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Journal Abstract Search

262 related items for PubMed ID: 21932010

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  • 4. [Two cases of Dent disease type 1 with Bartter-like phenotype and literature review].
    Cheng M, Meng X, Liu M, Gong CX.
    Zhonghua Yi Xue Za Zhi; 2024 Sep 03; 104(34):3256-3259. PubMed ID: 39193613
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  • 6. Pediatric Dent disease presenting with rickets and end-stage renal disease: case report and literature review.
    Mao Y, Zhang C, Zhou Z, Zhou W, Yin L.
    J Int Med Res; 2024 Sep 03; 52(9):3000605241280048. PubMed ID: 39327974
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  • 7. [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 03; 48(5):329-33. PubMed ID: 20654030
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  • 10. Proteinuria in Dent disease: a review of the literature.
    van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A.
    Pediatr Nephrol; 2017 Oct 03; 32(10):1851-1859. PubMed ID: 27757584
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  • 13. Clinical manifestation and genetic findings in three boys with low molecular Weight Proteinuria - three case reports for exploring Dent Disease and Fanconi syndrome.
    Duan N, Huang C, Pang L, Jiang S, Yang W, Li H.
    BMC Nephrol; 2021 Jan 11; 22(1):24. PubMed ID: 33430795
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  • 16. 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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  • 17. Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3.
    García-Castaño A, Gómez-Conde S, Gondra L, Herrero M, Aguirre M, de la Hoz AB, Castaño L, Renaltube group, Madariaga L.
    Sci Rep; 2023 Aug 03; 13(1):12587. PubMed ID: 37537162
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  • 19. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
    Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R.
    Nephrol Dial Transplant; 2009 May 03; 24(5):1455-64. PubMed ID: 19096086
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