Maruo Y - Search Results

1

Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants.

Yanagi T, Nakahara S, Maruo Y. Yanagi T, et al. Among authors: maruo y. J Pediatr. 2017 Nov;190:159-162.e1. doi: 10.1016/j.jpeds.2017.07.014. Epub 2017 Sep 6. J Pediatr. 2017. PMID: 28888563

2

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

3

Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism.

Maruo Y, Nishizawa K, Sato H, Doida Y, Shimada M. Maruo Y, et al. Pediatrics. 1999 Jun;103(6 Pt 1):1224-7. doi: 10.1542/peds.103.6.1224. Pediatrics. 1999. PMID: 10353933

4

A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene.

Maruo Y, Wada S, Yamamoto K, Sato H, Yamano T, Shimada M. Maruo Y, et al. Eur J Pediatr. 1999 Jul;158(7):547-9. doi: 10.1007/s004310051143. Eur J Pediatr. 1999. PMID: 10412811

5

Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.

Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M. Maruo Y, et al. Pediatrics. 2000 Nov;106(5):E59. doi: 10.1542/peds.106.5.e59. Pediatrics. 2000. PMID: 11061796

6

Chemotherapy-induced unconjugated hyperbilirubinemia caused by a mutation of the bilirubin uridine-5'-diphosphate-glucuronosyltransferase gene.

Maruo Y, Sato H, Bamba N, Iwai M, Sawa H, Fujino H, Taga T, Ota S, Shimada M. Maruo Y, et al. J Pediatr Hematol Oncol. 2001 Jan;23(1):45-7. doi: 10.1097/00043426-200101000-00010. J Pediatr Hematol Oncol. 2001. PMID: 11196269

7

[UDP-glucuronosyltransferase].

Maruo Y, Sato H. Maruo Y, et al. Nihon Eiseigaku Zasshi. 2002 Jan;56(4):629-33. Nihon Eiseigaku Zasshi. 2002. PMID: 11868392 Review. Japanese.

8

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

9

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

10

Polymorphism of UDP-glucuronosyltransferase and drug metabolism.

Maruo Y, Iwai M, Mori A, Sato H, Takeuchi Y. Maruo Y, et al. Curr Drug Metab. 2005 Apr;6(2):91-9. doi: 10.2174/1389200053586064. Curr Drug Metab. 2005. PMID: 15853761 Review.

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