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

237 related items for PubMed ID: 24397858

  • 21. Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia.
    Stiburkova B, Ichida K, Sebesta I.
    Mol Genet Metab; 2011 Apr; 102(4):430-5. PubMed ID: 21256783
    [Abstract] [Full Text] [Related]

  • 22. New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions.
    Perdomo-Ramírez A, Ramos-Trujillo E, Claverie-Martín F, RenalTube Group.
    Genes (Basel); 2023 Sep 20; 14(9):. PubMed ID: 37761963
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Homozygous SLC2A9 mutations cause severe renal hypouricemia.
    Dinour D, Gray NK, Campbell S, Shu X, Sawyer L, Richardson W, Rechavi G, Amariglio N, Ganon L, Sela BA, Bahat H, Goldman M, Weissgarten J, Millar MR, Wright AF, Holtzman EJ.
    J Am Soc Nephrol; 2010 Jan 20; 21(1):64-72. PubMed ID: 19926891
    [Abstract] [Full Text] [Related]

  • 31. Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects.
    Zhou Z, Wang K, Zhou J, Wang C, Li X, Cui L, Han L, Liu Z, Ren W, Wang X, Zhang K, Li Z, Pan D, Li C, Shi Y.
    Mol Genet Genomic Med; 2019 Jul 20; 7(7):e00722. PubMed ID: 31131560
    [Abstract] [Full Text] [Related]

  • 32. Hypouricemia and hyperuricosuria in a pubescent girl: Answers.
    Stiburkova B, Sebesta I.
    Pediatr Nephrol; 2018 Dec 20; 33(12):2277-2279. PubMed ID: 29532232
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Rare case of nephrocalcinosis in the distal tubules caused by hereditary renal hypouricaemia 3 months after kidney transplantation.
    Okabayashi Y, Yamamoto I, Komatsuzaki Y, Niikura T, Yamakawa T, Katsumata H, Kawabe M, Katsuma A, Nakada Y, Kobayashi A, Koike Y, Miki J, Yamada H, Tanno Y, Ohkido I, Tsuboi N, Ichida K, Yamamoto H, Yokoo T.
    Nephrology (Carlton); 2016 Jul 20; 21 Suppl 1():67-71. PubMed ID: 26971588
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. 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 20; 37(4):1231-1234. PubMed ID: 38811494
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.