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266 related items for PubMed ID: 8897553

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [The Gitelman syndrome--a differential diagnosis of Bartter syndrome].
    Zimmermann J, Reincke M, Schramm L, Harlos J, Allolio B.
    Med Klin (Munich); 1994 Dec 15; 89(12):640-4. PubMed ID: 7869998
    [Abstract] [Full Text] [Related]

  • 3. Bartter's and Gitelman's syndromes: from gene to clinic.
    Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D.
    Nephron Physiol; 2004 Dec 15; 96(3):p65-78. PubMed ID: 15056980
    [Abstract] [Full Text] [Related]

  • 4. Miscellaneous non-inflammatory musculoskeletal conditions. Bartter's and Gitelman's diseases.
    Favero M, Calò LA, Schiavon F, Punzi L.
    Best Pract Res Clin Rheumatol; 2011 Oct 15; 25(5):637-48. PubMed ID: 22142744
    [Abstract] [Full Text] [Related]

  • 5. Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
    Barakat AJ, Rennert OM.
    J Nephrol; 2001 Oct 15; 14(1):43-7. PubMed ID: 11281344
    [Abstract] [Full Text] [Related]

  • 6. Molecular pathophysiology of Bartter's and Gitelman's syndromes.
    Koulouridis E, Koulouridis I.
    World J Pediatr; 2015 May 15; 11(2):113-25. PubMed ID: 25754753
    [Abstract] [Full Text] [Related]

  • 7. Paradoxes in magnesium transport in type 1 Bartter's syndrome and Gitelman's syndrome: a modeling analysis.
    Dutta P, Layton AT.
    Am J Physiol Renal Physiol; 2024 Sep 01; 327(3):F386-F396. PubMed ID: 38991009
    [Abstract] [Full Text] [Related]

  • 8. The molecular genetic approach to "Bartter's syndrome".
    Károlyi L, Koch MC, Grzeschik KH, Seyberth HW.
    J Mol Med (Berl); 1998 Apr 01; 76(5):317-25. PubMed ID: 9587066
    [Abstract] [Full Text] [Related]

  • 9. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.
    Simon DB, Lifton RP.
    Am J Physiol; 1996 Nov 01; 271(5 Pt 2):F961-6. PubMed ID: 8945989
    [Abstract] [Full Text] [Related]

  • 10. [Hypokalemic metabolic alkalosis: apropos of a case of Gitelman's syndrome].
    Puchades MJ, González Rico MA, Pons S, Miguel A, Bonilla B.
    Nefrologia; 2004 Nov 01; 24 Suppl 3():72-5. PubMed ID: 15219074
    [Abstract] [Full Text] [Related]

  • 11. Gitelman's syndrome: an overlooked cause of chronic hypokalemia and hypomagnesemia in adults.
    Schepkens H, Lameire N.
    Acta Clin Belg; 2001 Nov 01; 56(4):248-54. PubMed ID: 11603254
    [Abstract] [Full Text] [Related]

  • 12. Gitelman's syndrome (Bartter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred.
    Pollak MR, Delaney VB, Graham RM, Hebert SC.
    J Am Soc Nephrol; 1996 Oct 01; 7(10):2244-8. PubMed ID: 8915985
    [Abstract] [Full Text] [Related]

  • 13. 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 Oct 01; 55(4-5):219-23. PubMed ID: 12398028
    [Abstract] [Full Text] [Related]

  • 14. Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome.
    Yahata K, Tanaka I, Kotani M, Mukoyama M, Ogawa Y, Goto M, Nakagawa M, Sugawara A, Tanaka K, Shimatsu A, Nakao K.
    Am J Kidney Dis; 1999 Nov 01; 34(5):845-53. PubMed ID: 10561140
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 65(10):571-4. PubMed ID: 9809361
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 12(1):24-30. PubMed ID: 8528245
    [Abstract] [Full Text] [Related]

  • 17. Hypokalemic metabolic alkalosis with hypomagnesuric hypermagnesemia and severe hypocalciuria: a new syndrome?
    Mehrotra R, Nolph KD, Kathuria P, Dotson L.
    Am J Kidney Dis; 1997 Jan 01; 29(1):106-14. PubMed ID: 9002538
    [Abstract] [Full Text] [Related]

  • 18. Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: report of two cases.
    Tsukamoto T, Kobayashi T, Kawamoto K, Fukase M, Chihara K.
    Am J Kidney Dis; 1995 Apr 01; 25(4):637-41. PubMed ID: 7702064
    [Abstract] [Full Text] [Related]

  • 19. Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.
    Simon DB, Lifton RP.
    Adv Nephrol Necker Hosp; 1997 Apr 01; 27():343-59. PubMed ID: 9408455
    [No Abstract] [Full Text] [Related]

  • 20. Mimicry of surreptitious diuretic ingestion and the ability to make a genetic diagnosis.
    Schepkens H, Hoeben H, Vanholder R, Lameire N.
    Clin Nephrol; 2001 Mar 01; 55(3):233-7. PubMed ID: 11316244
    [Abstract] [Full Text] [Related]

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