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163 results
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Ketone body metabolism and its defects.
Fukao T, Mitchell G, Sass JO, Hori T, Orii K, Aoyama Y. Fukao T, et al. Among authors: orii k. J Inherit Metab Dis. 2014 Jul;37(4):541-51. doi: 10.1007/s10545-014-9704-9. Epub 2014 Apr 8. J Inherit Metab Dis. 2014. PMID: 24706027 Review.
Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.
Orii KE, Fukao T, Song XQ, Mitchell GA, Kondo N. Orii KE, et al. Tohoku J Exp Med. 2008 Jul;215(3):227-36. doi: 10.1620/tjem.215.227. Tohoku J Exp Med. 2008. PMID: 18648183
Development of a newborn screening tool for mucopolysaccharidosis type I based on bivariate normal limits: Using glycosaminoglycan and alpha-L-iduronidase determinations on dried blood spots to predict symptoms.
Langan TJ, Jalal K, Barczykowski AL, Carter RL, Stapleton M, Orii K, Fukao T, Kobayashi H, Yamaguchi S, Tomatsu S. Langan TJ, et al. Among authors: orii k. JIMD Rep. 2020 Feb 10;52(1):35-42. doi: 10.1002/jmd2.12093. eCollection 2020 Mar. JIMD Rep. 2020. PMID: 32154058 Free PMC article.
Validation of Liquid Chromatography-Tandem Mass Spectrometry-Based 5-Plex Assay for Mucopolysaccharidoses.
Oguni T, Tomatsu S, Tanaka M, Orii K, Fukao T, Watanabe J, Fukuda S, Notsu Y, Vu DC, Can TBN, Nagai A, Yamaguchi S, Taketani T, Gelb MH, Kobayashi H. Oguni T, et al. Among authors: orii k. Int J Mol Sci. 2020 Mar 16;21(6):2025. doi: 10.3390/ijms21062025. Int J Mol Sci. 2020. PMID: 32188102 Free PMC article.
Newborn screening of mucopolysaccharidoses: past, present, and future.
Arunkumar N, Langan TJ, Stapleton M, Kubaski F, Mason RW, Singh R, Kobayashi H, Yamaguchi S, Suzuki Y, Orii K, Orii T, Fukao T, Tomatsu S. Arunkumar N, et al. Among authors: orii k. J Hum Genet. 2020 Jul;65(7):557-567. doi: 10.1038/s10038-020-0744-8. Epub 2020 Apr 10. J Hum Genet. 2020. PMID: 32277174
A complement factor B mutation in a large kindred with atypical hemolytic uremic syndrome.
Funato M, Uemura O, Ushijima K, Ohnishi H, Orii K, Kato Z, Yamakawa S, Nagai T, Ohara O, Kaneko H, Kondo N. Funato M, et al. Among authors: orii k. J Clin Immunol. 2014 Aug;34(6):691-5. doi: 10.1007/s10875-014-0058-8. Epub 2014 Jun 8. J Clin Immunol. 2014. PMID: 24906628
Immunodeficiency in Two Female Patients with Incontinentia Pigmenti with Heterozygous NEMO Mutation Diagnosed by LPS Unresponsiveness.
Ohnishi H, Kishimoto Y, Taguchi T, Kawamoto N, Nakama M, Kawai T, Nakayama M, Ohara O, Orii K, Fukao T. Ohnishi H, et al. Among authors: orii k. J Clin Immunol. 2017 Aug;37(6):529-538. doi: 10.1007/s10875-017-0417-3. Epub 2017 Jul 12. J Clin Immunol. 2017. PMID: 28702714
Total IgE at 6 months predicts remittance or persistence of atopic dermatitis at 14 months.
Kawamoto N, Fukao T, Kaneko H, Hirayama K, Sakurai S, Arai T, Kondo M, Kawamoto M, Matsui E, Orii K, Kasahara K, Takemura M, Seishima M, Shiraki M, Iwasa S, Kondo N. Kawamoto N, et al. Among authors: orii k. Allergy Asthma Proc. 2013 Jul-Aug;34(4):362-9. doi: 10.2500/aap.2013.34.3678. Allergy Asthma Proc. 2013. PMID: 23883601 Clinical Trial.
Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling.
Ohnishi H, Tochio H, Kato Z, Orii KE, Li A, Kimura T, Hiroaki H, Kondo N, Shirakawa M. Ohnishi H, et al. Proc Natl Acad Sci U S A. 2009 Jun 23;106(25):10260-5. doi: 10.1073/pnas.0812956106. Epub 2009 Jun 8. Proc Natl Acad Sci U S A. 2009. PMID: 19506249 Free PMC article.
Pediatric acute lymphoblastic leukemia mimicking Henoch-Schönlein purpura.
Funato M, Kaneko H, Kubota K, Ozeki M, Kanda K, Orii K, Kato Z, Fukao T, Kondo N. Funato M, et al. Among authors: orii k. Pediatr Int. 2011 Oct;53(5):766-768. doi: 10.1111/j.1442-200X.2011.03445.x. Pediatr Int. 2011. PMID: 21955011 No abstract available.
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