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Journal Abstract Search

279 related items for PubMed ID: 32533415

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  • 5. A novel CLCN5 mutation in a Chinese boy with Dent's disease.
    Ji LN, Chen CY, Wang JJ, Cao L.
    World J Pediatr; 2014 Aug; 10(3):275-7. PubMed ID: 25124980
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  • 6. [Clinical and genetic analysis of Dent' s disease in 6 Chinese children with low molecular weight proteinuria].
    Zhu BZ, Li P, Huang JP.
    Zhonghua Er Ke Za Zhi; 2010 May; 48(5):329-33. PubMed ID: 20654030
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  • 7. Clinical and genetic characteristics of Dent's disease type 1 in Europe.
    Burballa C, Cantero-Recasens G, Prikhodina L, Lugani F, Schlingmann K, Ananin PV, Besouw M, Bockenhauer D, Madariaga L, Bertholet-Thomas A, Taroni F, Parolin M, Conlon P, Emma F, Del Prete D, Chauveau D, Koster-Kamphuis L, Fila M, Pasini A, Castro I, Colussi G, Gil M, Mohidin B, Wlodkowski T, Schaefer F, Ariceta G, DENT study group.
    Nephrol Dial Transplant; 2023 May 31; 38(6):1497-1507. PubMed ID: 36441012
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  • 8. [Clinical features and genetic variants of Dent disease in 10 children].
    Zhao SL, Zhao F, Sha YG, Chen QX, Cheng XQ, Huang SM.
    Zhonghua Er Ke Za Zhi; 2018 Apr 02; 56(4):289-293. PubMed ID: 29614570
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  • 9. Dent's disease complicated by an acute Budd-Chiari syndrome.
    Platt C, Jadresic L, Dudley J, Hartley JL.
    BMJ Case Rep; 2014 Jan 07; 2014():. PubMed ID: 24398869
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  • 14. A novel likely pathogenic CLCN5 variant in Dent's disease.
    Hayward S, Norton J, Bownass L, Platt C, Genomics England Research Consortium, Campbell H, Watson E, Forrester N, Smithson S, Menon A.
    BMC Nephrol; 2023 Aug 28; 24(1):256. PubMed ID: 37641036
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  • 15. Dent's disease.
    Devuyst O, Thakker RV.
    Orphanet J Rare Dis; 2010 Oct 14; 5():28. PubMed ID: 20946626
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  • 16. Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.
    Tanuma A, Sato H, Takeda T, Hosojima M, Obayashi H, Hama H, Iino N, Hosaka K, Kaseda R, Imai N, Ueno M, Yamazaki M, Sakimura K, Gejyo F, Saito A.
    Nephron Physiol; 2007 Oct 14; 107(4):p87-97. PubMed ID: 18025833
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  • 17. Genetic Analysis of Dent's Disease and Functional Research of CLCN5 Mutations.
    Zhang Y, Fang X, Xu H, Shen Q.
    DNA Cell Biol; 2017 Dec 14; 36(12):1151-1158. PubMed ID: 29058463
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  • 18. Proteinuria in Dent disease: a review of the literature.
    van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A.
    Pediatr Nephrol; 2017 Oct 14; 32(10):1851-1859. PubMed ID: 27757584
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  • 19. A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations.
    Mollataheri A, Mojbafan M, Hosseini R, Houman N, Mousavi M, Otoukesh H.
    Nephron; 2023 Oct 14; 147(8):470-477. PubMed ID: 36646056
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  • 20. Chloride channels and endocytosis: new insights from Dent's disease and CLC-5 knockout mice.
    Devuyst O.
    Bull Mem Acad R Med Belg; 2004 Oct 14; 159(Pt 2):212-7. PubMed ID: 15615095
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