Nittono H - Search Results

1

Liver disease in infancy caused by oxysterol 7 α-hydroxylase deficiency: successful treatment with chenodeoxycholic acid.

Dai D, Mills PB, Footitt E, Gissen P, McClean P, Stahlschmidt J, Coupry I, Lavie J, Mochel F, Goizet C, Mizuochi T, Kimura A, Nittono H, Schwarz K, Crick PJ, Wang Y, Griffiths WJ, Clayton PT. Dai D, et al. Among authors: nittono h. J Inherit Metab Dis. 2014 Sep;37(5):851-61. doi: 10.1007/s10545-014-9695-6. J Inherit Metab Dis. 2014. PMID: 24658845

2

Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.

Seki Y, Mizuochi T, Kimura A, Takahashi T, Ohtake A, Hayashi S, Morimura T, Ohno Y, Hoshina T, Ihara K, Takei H, Nittono H, Kurosawa T, Homma K, Hasegawa T, Matsuishi T. Seki Y, et al. Among authors: nittono h. J Inherit Metab Dis. 2013 May;36(3):565-73. doi: 10.1007/s10545-012-9526-6. Epub 2012 Nov 16. J Inherit Metab Dis. 2013. PMID: 23160874

3

Successful heterozygous living donor liver transplantation for an oxysterol 7α-hydroxylase deficiency in a Japanese patient.

Mizuochi T, Kimura A, Suzuki M, Ueki I, Takei H, Nittono H, Kakiuchi T, Shigeta T, Sakamoto S, Fukuda A, Nakazawa A, Shimizu T, Kurosawa T, Kasahara M. Mizuochi T, et al. Among authors: nittono h. Liver Transpl. 2011 Sep;17(9):1059-65. doi: 10.1002/lt.22331. Liver Transpl. 2011. PMID: 21567895 Free article.

4

Neonatal cholestasis with increased 3β-monohydroxy-Δ⁵ bile acids in serum and urine: not necessarily primary oxysterol 7α hydroxylase deficiency.

Kimura A, Nittono H, Mizuochi T, Ueki I, Kurosawa T, Muto A, Takei H. Kimura A, et al. Among authors: nittono h. Clin Chim Acta. 2012 Oct 9;413(19-20):1700-4. doi: 10.1016/j.cca.2012.05.016. Epub 2012 May 28. Clin Chim Acta. 2012. PMID: 22652365

5

Complete Recovery of Oxysterol 7α-Hydroxylase Deficiency by Living Donor Transplantation in a 4-Month-Old Infant: the First Korean Case Report and Literature Review.

Hong J, Oh SH, Yoo HW, Nittono H, Kimura A, Kim KM. Hong J, et al. Among authors: nittono h. J Korean Med Sci. 2018 Nov 22;33(51):e324. doi: 10.3346/jkms.2018.33.e324. eCollection 2018 Dec 17. J Korean Med Sci. 2018. PMID: 30546280 Free PMC article.

6

Bile Acid Synthesis Disorders in Japan: Long-Term Outcome and Chenodeoxycholic Acid Treatment.

Kimura A, Mizuochi T, Takei H, Ohtake A, Mori J, Shinoda K, Hashimoto T, Kasahara M, Togawa T, Murai T, Iida T, Nittono H. Kimura A, et al. Among authors: nittono h. Dig Dis Sci. 2021 Nov;66(11):3885-3892. doi: 10.1007/s10620-020-06722-4. Epub 2021 Jan 1. Dig Dis Sci. 2021. PMID: 33385262

7

Molecular genetic and bile acid profiles in two Japanese patients with 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficiency.

Mizuochi T, Kimura A, Ueki I, Takahashi T, Hashimoto T, Takao A, Seki Y, Takei H, Nittono H, Kurosawa T, Matsuishi T. Mizuochi T, et al. Among authors: nittono h. Pediatr Res. 2010 Sep;68(3):258-63. doi: 10.1203/PDR.0b013e3181eb0188. Pediatr Res. 2010. PMID: 20531254

8

Distinguishing primary from secondary Δ(4) -3-oxosteroid 5β-reductase (SRD5B1, AKR1D1) deficiency by urinary steroid analysis.

Yanagi T, Mizuochi T, Homma K, Ueki I, Seki Y, Hasegawa T, Takei H, Nittono H, Kurosawa T, Matsuishi T, Kimura A. Yanagi T, et al. Among authors: nittono h. Clin Endocrinol (Oxf). 2015 Mar;82(3):346-51. doi: 10.1111/cen.12596. Epub 2014 Oct 27. Clin Endocrinol (Oxf). 2015. PMID: 25154774

9

Cholestenoic acids regulate motor neuron survival via liver X receptors.

Theofilopoulos S, Griffiths WJ, Crick PJ, Yang S, Meljon A, Ogundare M, Kitambi SS, Lockhart A, Tuschl K, Clayton PT, Morris AA, Martinez A, Reddy MA, Martinuzzi A, Bassi MT, Honda A, Mizuochi T, Kimura A, Nittono H, De Michele G, Carbone R, Criscuolo C, Yau JL, Seckl JR, Schüle R, Schöls L, Sailer AW, Kuhle J, Fraidakis MJ, Gustafsson JÅ, Steffensen KR, Björkhem I, Ernfors P, Sjövall J, Arenas E, Wang Y. Theofilopoulos S, et al. Among authors: nittono h. J Clin Invest. 2014 Nov;124(11):4829-42. doi: 10.1172/JCI68506. Epub 2014 Oct 1. J Clin Invest. 2014. PMID: 25271621 Free PMC article.

10

Neonatal cholestatic liver disease in an Asian patient with a homozygous mutation in the oxysterol 7alpha-hydroxylase gene.

Ueki I, Kimura A, Nishiyori A, Chen HL, Takei H, Nittono H, Kurosawa T. Ueki I, et al. Among authors: nittono h. J Pediatr Gastroenterol Nutr. 2008 Apr;46(4):465-9. doi: 10.1097/MPG.0b013e31815a9911. J Pediatr Gastroenterol Nutr. 2008. PMID: 18367963 No abstract available.

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