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356 related items for PubMed ID: 32860533

  • 1. Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.
    Gianesello L, Del Prete D, Anglani F, Calò LA.
    Hum Genet; 2021 Mar; 140(3):401-421. PubMed ID: 32860533
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  • 2. Proteinuria in Dent disease: a review of the literature.
    van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A.
    Pediatr Nephrol; 2017 Oct; 32(10):1851-1859. PubMed ID: 27757584
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  • 3. Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
    Deng H, Zhang Y, Xiao H, Yao Y, Zhang H, Liu X, Su B, Guan N, Zhong X, Wang S, Ding J, Wang F.
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1306. PubMed ID: 32495484
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  • 5. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
    Drosataki E, Maragkou S, Dermitzaki K, Stavrakaki I, Lygerou D, Latsoudis H, Pleros C, Petrakis I, Zaganas I, Stylianou K.
    BMC Nephrol; 2022 May 12; 23(1):182. PubMed ID: 35549682
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  • 7. Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria.
    Sekine T, Komoda F, Miura K, Takita J, Shimadzu M, Matsuyama T, Ashida A, Igarashi T.
    Nephrol Dial Transplant; 2014 Feb 12; 29(2):376-84. PubMed ID: 24081861
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  • 9. Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.
    Mansour-Hendili L, Blanchard A, Le Pottier N, Roncelin I, Lourdel S, Treard C, González W, Vergara-Jaque A, Morin G, Colin E, Holder-Espinasse M, Bacchetta J, Baudouin V, Benoit S, Bérard E, Bourdat-Michel G, Bouchireb K, Burtey S, Cailliez M, Cardon G, Cartery C, Champion G, Chauveau D, Cochat P, Dahan K, De la Faille R, Debray FG, Dehoux L, Deschenes G, Desport E, Devuyst O, Dieguez S, Emma F, Fischbach M, Fouque D, Fourcade J, François H, Gilbert-Dussardier B, Hannedouche T, Houillier P, Izzedine H, Janner M, Karras A, Knebelmann B, Lavocat MP, Lemoine S, Leroy V, Loirat C, Macher MA, Martin-Coignard D, Morin D, Niaudet P, Nivet H, Nobili F, Novo R, Faivre L, Rigothier C, Roussey-Kesler G, Salomon R, Schleich A, Sellier-Leclerc AL, Soulami K, Tiple A, Ulinski T, Vanhille P, Van Regemorter N, Jeunemaître X, Vargas-Poussou R.
    Hum Mutat; 2015 Aug 12; 36(8):743-52. PubMed ID: 25907713
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  • 11. [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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  • 12. An atypical Dent's disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes.
    Addis M, Meloni C, Tosetto E, Ceol M, Cristofaro R, Melis MA, Vercelloni P, Del Prete D, Marra G, Anglani F.
    Eur J Hum Genet; 2013 Jun 02; 21(6):687-90. PubMed ID: 23047739
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  • 13. Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
    Ye Q, Shen Q, Rao J, Zhang A, Zheng B, Liu X, Shen Y, Chen Z, Wu Y, Hou L, Jian S, Wei M, Ma M, Sun S, Li Q, Dang X, Wang Y, Xu H, Mao J, for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of National Center for Children's Care.
    Clin Genet; 2020 Mar 02; 97(3):407-417. PubMed ID: 31674016
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  • 17. [Clinical and genetic analysis of Dent disease in 4 Chinese children].
    Jian S, Wei M, He YY, Wang W, Kang YL, Sun ZX.
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Dec 02; 17(12):1261-6. PubMed ID: 26695661
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  • 20. 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 Dec 02; 4():492. PubMed ID: 26389017
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