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PUBMED FOR HANDHELDS

Journal Abstract Search


194 related items for PubMed ID: 20807608

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  • 43. Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience.
    Kasap Demir B, Mutlubaş F, Soyaltın E, Alparslan C, Arya M, Alaygut D, Arslansoyu Çamlar S, Berdeli A, Yavaşcan Ö.
    Turk J Med Sci; 2021 Apr 30; 51(2):772-777. PubMed ID: 33315352
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  • 44. DNA testing for live kidney donors at risk for autosomal dominant polycystic kidney disease.
    Huang E, Samaniego-Picota M, McCune T, Melancon JK, Montgomery RA, Ugarte R, Kraus E, Womer K, Rabb H, Watnick T.
    Transplantation; 2009 Jan 15; 87(1):133-7. PubMed ID: 19136903
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  • 45. [Genetics and genetic counseling].
    Izzi C, Liut F, Dallera N, Mazza C, Magistroni R, Savoldi G, Scolari F.
    G Ital Nefrol; 2016 Jan 15; 33(2):. PubMed ID: 27067213
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  • 46. Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.
    Zhao X, Paterson AD, Zahirieh A, He N, Wang K, Pei Y.
    Clin J Am Soc Nephrol; 2008 Jan 15; 3(1):146-52. PubMed ID: 18077784
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  • 51. Recurrent fetal loss associated with bilineal inheritance of type 1 autosomal dominant polycystic kidney disease.
    Paterson AD, Wang KR, Lupea D, St George-Hyslop P, Pei Y.
    Am J Kidney Dis; 2002 Jul 15; 40(1):16-20. PubMed ID: 12087556
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  • 52. DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease.
    Coto E, Sanz de Castro S, Aguado S, Alvarez J, Arias M, Menéndez MJ, López-Larrea C.
    J Med Genet; 1995 Jun 15; 32(6):442-5. PubMed ID: 7666395
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  • 55. [Mutational analysis of the PKD1 and PKD2 (type 1 and 2 dominant autosomal polycystic kidney) genes].
    Torra R, Badenas C, Pérez-Oller L, San Millán JL, Tellería D, Estivill X, Darnell A.
    Nefrologia; 2000 Jun 15; 20(1):39-46. PubMed ID: 10822721
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  • 56. Incident renal events and risk factors in autosomal dominant polycystic kidney disease: a population and family-based cohort followed for 22 years.
    Dicks E, Ravani P, Langman D, Davidson WS, Pei Y, Parfrey PS.
    Clin J Am Soc Nephrol; 2006 Jul 15; 1(4):710-7. PubMed ID: 17699277
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  • 60. Novel method for genomic analysis of PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease.
    Tan YC, Blumenfeld JD, Anghel R, Donahue S, Belenkaya R, Balina M, Parker T, Levine D, Leonard DG, Rennert H.
    Hum Mutat; 2009 Feb 15; 30(2):264-73. PubMed ID: 18837007
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