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Journal Abstract Search

147 related items for PubMed ID: 37360896

  • 1. Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I.
    Collazo Abal C, Romero Santos S, González Mao C, Pazos Lago EC, Barros Angueira F, Castiñeiras Ramos D.
    Adv Lab Med; 2021 Nov; 2(4):567-574. PubMed ID: 37360896
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  • 2. A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.
    Iguchi A, Sato T, Yamazaki M, Tasaki K, Suzuki Y, Iino N, Hasegawa H, Ichida K, Narita I.
    CEN Case Rep; 2016 Nov; 5(2):158-162. PubMed ID: 28508967
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  • 5. A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.
    Xu T, Xie X, Zhang Z, Zhao N, Deng Y, Li P.
    Clin Chim Acta; 2020 May; 504():168-171. PubMed ID: 32067994
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  • 6. XDH gene mutation is the underlying cause of classical xanthinuria: a second report.
    Levartovsky D, Lagziel A, Sperling O, Liberman U, Yaron M, Hosoya T, Ichida K, Peretz H.
    Kidney Int; 2000 Jun; 57(6):2215-20. PubMed ID: 10844591
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  • 7. Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II.
    Yamamoto T, Moriwaki Y, Takahashi S, Tsutsumi Z, Tuneyoshi K, Matsui K, Cheng J, Hada T.
    Metabolism; 2003 Nov; 52(11):1501-4. PubMed ID: 14624414
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  • 8. [Hereditary xanthinuria, rare cause of hypo-uric acidemia. 2 cases].
    Mayaudon H, Burnat P, Eulry F, Payen C, Dupuy O, Ducorps M, Bauduceau B.
    Presse Med; 1998 Apr 11; 27(14):661-3. PubMed ID: 9767921
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  • 9. Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease.
    Gonçalves PL, Diniz H, Tavares I, Dória S, Dong J, Kyriss M, Fairbanks L, Oliveira JP.
    Nephron; 2024 Apr 11; 148(8):578-583. PubMed ID: 38527446
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  • 10. Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase.
    Sekine M, Okamoto K, Ichida K.
    Biomedicines; 2021 Nov 20; 9(11):. PubMed ID: 34829959
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  • 11. [Xanthinuria type I as the cause of nephrolithiasis in 17-years old girl].
    Borucka B, Runowski D, Safranow K, Olszewska M, Jakubowska K, Chlubek D.
    Pol Merkur Lekarski; 2010 Aug 20; 29(170):111-4. PubMed ID: 20842824
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  • 14. Human xanthine dehydrogenase cDNA sequence and protein in an atypical case of type I xanthinuria in comparison with normal subjects.
    Yamamoto T, Moriwaki Y, Shibutani Y, Matsui K, Ueo T, Takahashi S, Tsutsumi Z, Hada T.
    Clin Chim Acta; 2001 Feb 20; 304(1-2):153-8. PubMed ID: 11165212
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  • 15. Purine disorders with hypouricemia.
    Sebesta I, Stiburkova B.
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2014 Feb 20; 35(1):87-92. PubMed ID: 24798598
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  • 16. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
    Stiburkova B, Pavelcova K, Petru L, Krijt J.
    Toxicol Appl Pharmacol; 2018 Aug 15; 353():102-108. PubMed ID: 29935280
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  • 17. Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
    Zhou Y, Zhang X, Ding R, Li Z, Hong Q, Wang Y, Zheng W, Geng X, Fan M, Cai G, Chen X, Wu D.
    Cell Physiol Biochem; 2015 Aug 15; 35(6):2412-21. PubMed ID: 25967871
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  • 18. Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I.
    Stiburkova B, Krijt J, Vyletal P, Bartl J, Gerhatova E, Korinek M, Sebesta I.
    Clin Chim Acta; 2012 Jan 18; 413(1-2):93-9. PubMed ID: 21963464
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  • 19. The lowest uric acid in kidney transplant and review of literature.
    Roozbeh J, Dehghani A, Haghpanah A, Malekmakan L.
    Int J Organ Transplant Med; 2022 Jan 18; 13(1):60-62. PubMed ID: 37383421
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  • 20. Xanthinuria type I: a rare cause of urolithiasis.
    Arikyants N, Sarkissian A, Hesse A, Eggermann T, Leumann E, Steinmann B.
    Pediatr Nephrol; 2007 Feb 18; 22(2):310-4. PubMed ID: 17115198
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