Maruo Y - Search Results

1

Liver resection in patients with Gilbert's syndrome.

Arita J, Sugawara Y, Hashimoto T, Kaneko J, Kokudo N, Makuuchi M, Maruo Y. Arita J, et al. Among authors: maruo y. Surgery. 2003 Nov;134(5):835-7. doi: 10.1016/s0039-6060(03)00320-9. Surgery. 2003. PMID: 14639364 No abstract available.

2

Liver transplantation using donors with Gilbert syndrome.

Kaneko J, Sugawara Y, Maruo Y, Sato H, Tamura S, Imamura H, Kokudo N, Makuuchi M. Kaneko J, et al. Among authors: maruo y. Transplantation. 2006 Jul 27;82(2):282-5. doi: 10.1097/01.tp.0000226149.31117.e4. Transplantation. 2006. PMID: 16858293

3

Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

Aiso M, Yagi M, Tanaka A, Miura K, Miura R, Arizumi T, Takamori Y, Nakahara S, Maruo Y, Takikawa H. Aiso M, et al. Among authors: maruo y. Intern Med. 2017;56(6):661-664. doi: 10.2169/internalmedicine.56.7362. Epub 2017 Mar 17. Intern Med. 2017. PMID: 28321066 Free PMC article.

4

Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.

Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y. Takeuchi K, et al. Among authors: maruo y. J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8. doi: 10.1111/j.1440-1746.2004.03370.x. J Gastroenterol Hepatol. 2004. PMID: 15304120

5

Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.

Maruo Y, Sato H, Yamano T, Doida Y, Shimada M. Maruo Y, et al. J Pediatr. 1998 Jun;132(6):1045-7. doi: 10.1016/s0022-3476(98)70408-1. J Pediatr. 1998. PMID: 9627603

6

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.

Maruo Y, D'Addario C, Mori A, Iwai M, Takahashi H, Sato H, Takeuchi Y. Maruo Y, et al. Hum Genet. 2004 Nov;115(6):525-6. doi: 10.1007/s00439-004-1183-x. Epub 2004 Sep 17. Hum Genet. 2004. PMID: 15378351

7

Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome.

Sugita K, Maruo Y, Kurosawa H, Tsuchioka A, Fujiwara T, Mori A, Ideguchi H, Eguchi M. Sugita K, et al. Among authors: maruo y. Pediatr Int. 2007 Aug;49(4):540-2. doi: 10.1111/j.1442-200X.2007.02410.x. Pediatr Int. 2007. PMID: 17587286 No abstract available.

8

Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.

Matsui K, Maruo Y, Sato H, Takeuchi Y. Matsui K, et al. Among authors: maruo y. BMC Gastroenterol. 2010 Jun 8;10:57. doi: 10.1186/1471-230X-10-57. BMC Gastroenterol. 2010. PMID: 20529348 Free PMC article.

9

Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.

Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y. Maruo Y, et al. J Gastroenterol Hepatol. 2016 Feb;31(2):403-8. doi: 10.1111/jgh.13071. J Gastroenterol Hepatol. 2016. PMID: 26250421

10

Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.

Maruo Y, Poon KK, Ito M, Iwai M, Takahashi H, Mori A, Sato H, Takeuchi Y. Maruo Y, et al. Clin Genet. 2003 Nov;64(5):420-3. doi: 10.1034/j.1399-0004.2003.00136.x. Clin Genet. 2003. PMID: 14616765

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