Ueki I - Search Results

1

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: ueki i. Clin Endocrinol (Oxf). 2015 Mar;82(3):346-51. doi: 10.1111/cen.12596. Epub 2014 Oct 27. Clin Endocrinol (Oxf). 2015. PMID: 25154774

2

SRD5B1 gene analysis needed for the accurate diagnosis of primary 3-oxo-Delta4-steroid 5beta-reductase deficiency.

Ueki I, Kimura A, Chen HL, Yorifuji T, Mori J, Itoh S, Maruyama K, Ishige T, Takei H, Nittono H, Kurosawa T, Kage M, Matsuishi T. Ueki I, et al. J Gastroenterol Hepatol. 2009 May;24(5):776-85. doi: 10.1111/j.1440-1746.2008.05669.x. Epub 2008 Nov 3. J Gastroenterol Hepatol. 2009. PMID: 19175828

3

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: ueki i. Pediatr Res. 2010 Sep;68(3):258-63. doi: 10.1203/PDR.0b013e3181eb0188. Pediatr Res. 2010. PMID: 20531254

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: ueki i. 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

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: ueki i. Liver Transpl. 2011 Sep;17(9):1059-65. doi: 10.1002/lt.22331. Liver Transpl. 2011. PMID: 21567895 Free article.

6

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. 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.

7

Increased mitochondrial processing intermediates associated with three tRNA(Leu(UUR)) gene mutations.

Koga A, Koga Y, Akita Y, Fukiyama R, Ueki I, Yatsuga S, Matsuishi T. Koga A, et al. Among authors: ueki i. Neuromuscul Disord. 2003 Mar;13(3):259-62. doi: 10.1016/s0960-8966(02)00267-5. Neuromuscul Disord. 2003. PMID: 12609508

8

Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.

Ueki I, Koga Y, Povalko N, Akita Y, Nishioka J, Yatsuga S, Fukiyama R, Matsuishi T. Ueki I, et al. Mitochondrion. 2006 Feb;6(1):29-36. doi: 10.1016/j.mito.2005.10.003. Epub 2005 Dec 5. Mitochondrion. 2006. PMID: 16337222

9

Two neonates with intussusception accompanying severe hypoxia.

Ueki I, Nakashima E, Kumagai M, Kimura A, Hashimoto T. Ueki I, et al. Pediatr Int. 2005 Oct;47(5):595-7. doi: 10.1111/j.1442-200x.2005.02107.x. Pediatr Int. 2005. PMID: 16190974 No abstract available.

10

Intussusception in neonates: analysis of 14 Japanese patients.

Ueki I, Nakashima E, Kumagai M, Tananari Y, Kimura A, Fukuda S, Hashimoto T. Ueki I, et al. J Paediatr Child Health. 2004 Jul;40(7):388-91. doi: 10.1111/j.1440-1754.2004.00408.x. J Paediatr Child Health. 2004. PMID: 15228569

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

112 results

Search Page

Filters