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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 11642204

  • 1. [Proximal renal tubular dysfunction in insulin-dependent diabetes mellitus].
    García Nieto V, Luis Yanes MI, Callejón A.
    Nefrologia; 2001; 21 Suppl 3():32-8. PubMed ID: 11642204
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  • 4. Adult Fanconi syndrome secondary to kappa-light chain myeloma: improvement of tubular functions after treatment for myeloma.
    Uchida S, Matsuda O, Yokota T, Takemura T, Ando R, Kanemitsu H, Hamaguchi H, Miyake S, Marumo F.
    Nephron; 1990; 55(3):332-5. PubMed ID: 2115147
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  • 6. The adult Fanconi syndrome: observations on etiology, morphology, renal function and mineral metabolism in three patients.
    Lee DB, Drinkard JP, Rosen VJ, Gonick HC.
    Medicine (Baltimore); 1972 Mar; 51(2):107-38. PubMed ID: 5013635
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  • 8. [On various aspects of physiopathology of the renal tubule in childhood].
    Bottone E, Macchia PA, Baldini G, Bani E.
    Minerva Pediatr; 1973 Jul; 25(26):1119-54. PubMed ID: 4356507
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  • 12. Hypouricemia due to renal urate wasting: different types of tubular transport defects.
    Gaspar GA, Puig JG, Mateos FA, Oria CR, Gomez ME, Gil AA.
    Adv Exp Med Biol; 1986 Jul; 195 Pt A():357-63. PubMed ID: 3728167
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  • 13. [Bone and mineral metabolism in renal tubular dysfunction].
    Tanaka H.
    Nihon Jinzo Gakkai Shi; 2007 Jul; 49(4):422-6. PubMed ID: 17578187
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  • 14. Renal tubular transport of urate in Fanconi syndrome.
    Diamond HS, Meisel AD.
    Adv Exp Med Biol; 1977 Jul; 76B():259-65. PubMed ID: 855750
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  • 15. [A case of renal-ocular syndrome with Fanconi syndrome].
    Takeda M, Hirata M, Koni I, Miyazaki R, Tohuku Y, Takeda R.
    Nihon Jinzo Gakkai Shi; 1988 Jan; 30(1):103-9. PubMed ID: 3386007
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  • 18. [Clinical studies of the pathogenesis of renal elimination of hydrogen ions].
    Gatti R, Tassara A.
    Minerva Pediatr; 1967 Apr 21; 19(16):811-5. PubMed ID: 5615201
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  • 19. Biology and genetics of inherited renal tubular disorders.
    van't Hoff WG.
    Exp Nephrol; 1996 Apr 21; 4(5):253-62. PubMed ID: 8931979
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