2020
DOI: 10.1016/j.revmed.2020.02.014
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La maladie goutteuse

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Cited by 29 publications
(20 citation statements)
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References 53 publications
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“…Serum UA level is regulated by UA transport proteins in the kidney and intestine, specifically GLUT9 (SLC2A9), URAT1 (SLC22A12), and ABCG2 (Scuiller et al, 2020). GLUT9, encoded by the SLC2A9 gene, is an important proximal tubular transporter protein for UA and plays a key role in hyperuricemia.…”
Section: Discussionmentioning
confidence: 99%
“…Serum UA level is regulated by UA transport proteins in the kidney and intestine, specifically GLUT9 (SLC2A9), URAT1 (SLC22A12), and ABCG2 (Scuiller et al, 2020). GLUT9, encoded by the SLC2A9 gene, is an important proximal tubular transporter protein for UA and plays a key role in hyperuricemia.…”
Section: Discussionmentioning
confidence: 99%
“…Gout is a metabolic disease, caused by elevation of serum urate level (Scuiller et al, 2020). The prevalence of gout in the world ranges from 0.68%-3.90% and is still increasing steadily (Dalbeth et al, 2021).…”
Section: Introductionmentioning
confidence: 99%
“…Real-life observational data show that the majority of patients do not reach targeted SU levels and still experience recurrent flares [ 6 , 9 , 10 ]. Under-prescription of ULT, poor treatment compliance, and fears and beliefs often insufficiently addressed in patient education have been identified as the main barriers for optimal care [ 11 ].…”
Section: Introductionmentioning
confidence: 99%