Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function-Reference-Cited by-同舟云学术

Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function

Published:2022-05-01 Issue:9 Volume:61 Page:1383-1386
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Miyazaki Satoshi¹,Hamada Toshihiro²,Sugihara Shinobu³,Mizuta Einosuke⁴,Endo Yusuke⁵,Ohtahara Akira⁴,Komatsu Koji⁶,Kuwabara Masanari⁷,Fukuuchi Tomoko⁸,Kaneko Kiyoko⁹,Ichida Kimiyoshi¹⁰,Ogino Kazuhide¹¹,Ninomiya Haruaki¹²,Yamamoto Kazuhiro¹³,Nakamura Takashi¹⁴,Hisatome Ichiro¹⁵

Affiliation:

1. Division of Cardiology, Fujii Masao Memorial Hospital, Japan

2. Department of Community-Based Family Medicine, Tottori University, Faculty of Medicine, Japan

3. Health Service Center, Shimane University, Japan

4. Department of Cardiology, San-in Rosai Hospital, Japan

5. Advanced Medicine, Innovation and Clinical Research Center, Tottori University Hospital, Japan

6. Department of Psychiatry Disease, Tottori University, Japan

7. Department of Cardiology, Toranomon Hospital, Japan

8. Laboratory of Biomedical and Analytical Sciences, Faculty of Pharma-Science, Teikyo University, Japan

9. Faculty of Pharmaceutical Sciences, Teikyo Heisei University, Japan

10. Department of Pathophysiology, Tokyo University of Pharmacy and Life Sciences, Japan

11. Department of Cardiology, Japanese Red Cross Tottori Hospital, Japan

12. Department of Biological Regulation, Tottori University Faculty of Medicine, Japan

13. Division of Cardiovascular Medicine, Department of Molecular Medicine and Therapeutics, Faculty of Medicine, Tottori University, Japan

14. Sanwa Kagaku Kenkyusho, Japan

15. Department of Cardiovascular Medicine, Yonago Medical Center, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/61/9/61_7897-21/_pdf

Reference23 articles.

1. 1. Nakayama A, Matsuo H, Ohtahara A, et al. Clinical practice guideline for renal hypouricemia (1st edition). Hum Cell 32: 83-87, 2019.

2. 2. Ogino K, Hisatome I, Saitoh M, et al. Clinical significance of hypouricemia in hospitalized patients. J Med 22: 76-82, 1991.

3. 3. Hisatome I, Ogino K, Kotake H, et al. Cause of persistent hypouricemia in outpatients. Nephron 51: 13-16, 1989.

4. 4. Kojima T, Nishina T, Kitamura M, Hosoya T, Nishioka K. Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria. Clin Chim Acta 137: 189-198, 1984.

5. 5. Enomoto A, Kimura H, Chairoungdua A, et al. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 417: 447-452, 2002.

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impact of Hyper- and Hypo-Uricemia on Kidney Function;Biomedicines;2023-04-24

2. Candidate causative variant for xanthinuria in a Domestic Shorthair cat;Animal Genetics;2023-03-27