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Journal Abstract Search

618 related items for PubMed ID: 20081299

  • 1. Hypomagnesemia: an evidence-based approach to clinical cases.
    Assadi F.
    Iran J Kidney Dis; 2010 Jan; 4(1):13-9. PubMed ID: 20081299
    [Abstract] [Full Text] [Related]

  • 2. Hypomagnesemia: renal magnesium handling.
    Kelepouris E, Agus ZS.
    Semin Nephrol; 1998 Jan; 18(1):58-73. PubMed ID: 9459289
    [Abstract] [Full Text] [Related]

  • 3. Abnormal renal magnesium handling.
    Sutton RA, Domrongkitchaiporn S.
    Miner Electrolyte Metab; 1993 Jan; 19(4-5):232-40. PubMed ID: 8264509
    [Abstract] [Full Text] [Related]

  • 4. [Gitelman syndrome. An overlooked disease with chronic hypomagnesemia and hypokalemia in adults].
    Hansen KW, Mosekilde L.
    Ugeskr Laeger; 2003 Mar 10; 165(11):1123-7. PubMed ID: 12677988
    [Abstract] [Full Text] [Related]

  • 5. [A case of Gitelman's syndrome presenting with severe hypocalcaemia and hypokalemic periodic paralysis].
    Ran XW, Wang C, Dai F, Jiang JJ, Tong NW, Li XJ, Liang JZ.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2005 Jul 10; 36(4):583-7. PubMed ID: 16078592
    [Abstract] [Full Text] [Related]

  • 6. Diagnosis and clinical approach in Gitelman's syndrome.
    Umami V, Oktavia D, Kunmartini S, Wibisana D, Siregar P.
    Acta Med Indones; 2011 Jan 10; 43(1):53-8. PubMed ID: 21339546
    [Abstract] [Full Text] [Related]

  • 7. [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]

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

  • 9. Tacrolimus-associated hypomagnesemia in renal transplant recipients.
    Navaneethan SD, Sankarasubbaiyan S, Gross MD, Jeevanantham V, Monk RD.
    Transplant Proc; 2006 Jun 15; 38(5):1320-2. PubMed ID: 16797291
    [Abstract] [Full Text] [Related]

  • 10. Hypophosphatemia: an evidence-based problem-solving approach to clinical cases.
    Assadi F.
    Iran J Kidney Dis; 2010 Jul 15; 4(3):195-201. PubMed ID: 20622306
    [Abstract] [Full Text] [Related]

  • 11. Ionised and total serum magnesium in renal transplant patients.
    Mazzaferro S, Barberi S, Scarda A, Pasquali M, Rubino F, D'Erasmo E.
    J Nephrol; 2002 Jul 15; 15(3):275-80. PubMed ID: 12113599
    [Abstract] [Full Text] [Related]

  • 12. Gitelman syndrome-associated severe hypokalemia and hypomagnesemia: case report and review of the literature.
    Daskalakis G, Marinopoulos S, Mousiolis A, Mesogitis S, Papantoniou N, Antsaklis A.
    J Matern Fetal Neonatal Med; 2010 Nov 15; 23(11):1301-4. PubMed ID: 20350237
    [Abstract] [Full Text] [Related]

  • 13. Nephrocalcinosis in siblings--familial hypomagnesemia, hypercalciuria with nephrocalcinosis (FHHNC syndrome).
    Prabahar MR, Manorajan R, Fernando ME, Venkatraman R, Balaraman V, Jayakumar M.
    J Assoc Physicians India; 2006 Jun 15; 54():497-500. PubMed ID: 16909703
    [Abstract] [Full Text] [Related]

  • 14. [Hypokalemic metabolic alkalosis: apropos of a case of Gitelman's syndrome].
    Puchades MJ, González Rico MA, Pons S, Miguel A, Bonilla B.
    Nefrologia; 2004 Jun 15; 24 Suppl 3():72-5. PubMed ID: 15219074
    [Abstract] [Full Text] [Related]

  • 15. Gitelman syndrome: report of three cases and literature review.
    Lee YT, Wang IF, Lin TH, Huang CT.
    Kaohsiung J Med Sci; 2006 Jul 15; 22(7):357-62. PubMed ID: 16849105
    [Abstract] [Full Text] [Related]

  • 16. [The treatment of hypomagnesemia].
    van der Sijs IH, Ho-Dac-Pannekeet MM.
    Ned Tijdschr Geneeskd; 2002 May 18; 146(20):934-8. PubMed ID: 12051060
    [Abstract] [Full Text] [Related]

  • 17. Magnesium metabolism in childhood.
    Geven WB, Monnens LA, Willems JL.
    Miner Electrolyte Metab; 1993 May 18; 19(4-5):308-13. PubMed ID: 8264518
    [Abstract] [Full Text] [Related]

  • 18. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): compound heterozygous mutation in the claudin 16 (CLDN16) gene.
    Hampson G, Konrad MA, Scoble J.
    BMC Nephrol; 2008 Sep 24; 9():12. PubMed ID: 18816383
    [Abstract] [Full Text] [Related]

  • 19. Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome.
    Sutton RA, Mavichak V, Halabe A, Wilkins GE.
    Miner Electrolyte Metab; 1992 Sep 24; 18(1):43-51. PubMed ID: 1406504
    [Abstract] [Full Text] [Related]

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