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Journal Abstract Search

404 related items for PubMed ID: 11797462

  • 21. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.
    Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP.
    Nat Genet; 1996 Jan; 12(1):24-30. PubMed ID: 8528245
    [Abstract] [Full Text] [Related]

  • 22. Chondrocalcinosis is a feature of Gitelman's variant of Bartter's syndrome. A new look at the hypomagnesemia associated with calcium pyrophosphate dihydrate crystal deposition disease.
    Punzi L, Calò L, Schiavon F, Pianon M, Rosada M, Todesco S.
    Rev Rhum Engl Ed; 1998 Oct; 65(10):571-4. PubMed ID: 9809361
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  • 23. Inherited renal tubular defects with hypokalemia.
    Muthukrishnan J, Modi KD, Kumar PJ, Jha R.
    Saudi J Kidney Dis Transpl; 2009 Mar; 20(2):274-7. PubMed ID: 19237818
    [Abstract] [Full Text] [Related]

  • 24. Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome.
    Károlyi L, Ziegler A, Pollak M, Fischbach M, Grzeschik KH, Koch MC, Seyberth HW.
    Pediatr Nephrol; 1996 Oct; 10(5):551-4. PubMed ID: 8897553
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  • 25. Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
    Barakat AJ, Rennert OM.
    J Nephrol; 2001 Oct; 14(1):43-7. PubMed ID: 11281344
    [Abstract] [Full Text] [Related]

  • 26. The molecular genetic approach to "Bartter's syndrome".
    Károlyi L, Koch MC, Grzeschik KH, Seyberth HW.
    J Mol Med (Berl); 1998 Apr; 76(5):317-25. PubMed ID: 9587066
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  • 27. Analyses of subjects with hypokalemic metabolic alkolosis, Gitelman's and Bartter's syndrome.
    Onem Y, Kucukardali Y, Sahan B, Atasoyu EM, Ipcioğlu O, Terekeci H, Solmazgul E, Top C, Oktenli C.
    Ren Fail; 2008 Apr; 30(7):691-4. PubMed ID: 18704817
    [Abstract] [Full Text] [Related]

  • 28. Renal tubular function in children and adolescents with Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome.
    Peters N, Bettinelli A, Spicher I, Basilico E, Metta MG, Bianchetti MG.
    Nephrol Dial Transplant; 1995 Apr; 10(8):1313-9. PubMed ID: 8538920
    [Abstract] [Full Text] [Related]

  • 29. Heterogeneous derangement of cellular sodium metabolism in Bartter's syndrome. Description of two cases and review of the literature.
    Sechi LA, Melis A, Faedda R, Tedde R, Bartoli E.
    Panminerva Med; 1992 Apr; 34(2):85-92. PubMed ID: 1408334
    [Abstract] [Full Text] [Related]

  • 30. [Renal sodium transport abnormality: Gitelman's syndrome and renal sodium transporter].
    Takeuchi K, Taniyama Y, Ito S, Yasujima M.
    Rinsho Byori; 1999 Dec; 47(12):1128-33. PubMed ID: 10639822
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  • 33. [The neonatal form of Bartter's syndrome: current findings in etiology and physiopathology].
    Proesmans WC.
    Verh K Acad Geneeskd Belg; 1992 Dec; 54(3):253-93. PubMed ID: 1413986
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  • 37. A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia.
    Phillips DR, Ahmad KI, Waller SJ, Meisner P, Karet FE.
    Nat Clin Pract Nephrol; 2006 Jun; 2(6):340-6; quiz 347. PubMed ID: 16932456
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  • 38. [Neonatal Bartter disease diagnosed with the detection of a mutation of the KCNJ1 gene which codifies the synthesis of the renal ROMK1 potassium channel].
    García Nieto V, Müller D, van der Vliet W, Claverie-Martín F.
    Nefrologia; 2001 Jun; 21(5):448-55. PubMed ID: 11795013
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