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Journal Abstract Search

258 related items for PubMed ID: 26389017

  • 1. Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.
    Anglani F, D'Angelo A, Bertizzolo LM, Tosetto E, Ceol M, Cremasco D, Bonfante L, Addis MA, Del Prete D, Dent Disease Italian Network.
    Springerplus; 2015; 4():492. PubMed ID: 26389017
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  • 2.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lieske JC, Milliner DS, Beara-Lasic L, Harris P, Cogal A, Abrash E.
    ; 1993. PubMed ID: 22876375
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  • 9. Dent disease: A window into calcium and phosphate transport.
    Anglani F, Gianesello L, Beara-Lasic L, Lieske J.
    J Cell Mol Med; 2019 Nov; 23(11):7132-7142. PubMed ID: 31472005
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  • 14. Dent's disease: clinical features and molecular basis.
    Claverie-Martín F, Ramos-Trujillo E, García-Nieto V.
    Pediatr Nephrol; 2011 May; 26(5):693-704. PubMed ID: 20936522
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  • 16. Dent disease in children: diagnostic and therapeutic considerations.
    Szczepanska M, Zaniew M, Recker F, Mizerska-Wasiak M, Zaluska-Lesniewska I, Kilis-Pstrusinska K, Adamczyk P, Zawadzki J, Pawlaczyk K, Ludwig M, Sikora P.
    Clin Nephrol; 2015 Oct; 84(4):222-30. PubMed ID: 26308078
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  • 17. 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
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  • 18. A Novel CLCN5 Splice Site Mutation in a Boy with Incomplete Phenotype of Dent Disease.
    Bitsori M, Vergadi E, Galanakis E.
    J Pediatr Genet; 2019 Dec; 8(4):235-239. PubMed ID: 31687264
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  • 19. Dent disease manifesting as nephrotic syndrome.
    Chen Q, Li Y, Wu X.
    Intractable Rare Dis Res; 2023 Feb; 12(1):67-70. PubMed ID: 36873671
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