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Journal Abstract Search

172 related items for PubMed ID: 38726999

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  • 4. 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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  • 5. 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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  • 7. Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts.
    Beara-Lasic L, Cogal A, Mara K, Enders F, Mehta RA, Haskic Z, Furth SL, Trachtman H, Scheinman SJ, Milliner DS, Goldfarb DS, Harris PC, Lieske JC, investigators of the Rare Kidney Stone Consortium.
    Pediatr Nephrol; 2020 Apr 12; 35(4):633-640. PubMed ID: 30852663
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  • 8. 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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  • 9. Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations.
    Li F, Yue Z, Xu T, Chen M, Zhong L, Liu T, Jing X, Deng J, Hu B, Liu Y, Wang H, Lai KN, Sun L, Liu J, Maxwell PH, Wang Y.
    J Pediatr; 2016 Jul 31; 174():204-210.e1. PubMed ID: 27174143
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  • 10. Observations of a large Dent disease cohort.
    Blanchard A, Curis E, Guyon-Roger T, Kahila D, Treard C, Baudouin V, Bérard E, Champion G, Cochat P, Dubourg J, de la Faille R, Devuyst O, Deschenes G, Fischbach M, Harambat J, Houillier P, Karras A, Knebelmann B, Lavocat MP, Loirat C, Merieau E, Niaudet P, Nobili F, Novo R, Salomon R, Ulinski T, Jeunemaître X, Vargas-Poussou R.
    Kidney Int; 2016 Aug 31; 90(2):430-439. PubMed ID: 27342959
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  • 11. 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 31; 10(3):275-7. PubMed ID: 25124980
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  • 13. Dent disease in Poland: what we have learned so far?
    Zaniew M, Mizerska-Wasiak M, Załuska-Leśniewska I, Adamczyk P, Kiliś-Pstrusińska K, Haliński A, Zawadzki J, Lipska-Ziętkiewicz BS, Pawlaczyk K, Sikora P, Ludwig M, Szczepańska M.
    Int Urol Nephrol; 2017 Nov 31; 49(11):2005-2017. PubMed ID: 28815356
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  • 15. Renal manifestations of Dent disease and Lowe syndrome.
    Cho HY, Lee BH, Choi HJ, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2008 Feb 31; 23(2):243-9. PubMed ID: 18038239
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  • 19. [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 31; 48(5):329-33. PubMed ID: 20654030
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  • 20. 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 31; 36(12):1151-1158. PubMed ID: 29058463
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