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Journal Abstract Search

157 related items for PubMed ID: 17445045

  • 1. Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.
    Ohtsuka Y, Zaitsu M, Ichida K, Isomura N, Tsuji K, Sato T, Hamasaki Y.
    Pediatr Int; 2007 Apr; 49(2):235-7. PubMed ID: 17445045
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  • 2. Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury.
    Kaito H, Ishimori S, Nozu K, Shima Y, Nakanishi K, Yoshikawa N, Iijima K.
    Am J Nephrol; 2013 Apr; 38(4):316-20. PubMed ID: 24107611
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  • 6. Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report.
    Furuto Y, Kawamura M, Namikawa A, Takahashi H, Shibuya Y, Mori T, Sohara E.
    BMC Nephrol; 2019 Nov 26; 20(1):433. PubMed ID: 31771519
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  • 7. Hypouricemia and hyperuricosuria in a pubescent girl: Answers.
    Stiburkova B, Sebesta I.
    Pediatr Nephrol; 2018 Dec 26; 33(12):2277-2279. PubMed ID: 29532232
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  • 9. Acute renal failure after exercise in a Japanese sumo wrestler with renal hypouricemia.
    Mima A, Ichida K, Matsubara T, Kanamori H, Inui E, Tanaka M, Manabe Y, Iehara N, Tanaka Y, Yanagita M, Yoshioka A, Arai H, Kawamura M, Usami K, Hosoya T, Kita T, Fukatsu A.
    Am J Med Sci; 2008 Dec 26; 336(6):512-4. PubMed ID: 19092327
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  • 11. Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.
    Stiburkova B, Sebesta I, Ichida K, Nakamura M, Hulkova H, Krylov V, Kryspinova L, Jahnova H.
    Eur J Hum Genet; 2013 Oct 26; 21(10):1067-73. PubMed ID: 23386035
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  • 15. [Water electrolyte imbalance associated with kidney tubular transport inborn error].
    Igarashi T.
    Nihon Naika Gakkai Zasshi; 2003 May 10; 92(5):818-25. PubMed ID: 12808907
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  • 16. The Case | A 33-year-old woman with gross hematuria.
    Choi HS, Kim SS, Choi HI, Song JH, Kim CS, Bae EH, Ma SK, Kim SW.
    Kidney Int; 2018 Oct 10; 94(4):837-838. PubMed ID: 30243328
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  • 20. Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families.
    Kawamura Y, Toyoda Y, Ohnishi T, Hisatomi R, Higashino T, Nakayama A, Shimizu S, Yanagi M, Kamimaki I, Fujimaru R, Suzuki H, Shinomiya N, Takada T, Matsuo H.
    Rheumatology (Oxford); 2020 Dec 01; 59(12):3988-3990. PubMed ID: 33011794
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