Nishimura A - 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. 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

Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study.

Miyamoto S, Umeda K, Kurata M, Nishimura A, Yanagimachi M, Ishimura M, Sato M, Shigemura T, Kato M, Sasahara Y, Iguchi A, Koike T, Takahashi Y, Kajiwara M, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T. Miyamoto S, et al. Among authors: nishimura a. J Clin Immunol. 2021 Nov;41(8):1865-1877. doi: 10.1007/s10875-021-01112-5. Epub 2021 Aug 27. J Clin Immunol. 2021. PMID: 34448087 Free PMC article.

3

Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.

Okano T, Nishimura A, Inoue K, Naruto T, Tokoro S, Tomoda T, Kamiya T, Simbo A, Akutsu Y, Okamoto K, Yeh T, Isoda T, Yanagimachi M, Kajiwara M, Imai K, Kanegane H, Mori M, Morio T, Takagi M. Okano T, et al. Among authors: nishimura a. Rheumatology (Oxford). 2021 Dec 1;60(12):e429-e431. doi: 10.1093/rheumatology/keab513. Rheumatology (Oxford). 2021. PMID: 34528076 No abstract available.

4

PAX3/7-FOXO1 fusion-negative alveolar rhabdomyosarcoma in Schuurs-Hoeijmakers syndrome.

Ohkawa T, Nishimura A, Kosaki K, Aoki-Nogami Y, Tomizawa D, Kashimada K, Morio T, Kato M, Mizutani S, Takagi M. Ohkawa T, et al. Among authors: nishimura a. J Hum Genet. 2022 Jan;67(1):51-54. doi: 10.1038/s10038-021-00965-3. Epub 2021 Aug 2. J Hum Genet. 2022. PMID: 34341476

5

Exonic deletion of CASP10 in a patient presenting with systemic juvenile idiopathic arthritis, but not with autoimmune lymphoproliferative syndrome type IIa.

Tadaki H, Saitsu H, Kanegane H, Miyake N, Imagawa T, Kikuchi M, Hara R, Kaneko U, Kishi T, Miyamae T, Nishimura A, Doi H, Tsurusaki Y, Sakai H, Yokota S, Matsumoto N. Tadaki H, et al. Among authors: nishimura a. Int J Immunogenet. 2011 Aug;38(4):287-93. doi: 10.1111/j.1744-313X.2011.01005.x. Epub 2011 Mar 7. Int J Immunogenet. 2011. PMID: 21382177

6

Isolation of temperature-sensitive aminoacyl-tRNA synthetase mutants from an Escherichia coli strain harboring the pemK plasmid.

Masuda Y, Tsuchimoto S, Nishimura A, Ohtsubo E. Masuda Y, et al. Among authors: nishimura a. Mol Gen Genet. 1993 Apr;238(1-2):169-76. doi: 10.1007/BF00279544. Mol Gen Genet. 1993. PMID: 8479423

7

Paternal somatic mosaicism of a TGFBR2 mutation transmitting to an affected son with Loeys-Dietz syndrome.

Watanabe Y, Sakai H, Nishimura A, Miyake N, Saitsu H, Mizuguchi T, Matsumoto N. Watanabe Y, et al. Among authors: nishimura a. Am J Med Genet A. 2008 Dec 1;146A(23):3070-4. doi: 10.1002/ajmg.a.32567. Am J Med Genet A. 2008. PMID: 19006214

8

Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants.

Tozawa T, Nishimura A, Ueno T, Shikata A, Taura Y, Yoshida T, Nakagawa N, Wada T, Kosugi S, Uehara T, Takenouchi T, Kosaki K, Chiyonobu T. Tozawa T, et al. Among authors: nishimura a. Hum Genome Var. 2021 Jan 26;8(1):4. doi: 10.1038/s41439-021-00136-y. Hum Genome Var. 2021. PMID: 33500398 Free PMC article.

9

Development of corpus callosum in preterm infants is affected by the prematurity: in vivo assessment of diffusion tensor imaging at term-equivalent age.

Hasegawa T, Yamada K, Morimoto M, Morioka S, Tozawa T, Isoda K, Murakami A, Chiyonobu T, Tokuda S, Nishimura A, Nishimura T, Hosoi H. Hasegawa T, et al. Among authors: nishimura a, nishimura t. Pediatr Res. 2011 Mar;69(3):249-54. doi: 10.1203/PDR.0b013e3182084e54. Pediatr Res. 2011. PMID: 21131895

10

Treatment for Leigh syndrome by monitoring dichloroacetate concentration.

Katsumi Y, Morimoto M, Nishimura A, Naito E, Sugimoto T. Katsumi Y, et al. Among authors: nishimura a. Pediatr Int. 2009 Apr;51(2):293-5. doi: 10.1111/j.1442-200X.2009.02815.x. Pediatr Int. 2009. PMID: 19379261 No abstract available.

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