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Journal Abstract Search

203 related items for PubMed ID: 11045400

  • 1.
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  • 2. Familial renal tubular acidosis.
    Alper SL.
    J Nephrol; 2010; 23 Suppl 16():S57-76. PubMed ID: 21170890
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  • 3. Renal tubular acidosis--underrated problem?
    Golembiewska E, Ciechanowski K.
    Acta Biochim Pol; 2012; 59(2):213-7. PubMed ID: 22693689
    [Abstract] [Full Text] [Related]

  • 4. Molecular basis of proximal renal tubular acidosis.
    Igarashi T, Sekine T, Watanabe H.
    J Nephrol; 2002; 15 Suppl 5():S135-41. PubMed ID: 12027212
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  • 5. Hereditary distal renal tubular acidosis: new understandings.
    Batlle D, Ghanekar H, Jain S, Mitra A.
    Annu Rev Med; 2001; 52():471-84. PubMed ID: 11160790
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  • 8. Inherited renal tubular acidosis.
    Shayakul C, Alper SL.
    Curr Opin Nephrol Hypertens; 2000 Sep; 9(5):541-6. PubMed ID: 10990375
    [Abstract] [Full Text] [Related]

  • 9. Unraveling the molecular pathogenesis of isolated proximal renal tubular acidosis.
    Igarashi T, Sekine T, Inatomi J, Seki G.
    J Am Soc Nephrol; 2002 Aug; 13(8):2171-7. PubMed ID: 12138151
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  • 12. ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.
    Hahn H, Kang HG, Ha IS, Cheong HI, Choi Y.
    Am J Kidney Dis; 2003 Jan; 41(1):238-43. PubMed ID: 12500243
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  • 14. Renal tubular acidosis.
    Rodríguez-Soriano J, Vallo A.
    Pediatr Nephrol; 1990 May; 4(3):268-75. PubMed ID: 2205272
    [Abstract] [Full Text] [Related]

  • 15. Hyperkalemic Forms of Renal Tubular Acidosis: Clinical and Pathophysiological Aspects.
    Batlle D, Arruda J.
    Adv Chronic Kidney Dis; 2018 Jul; 25(4):321-333. PubMed ID: 30139459
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  • 17. Familial pure proximal renal tubular acidosis--a clinical and genetic study.
    Katzir Z, Dinour D, Reznik-Wolf H, Nissenkorn A, Holtzman E.
    Nephrol Dial Transplant; 2008 Apr; 23(4):1211-5. PubMed ID: 17881426
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  • 19. Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies.
    Haque SK, Ariceta G, Batlle D.
    Nephrol Dial Transplant; 2012 Dec; 27(12):4273-87. PubMed ID: 23235953
    [Abstract] [Full Text] [Related]

  • 20. Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation.
    Piret SE, Gorvin CM, Trinh A, Taylor J, Lise S, Taylor JC, Ebeling PR, Thakker RV.
    Am J Med Genet A; 2016 Nov; 170(11):2988-2992. PubMed ID: 27540713
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