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Journal Abstract Search

89 related items for PubMed ID: 5596279

  • 1. [Familial proteinuria of the tubular type with appearance of the Bartter syndrome in 1 of the members of the family: a new disease?].
    François R, Bertrand J, Pellet, Salle B, Moreau P, Manuel P.
    J Urol Nephrol (Paris); 1967; 73(10):829-39. PubMed ID: 5596279
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  • 2. [Bartter's disease associated with hypercorticism, phosphate and magnesium deficiencies and familial renal tubular disease].
    Sann L, Moreau P, Longin B, Sassard J, François R.
    Arch Fr Pediatr; 1975 Apr; 32(4):350-66. PubMed ID: 1164148
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  • 4. Chronic hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism ("Bartter's syndrome"), and hypercalciuria. Report of two cases with emphasis on natural history and on catch-up growth during treatment.
    Fanconi A, Schachenmann G, Nüssli R, Prader A.
    Helv Paediatr Acta; 1971 Jun; 26(2):144-63. PubMed ID: 5139245
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  • 6. Urologic considerations in Bartter's syndrome.
    Dehart HS, Bath NM, Glenn JF, Gunnells JC.
    J Urol; 1974 Apr; 111(4):420-4. PubMed ID: 4819361
    [No Abstract] [Full Text] [Related]

  • 7. Primary aldosteronism. A study of carbohydrate tolerance and the juxtaglomerular apparatus.
    Haddock L, Tristani FE, Morales JO, Aguiló F.
    Bol Asoc Med P R; 1967 Oct; 59(10):435-44. PubMed ID: 5258113
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  • 8. [Renal diabetes insipidus with hypokalemia, hyperaldosteronism, and increased plasma-renin activity (Bartter syndrome)].
    Rosenkranz A, Smolka T.
    Padiatr Padol; 1973 Oct; 8(3):297-303. PubMed ID: 4715039
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  • 10. Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
    Lloyd SE, Pearce SH, Günther W, Kawaguchi H, Igarashi T, Jentsch TJ, Thakker RV.
    J Clin Invest; 1997 Mar 01; 99(5):967-74. PubMed ID: 9062355
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  • 11. Hypokalemic metabolic alkalosis--three case reports.
    Galesić K, Bozić B, Sćukanec-Spoljar M, Morović-Vergles J, Cvitković-Kuzmić A, Ljubanović D.
    Acta Med Croatica; 2001 Mar 01; 55(4-5):219-23. PubMed ID: 12398028
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  • 12. [Renal tubular hypomagnesemia of familial origin].
    Rapado A, Pedraza M, Torrijos A, Moreno F, Aparicio A, Sánchez-Alarcón J.
    Rev Clin Esp; 1985 Apr 01; 176(6):302-4. PubMed ID: 4001489
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  • 14. [Electrophoretic analysis of proteinurias encountered in the course of renal tubular disorders].
    Traeger J, François R, Creyssel R, Revillard JP, Manuel Y, Freycon MT, Site M.
    J Urol Nephrol (Paris); 1965 Sep 01; 71(9):728-35. PubMed ID: 5859057
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  • 18. [The paradoxic behavior of the kidney in Bartter's syndrome and other processes].
    Méndez Aparicio FM.
    Rev Clin Esp; 1980 Oct 31; 159(2):107-14. PubMed ID: 7209032
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