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

Journal Abstract Search


184 related items for PubMed ID: 7753256

  • 1. Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: is the disease identical to Dent's disease in United Kingdom?
    Igarashi T, Hayakawa H, Shiraga H, Kawato H, Yan K, Kawaguchi H, Yamanaka T, Tsuchida S, Akagi K.
    Nephron; 1995; 69(3):242-7. PubMed ID: 7753256
    [Abstract] [Full Text] [Related]

  • 2. Dent's disease--the hypercalciuric variant of Fanconi's syndrome.
    Kabícek P, Bayer M.
    Sb Lek; 1998; 99(1):21-4. PubMed ID: 9748795
    [Abstract] [Full Text] [Related]

  • 3. Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance.
    Wrong OM, Norden AG, Feest TG.
    QJM; 1994 Aug; 87(8):473-93. PubMed ID: 7922301
    [Abstract] [Full Text] [Related]

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

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

  • 6. Phenotype and genotype of Dent's disease in three Chinese boys.
    Li P, Huang JP.
    Nephrology (Carlton); 2009 Apr; 14(2):139-42. PubMed ID: 19076289
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease.
    Igarashi T, Inatomi J, Ohara T, Kuwahara T, Shimadzu M, Thakker RV.
    Kidney Int; 2000 Aug; 58(2):520-7. PubMed ID: 10916075
    [Abstract] [Full Text] [Related]

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

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 12. Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
    Akuta N, Lloyd SE, Igarashi T, Shiraga H, Matsuyama T, Yokoro S, Cox JP, Thakker RV.
    Kidney Int; 1997 Oct; 52(4):911-6. PubMed ID: 9328929
    [Abstract] [Full Text] [Related]

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

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

  • 15. Evidence for genetic heterogeneity in Dent's disease.
    Hoopes RR, Raja KM, Koich A, Hueber P, Reid R, Knohl SJ, Scheinman SJ.
    Kidney Int; 2004 May; 65(5):1615-20. PubMed ID: 15086899
    [Abstract] [Full Text] [Related]

  • 16. Molecular analysis of the CLCN5 gene in Dent's disease: first mutation identified in a patient from South America.
    Ramos-Trujillo E, Garcia-Nieto V, Gonzalez-Acosta H, Vara J, Pérez-Diaz V, Nadal I, Oliveros R, Claverie-Martin F.
    Clin Nephrol; 2007 Dec; 68(6):367-72. PubMed ID: 18184518
    [Abstract] [Full Text] [Related]

  • 17. Chloride channels and endocytosis: new insights from Dent's disease and ClC-5 knockout mice.
    Devuyst O, Jouret F, Auzanneau C, Courtoy PJ.
    Nephron Physiol; 2005 Dec; 99(3):p69-73. PubMed ID: 15637424
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Hypercalciuria and nephrocalcinosis in the oculocerebrorenal syndrome.
    Sliman GA, Winters WD, Shaw DW, Avner ED.
    J Urol; 1995 Apr; 153(4):1244-6. PubMed ID: 7869519
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 10.