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URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia.
Claverie-Martin F, Trujillo-Suarez J, Gonzalez-Acosta H, Aparicio C, Justa Roldan ML, Stiburkova B, Ichida K, Martín-Gomez MA, Herrero Goñi M, Carrasco Hidalgo-Barquero M, Iñigo V, Enriquez R, Cordoba-Lanus E, Garcia-Nieto VM; RenalTube Group. Claverie-Martin F, et al. Among authors: stiburkova b. Clin Chim Acta. 2018 Jun;481:83-89. doi: 10.1016/j.cca.2018.02.030. Epub 2018 Feb 24. Clin Chim Acta. 2018. PMID: 29486147
Diagnostic tests for primary renal hypouricemia.
Sebesta I, Stiburkova B, Bartl J, Ichida K, Hosoyamada M, Taylor J, Marinaki A. Sebesta I, et al. Among authors: stiburkova b. Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1112-6. doi: 10.1080/15257770.2011.611483. Nucleosides Nucleotides Nucleic Acids. 2011. PMID: 22132965
Hereditary renal hypouricemia: a new role for allopurinol?
Bhasin B, Stiburkova B, De Castro-Pretelt M, Beck N, Bodurtha JN, Atta MG. Bhasin B, et al. Among authors: stiburkova b. Am J Med. 2014 Jan;127(1):e3-4. doi: 10.1016/j.amjmed.2013.08.025. Epub 2013 Nov 19. Am J Med. 2014. PMID: 24262806 No abstract available.
Purine disorders with hypouricemia.
Sebesta I, Stiburkova B. Sebesta I, et al. Among authors: stiburkova b. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014;35(1):87-92. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2014. PMID: 24798598
Complex analysis of urate transporters SLC2A9, SLC22A12 and functional characterization of non-synonymous allelic variants of GLUT9 in the Czech population: no evidence of effect on hyperuricemia and gout.
Hurba O, Mancikova A, Krylov V, Pavlikova M, Pavelka K, Stibůrková B. Hurba O, et al. Among authors: stiburkova b. PLoS One. 2014 Sep 30;9(9):e107902. doi: 10.1371/journal.pone.0107902. eCollection 2014. PLoS One. 2014. PMID: 25268603 Free PMC article.
69 results