These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

213 related items for PubMed ID: 22045201

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 Nov 26; 38(4):316-20. PubMed ID: 24107611
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia.
    Li Z, Ding H, Chen C, Chen Y, Wang DW, Lv Y.
    Gene; 2013 Jan 01; 512(1):97-101. PubMed ID: 23043931
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.
    Sekiya M, Matsuda T, Yamamoto Y, Furuta Y, Ohyama M, Murayama Y, Sugano Y, Ohsaki Y, Iwasaki H, Yahagi N, Yatoh S, Suzuki H, Shimano H.
    BMC Med Genet; 2020 May 06; 21(1):91. PubMed ID: 32375679
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia.
    Sugihara S, Hisatome I, Kuwabara M, Niwa K, Maharani N, Kato M, Ogino K, Hamada T, Ninomiya H, Higashi Y, Ichida K, Yamamoto K.
    Circ J; 2015 May 06; 79(5):1125-32. PubMed ID: 25739858
    [Abstract] [Full Text] [Related]

  • 16. 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.
    Clin Chim Acta; 2018 Jun 06; 481():83-89. PubMed ID: 29486147
    [Abstract] [Full Text] [Related]

  • 17. Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease.
    Stiburkova B, Stekrova J, Nakamura M, Ichida K.
    Am J Med Sci; 2015 Oct 06; 350(4):268-71. PubMed ID: 26418379
    [Abstract] [Full Text] [Related]

  • 18. URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews.
    Dinour D, Bahn A, Ganon L, Ron R, Geifman-Holtzman O, Knecht A, Gafter U, Rachamimov R, Sela BA, Burckhardt G, Holtzman EJ.
    Nephrol Dial Transplant; 2011 Jul 06; 26(7):2175-81. PubMed ID: 21148271
    [Abstract] [Full Text] [Related]

  • 19. Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
    Mancikova A, Krylov V, Hurba O, Sebesta I, Nakamura M, Ichida K, Stiburkova B.
    Clin Exp Nephrol; 2016 Aug 06; 20(4):578-584. PubMed ID: 26500098
    [Abstract] [Full Text] [Related]

  • 20. Biochemical characterization of renal hypouricemia-associated mutations in urate transporter genes using human cells.
    Toyoda Y, Takada T, Nakayama A, Shinomiya N, Matsuo H.
    Hum Cell; 2024 Jul 06; 37(4):1231-1234. PubMed ID: 38811494
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.