Toyota K - Search Results

1

Treatment with lactose (galactose)-restricted and medium-chain triglyceride-supplemented formula for neonatal intrahepatic cholestasis caused by citrin deficiency.

Hayasaka K, Numakura C, Toyota K, Kimura T. Hayasaka K, et al. Among authors: toyota k. JIMD Rep. 2012;2:37-44. doi: 10.1007/8904_2011_42. Epub 2011 Sep 6. JIMD Rep. 2012. PMID: 23430852 Free PMC article.

2

Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia.

Hayasaka K, Numakura C, Toyota K, Kakizaki S, Watanabe H, Haga H, Takahashi H, Takahashi Y, Kaneko M, Yamakawa M, Nunoi H, Kato T, Ueno Y, Mori M. Hayasaka K, et al. Among authors: toyota k. Mol Genet Metab Rep. 2014 Jan 14;1:42-50. doi: 10.1016/j.ymgmr.2013.12.002. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896073 Free PMC article.

3

An elderly Japanese patient with adult-onset type II citrullinemia with a novel D493G mutation in the SLC25A13 gene.

Takahashi Y, Koyama S, Tanaka H, Arawaka S, Wada M, Kawanami T, Haga H, Watanabe H, Toyota K, Numakura C, Hayasaka K, Kato T. Takahashi Y, et al. Among authors: toyota k. Intern Med. 2012;51(16):2131-4. doi: 10.2169/internalmedicine.51.7644. Epub 2012 Aug 15. Intern Med. 2012. PMID: 22892490 Free article.

4

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. Among authors: toyota k. 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

5

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.

Sato H, Uchida T, Toyota K, Kanno M, Hashimoto T, Watanabe M, Nakamura T, Tamiya G, Aoki K, Hayasaka K. Sato H, et al. Among authors: toyota k. J Hum Genet. 2013 Jan;58(1):7-10. doi: 10.1038/jhg.2012.116. Epub 2012 Sep 27. J Hum Genet. 2013. PMID: 23014115

6

A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy.

Toyota K, Hashimoto T, Ogino D, Matsunaga A, Ito M, Masakane I, Degawa N, Sato H, Shirai S, Umetsu K, Tamiya G, Saito T, Hayasaka K. Toyota K, et al. J Hum Genet. 2013 May;58(5):254-8. doi: 10.1038/jhg.2013.8. Epub 2013 Feb 14. J Hum Genet. 2013. PMID: 23407349

7

Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.

Sato H, Uchida T, Toyota K, Nakamura T, Tamiya G, Kanno M, Hashimoto T, Watanabe M, Aoki K, Hayasaka K. Sato H, et al. Among authors: toyota k. J Hum Genet. 2015 Jan;60(1):35-40. doi: 10.1038/jhg.2014.98. Epub 2014 Nov 13. J Hum Genet. 2015. PMID: 25391605

8

Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.

Ogino D, Hashimoto T, Hattori M, Sugawara N, Akioka Y, Tamiya G, Makino S, Toyota K, Mitsui T, Hayasaka K. Ogino D, et al. Among authors: toyota k. J Hum Genet. 2016 Feb;61(2):137-41. doi: 10.1038/jhg.2015.122. Epub 2015 Oct 15. J Hum Genet. 2016. PMID: 26467726

9

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

Toyota K, Ogino D, Hayashi M, Taki M, Saito K, Abe A, Hashimoto T, Umetsu K, Tsukaguchi H, Hayasaka K. Toyota K, et al. J Peripher Nerv Syst. 2013 Mar;18(1):97-8. doi: 10.1111/jns5.12014. J Peripher Nerv Syst. 2013. PMID: 23521651 No abstract available.

10

Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.

Ogino D, Hashimoto T, Hattori M, Sugawara N, Akioka Y, Tamiya G, Makino S, Toyota K, Mitsui T, Hayasaka K. Ogino D, et al. Among authors: toyota k. J Hum Genet. 2016 Aug;61(8):771-2. doi: 10.1038/jhg.2016.31. J Hum Genet. 2016. PMID: 27557799 No abstract available.

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