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Journal Abstract Search

277 related items for PubMed ID: 25088262

  • 61. Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD).
    Sweeney WE, Avner ED.
    Cell Tissue Res; 2006 Dec; 326(3):671-85. PubMed ID: 16767405
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  • 63. Kidney enlargement and multiple liver cyst formation implicate mutations in PKD1/2 in adult sporadic polycystic kidney disease.
    Fujimaru T, Mori T, Sekine A, Mandai S, Chiga M, Kikuchi H, Ando F, Mori Y, Nomura N, Iimori S, Naito S, Okado T, Rai T, Hoshino J, Ubara Y, Uchida S, Sohara E.
    Clin Genet; 2018 Jul; 94(1):125-131. PubMed ID: 29520754
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  • 66. [Clinical and pathological study of 47 cases with Alport syndrome].
    He X, Liu GL, Xia ZK, Ren XG, Gao YF, Fan ZM, Fu YF, Fu J, Gao CL, Mao S, Chen R.
    Zhonghua Er Ke Za Zhi; 2008 Dec; 46(12):914-8. PubMed ID: 19134254
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  • 68. 2008 Homer W. Smith Award: insights into the pathogenesis of polycystic kidney disease from gene discovery.
    Harris PC.
    J Am Soc Nephrol; 2009 Jun; 20(6):1188-98. PubMed ID: 19423684
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  • 69. Salt-Losing Tubulopathies in Children: What's New, What's Controversial?
    Kleta R, Bockenhauer D.
    J Am Soc Nephrol; 2018 Mar; 29(3):727-739. PubMed ID: 29237739
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  • 72. [Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease].
    Magistroni R, Izzi C, Scolari F.
    G Ital Nefrol; 2016 Mar; 33(2):. PubMed ID: 27067212
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  • 73. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J.
    Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
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  • 74. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.
    Shaer AJ.
    Am J Med Sci; 2001 Dec; 322(6):316-32. PubMed ID: 11780689
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  • 76. Abdominal sonographic study of autosomal dominant polycystic kidney disease.
    Nicolau C, Torra R, Bianchi L, Vilana R, Gilabert R, Darnell A, Brú C.
    J Clin Ultrasound; 2000 Dec; 28(6):277-82. PubMed ID: 10867665
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  • 80. [Clinical practice guidelines for polycystic kidney diseases].
    Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Xu D, Mei C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar 10; 37(3):277-283. PubMed ID: 32128744
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