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Journal Abstract Search

137 related items for PubMed ID: 11394095

  • 1. [Hereditary renal tubule diseases].
    Morin D.
    Arch Pediatr; 2001 May; 8 Suppl 2():301s-303s. PubMed ID: 11394095
    [No Abstract] [Full Text] [Related]

  • 2. Molecular pathophysiology of inborn renal Na+ transport defects.
    Greger R.
    Kidney Blood Press Res; 1998 May; 21(2-4):222-5. PubMed ID: 9762839
    [No Abstract] [Full Text] [Related]

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  • 6. Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutants.
    Bell CL, Tenenhouse HS, Scriver CR.
    Ann N Y Acad Sci; 1985 May; 456():398-400. PubMed ID: 3004298
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  • 8. Bartter's, Gitelman's, and Gordon's syndromes. From physiology to molecular biology and back, yet still some unanswered questions.
    Kamel KS, Oh MS, Halperin ML.
    Nephron; 2002 May; 92 Suppl 1():18-27. PubMed ID: 12401934
    [Abstract] [Full Text] [Related]

  • 9. [Molecular genetic changes identified in tubular disorders affecting water-electrolyte transport].
    Urbizu JM, Gainza FJ, Lampreabe I.
    Nefrologia; 2001 May; 21(2):127-36. PubMed ID: 11464646
    [No Abstract] [Full Text] [Related]

  • 10. [Renal tubular hypomagnesemia of familial origin].
    Rapado A, Pedraza M, Torrijos A, Moreno F, Aparicio A, Sánchez-Alarcón J.
    Rev Clin Esp; 1985 Apr; 176(6):302-4. PubMed ID: 4001489
    [No Abstract] [Full Text] [Related]

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  • 12. Molecular basis of inherited disorders of renal solute transport.
    López-Nieto CE, Brenner BM.
    Curr Opin Nephrol Hypertens; 1997 Sep; 6(5):411-21. PubMed ID: 9327198
    [No Abstract] [Full Text] [Related]

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  • 14. Hereditary disorders of potassium homeostasis.
    Warnock DG.
    Best Pract Res Clin Endocrinol Metab; 2003 Dec; 17(4):505-27. PubMed ID: 14687586
    [Abstract] [Full Text] [Related]

  • 15. Molecular genetics and clinical phenotype in heritable disorders of tubular Na+ transport.
    Hildebrandt F.
    Kidney Blood Press Res; 1998 Dec; 21(2-4):217-21. PubMed ID: 9762838
    [No Abstract] [Full Text] [Related]

  • 16. [Erythrocyte sodium transport in children with pseudohypoaldosteronism].
    Uchiyama M, Gomi T, Satokata I, Sakai K.
    Rinsho Byori; 1988 Jun; 36(6):685-8. PubMed ID: 3210317
    [No Abstract] [Full Text] [Related]

  • 17. Renal tubular disorders.
    Walsh SB, Unwin RJ.
    Clin Med (Lond); 2012 Oct; 12(5):476-9. PubMed ID: 23101152
    [No Abstract] [Full Text] [Related]

  • 18. Use of human genetic variation to study membrane transport of amino acids in kidney.
    Scriver CR.
    Am J Dis Child; 1969 Jan; 117(1):4-12. PubMed ID: 4882965
    [No Abstract] [Full Text] [Related]

  • 19. Inborn hypouricemia due to isolated renal tubular defect.
    de Vries A, Sperling O.
    Biomedicine; 1979 Jun; 30(2):75-80. PubMed ID: 476267
    [Abstract] [Full Text] [Related]

  • 20. Familial hypouricemia due to isolated renal tubular abnormality.
    Benjamin D, Sperling O, Weinberg A, Pinkhas J.
    Biomedicine; 1978 Apr; 29(2):54-6. PubMed ID: 667288
    [Abstract] [Full Text] [Related]

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