Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia-Reference-Cited by-同舟云学术

Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia

Published:2017 Issue:6 Volume:56 Page:661-664
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Aiso Mitsuhiko¹,Yagi Minami¹,Tanaka Atsushi¹,Miura Kotaro¹,Miura Ryo¹,Arizumi Toshihiko¹,Takamori Yoriyuki¹,Nakahara Sayuri²,Maruo Yoshihiro²,Takikawa Hajime¹

Affiliation:

1. Department of Medicine, Teikyo University School of Medicine, Japan

2. Department of Pediatrics, Shiga University of Medical Science, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/56/6/56_56.7362/_pdf

Reference14 articles.

1. 1. Maruo Y, Ohta S. Gilbert syndrome and blood diseases. Jpn J Pediatr Hematol 18: 601-608, 2004.

2. 2. Bosma PJ, Chowdhury JR, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 333: 1171-1175, 1995.

3. 3. Usuki K. Hemolytic anemia;Diagnosis and treatment. Nihon Naika Gakkai Zasshi 104: 1389-1396, 2015 (in Japanese).

4. 4. Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert's syndrome. Lancet 347: 557-558, 1996.

5. 5. Maruo Y, D'Addario C, Mori A, et al. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Hum Genet 115: 525-526, 2004.

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