First clinical practice guideline for renal hypouricaemia: a rare disorder that aided the development of urate-lowering drugs for gout-Reference-Cited by-同舟云学术

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First clinical practice guideline for renal hypouricaemia: a rare disorder that aided the development of urate-lowering drugs for gout

Published:2021-03-31 Issue:9 Volume:60 Page:3961-3963
ISSN:1462-0324
Container-title:Rheumatology
language:en
Short-container-title:

Author:

Nakayama Akiyoshi¹^ORCID,Matsuo Hirotaka¹,Abhishek Abhishek²,Ichida Kimiyoshi³,Shinomiya Nariyoshi¹^ORCID,

Affiliation:

1. Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan

2. Academic Rheumatology, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, UK

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

Funder

Ministry of Health, Labour and Welfare of Japan

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Link

http://academic.oup.com/rheumatology/advance-article-pdf/doi/10.1093/rheumatology/keab322/37951181/keab322.pdf

Reference10 articles.

1. Clinical practice guideline for renal hypouricemia (1st edition);Nakayama;Hum Cell,2019

2. Molecular identification of a renal urate anion exchanger that regulates blood urate levels;Enomoto;Nature,2002

3. Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion;Ichida;J Am Soc Nephrol,2004

4. Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia;Matsuo;Am J Hum Genet,2008

5. Homozygous SLC2A9 mutations cause severe renal hypouricemia;Dinour;J Am Soc Nephrol,2010

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1. Uric Acid Metabolism, Uric Acid Transporters and Dysuricemia;YAKUGAKU ZASSHI;2024-06-01

2. Biochemical characterization of renal hypouricemia-associated mutations in urate transporter genes using human cells;Human Cell;2024-05-29

3. Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9;Neuromuscular Disorders;2024-01

4. Dysuricemia;Biomedicines;2023-11-28

5. New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions;Genes;2023-09-20

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