Kobayashi M, Nishi Y. Okada S, et al. Nihon Rinsho. 2006 May 28;Suppl 1:67-9. Nihon Rinsho. 2006. PMID: 16776095 Review. Japanese. No abstract available.

4

Steroid-dependent ACTH-produced thymic carcinoid: regulation of POMC gene expression by cortisol via methylation of its promoter region.

Mizoguchi Y, Kajiume T, Miyagawa S, Okada S, Nishi Y, Kobayashi M. Mizoguchi Y, et al. Among authors: okada s. Horm Res. 2007;67(5):257-62. doi: 10.1159/000098548. Epub 2007 Jan 12. Horm Res. 2007. PMID: 17220632

5

A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients.

Ishikawa N, Okada S, Sato T, Yasunaga S, Ohtsubo M, Takihara Y, Kobayashi M. Ishikawa N, et al. Among authors: okada s. Blood Coagul Fibrinolysis. 2007 Jul;18(5):519-23. doi: 10.1097/MBC.0b013e328133f553. Blood Coagul Fibrinolysis. 2007. PMID: 17581330

6

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.

Shirao K, Okada S, Tajima G, Tsumura M, Hara K, Yasunaga S, Ohtsubo M, Hata I, Sakura N, Shigematsu Y, Takihara Y, Kobayashi M. Shirao K, et al. Among authors: okada s. Hum Genet. 2010 Jun;127(6):619-28. doi: 10.1007/s00439-010-0822-7. Epub 2010 Apr 8. Hum Genet. 2010. PMID: 20376488 Review.

7

[Hematological malignancies in congenital neutropenia].

Okada S, Nakamura K, Kobayashi M. Okada S, et al. Rinsho Ketsueki. 2010 Jul;51(7):553-8. Rinsho Ketsueki. 2010. PMID: 20693776 Review. Japanese. No abstract available.

8

Clinical and host genetic characteristics of Mendelian susceptibility to mycobacterial diseases in Japan.

Hoshina T, Takada H, Sasaki-Mihara Y, Kusuhara K, Ohshima K, Okada S, Kobayashi M, Ohara O, Hara T. Hoshina T, et al. Among authors: okada s. J Clin Immunol. 2011 Jun;31(3):309-14. doi: 10.1007/s10875-010-9498-y. Epub 2011 Jan 8. J Clin Immunol. 2011. PMID: 21221749

9

Decreased expression in nuclear factor-κB essential modulator due to a novel splice-site mutation causes X-linked ectodermal dysplasia with immunodeficiency.

Karakawa S, Okada S, Tsumura M, Mizoguchi Y, Ohno N, Yasunaga S, Ohtsubo M, Kawai T, Nishikomori R, Sakaguchi T, Takihara Y, Kobayashi M. Karakawa S, et al. Among authors: okada s. J Clin Immunol. 2011 Oct;31(5):762-72. doi: 10.1007/s10875-011-9560-4. Epub 2011 Jul 1. J Clin Immunol. 2011. PMID: 21720903

10

Disseminated BCG infection mimicking metastatic nasopharyngeal carcinoma in an immunodeficient child with a novel hypomorphic NEMO mutation.

Imamura M, Kawai T, Okada S, Izawa K, Takachi T, Iwabuchi H, Yoshida S, Hosokai R, Kanegane H, Yamamoto T, Umezu H, Nishikomori R, Heike T, Uchiyama M, Imai C. Imamura M, et al. Among authors: okada s. J Clin Immunol. 2011 Oct;31(5):802-10. doi: 10.1007/s10875-011-9568-9. Epub 2011 Jul 14. J Clin Immunol. 2011. PMID: 21755389

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