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Journal Abstract Search

194 related items for PubMed ID: 20807608

  • 1. Diagnosis of autosomal-dominant polycystic kidney disease: an integrated approach.
    Barua M, Pei Y.
    Semin Nephrol; 2010 Jul; 30(4):356-65. PubMed ID: 20807608
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  • 8. PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis.
    Cornec-Le Gall E, Audrézet MP, Renaudineau E, Hourmant M, Charasse C, Michez E, Frouget T, Vigneau C, Dantal J, Siohan P, Longuet H, Gatault P, Ecotière L, Bridoux F, Mandart L, Hanrotel-Saliou C, Stanescu C, Depraetre P, Gie S, Massad M, Kersalé A, Séret G, Augusto JF, Saliou P, Maestri S, Chen JM, Harris PC, Férec C, Le Meur Y.
    Am J Kidney Dis; 2017 Oct; 70(4):476-485. PubMed ID: 28356211
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  • 16. Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney disease.
    Chang MY, Chen HM, Jenq CC, Lee SY, Chen YM, Tian YC, Chen YC, Hung CC, Fang JT, Yang CW, Wu-Chou YH.
    J Hum Genet; 2013 Nov; 58(11):720-7. PubMed ID: 23985799
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  • 17. [Genetic analysis (PKD2) of autosomal dominant polycystic kidney disease].
    Gómez PF, Moro EC, García-Cosmes P, Sarmiento RG, Romo JM.
    Nefrologia; 2009 Nov; 29(6):562-8. PubMed ID: 19936001
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  • 19. Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.
    Reiterová J, Štekrová J, Merta M, Kotlas J, Elišáková V, Lněnička P, Korabečná M, Kohoutová M, Tesař V.
    BMC Nephrol; 2013 Mar 15; 14():59. PubMed ID: 23496908
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  • 20. Aberrant PKD2 splicing due to a presumed novel missense mutation in autosomal-dominant polycystic kidney disease.
    Tan YC, Blumenfeld J, Michaeel A, Donahue S, Balina M, Parker T, Levine D, Rennert H.
    Clin Genet; 2011 Sep 15; 80(3):287-92. PubMed ID: 20950398
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