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Journal Abstract Search

392 related items for PubMed ID: 11281344

  • 21. Clinical, biochemical and molecular genetic data in five children with Gitelman's syndrome.
    Schmidt H, Kabesch M, Schwarz HP, Kiess W.
    Horm Metab Res; 2001 Jun; 33(6):354-7. PubMed ID: 11456284
    [Abstract] [Full Text] [Related]

  • 22. Identification of novel mutations in Na-Cl cotransporter gene in a Korean patient with atypical Gitelman's syndrome.
    Yoo TH, Lee SH, Yoon K, Baek H, Chung JH, Lee T, Ihm C, Kim M.
    Am J Kidney Dis; 2003 Dec; 42(6):E11-6. PubMed ID: 14655226
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

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

  • 25. [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; 36(4):583-7. PubMed ID: 16078592
    [Abstract] [Full Text] [Related]

  • 26. Genetic renal disorders with hypomagnesemia and hypocalciuria.
    Knoers NV, de Jong JC, Meij IC, Van Den Heuvel LP, Bindels RJ.
    J Nephrol; 2003 Jul; 16(2):293-6. PubMed ID: 12768080
    [Abstract] [Full Text] [Related]

  • 27. [Gitelman's syndrome--a differential diagnosis in hypokalemia].
    Hovland A, Bjørbaek E, Leren TP.
    Tidsskr Nor Laegeforen; 2004 Apr 22; 124(8):1093-4. PubMed ID: 15114386
    [Abstract] [Full Text] [Related]

  • 28. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.
    Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA, Lifton RP.
    Nat Genet; 1996 Jun 22; 13(2):183-8. PubMed ID: 8640224
    [Abstract] [Full Text] [Related]

  • 29. Four novel mutations in the thiazide-sensitive Na-Cl co-transporter gene in Japanese patients with Gitelman's syndrome.
    Maki N, Komatsuda A, Wakui H, Ohtani H, Kigawa A, Aiba N, Hamai K, Motegi M, Yamaguchi A, Imai H, Sawada K.
    Nephrol Dial Transplant; 2004 Jul 22; 19(7):1761-6. PubMed ID: 15069170
    [Abstract] [Full Text] [Related]

  • 30. Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia.
    Nakamura A, Shimizu C, Nagai S, Yoshida M, Aoki K, Kondo T, Miyoshi H, Wada N, Tajima T, Terauchi Y, Yoshioka N, Koike T.
    Clin Endocrinol (Oxf); 2010 Feb 22; 72(2):272-6. PubMed ID: 19508680
    [Abstract] [Full Text] [Related]

  • 31. 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 22; 2(6):340-6; quiz 347. PubMed ID: 16932456
    [Abstract] [Full Text] [Related]

  • 32. Attenuated renal excretion in response to thiazide diuretics in Gitelman's syndrome: a case report.
    Yeum CH, Kim SW, Ma SK, Ko JH, Nah MY, Kim NH, Choi KC.
    J Korean Med Sci; 2002 Aug 22; 17(4):567-70. PubMed ID: 12172059
    [Abstract] [Full Text] [Related]

  • 33. Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter.
    Lin SH, Cheng NL, Hsu YJ, Halperin ML.
    Am J Kidney Dis; 2004 Feb 22; 43(2):304-12. PubMed ID: 14750096
    [Abstract] [Full Text] [Related]

  • 34. [Gitelman syndrome in children: true hypokalemia but false Bartter syndrome].
    Fischbach M, Hoellinger MJ, Tersic J, Matz B, Mengus L, Desprez P, Chaigne D, Stoll C, Taimi A, Simeoni U.
    Arch Pediatr; 1994 Oct 22; 1(10):916-8. PubMed ID: 7842074
    [Abstract] [Full Text] [Related]

  • 35. Chondrocalcinosis secondary to hypomagnesemia in Gitelman's syndrome.
    Ea HK, Blanchard A, Dougados M, Roux C.
    J Rheumatol; 2005 Sep 22; 32(9):1840-2. PubMed ID: 16142886
    [Abstract] [Full Text] [Related]

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  • 37. Hypokalemia and the pathology of ion transport molecules.
    Antes LM, Kujubu DA, Fernandez PC.
    Semin Nephrol; 1998 Jan 22; 18(1):31-45. PubMed ID: 9459287
    [Abstract] [Full Text] [Related]

  • 38. [Tubolopaties associated to hypokalemia].
    Capasso G.
    G Ital Nefrol; 2004 Jan 22; 21(1):73-83. PubMed ID: 15356851
    [Abstract] [Full Text] [Related]

  • 39. Abnormal renal magnesium handling.
    Sutton RA, Domrongkitchaiporn S.
    Miner Electrolyte Metab; 1993 Jan 22; 19(4-5):232-40. PubMed ID: 8264509
    [Abstract] [Full Text] [Related]

  • 40. A case of Gitelman's syndrome with decreased angiotensin II-forming activity.
    Eto K, Onaka U, Tsuchihashi T, Hirano T, Nakayama M, Masutani K, Hirakata H, Urata H, Yasujima M.
    Hypertens Res; 2006 Jul 22; 29(7):545-9. PubMed ID: 17044667
    [Abstract] [Full Text] [Related]

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