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Journal Abstract Search

243 related items for PubMed ID: 35549682

  • 21. [Clinical characteristics and molecular genetics of Dent's disease: an update].
    Zhang J, Xia ZK.
    Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):909-12. PubMed ID: 23324147
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  • 22. 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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  • 23. 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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  • 25. Clinical and laboratory features of Macedonian children with OCRL mutations.
    Tasic V, Lozanovski VJ, Korneti P, Ristoska-Bojkovska N, Sabolic-Avramovska V, Gucev Z, Ludwig M.
    Pediatr Nephrol; 2011 Apr; 26(4):557-62. PubMed ID: 21249396
    [Abstract] [Full Text] [Related]

  • 26. [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; 17(12):1261-6. PubMed ID: 26695661
    [Abstract] [Full Text] [Related]

  • 27. 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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  • 29. The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report.
    Ranawaka R, Sirisena ND, Dayasiri KC, Cogal AG, Lieske JC, Gamage MP, Dissanayake VHW.
    BMC Res Notes; 2017 Oct 30; 10(1):539. PubMed ID: 29084614
    [Abstract] [Full Text] [Related]

  • 30. 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 30; 52(9):3000605241280048. PubMed ID: 39327974
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  • 32. Antenatal Bartter syndrome presenting as hyperparathyroidism with hypercalcemia and hypercalciuria: a case report and review.
    Gross I, Siedner-Weintraub Y, Simckes A, Gillis D.
    J Pediatr Endocrinol Metab; 2015 Jul 30; 28(7-8):943-6. PubMed ID: 25741940
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  • 37. 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 30; 8(4):235-239. PubMed ID: 31687264
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