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Journal Abstract Search

443 related items for PubMed ID: 6498022

  • 1. [Development of tetany in siblings suffered from Bartter's syndrome].
    Suitsu N, Kita S, Okamoto S, Kimura S, Shiozaki Y.
    No To Shinkei; 1984 Aug; 36(8):749-54. PubMed ID: 6498022
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  • 3. Bartter's syndrome: an autosomal recessive disorder? Study of four patients in one generation of the same pedigree and their relatives.
    Hogewind BL, van Brummelen P, Veltkamp JJ.
    Acta Med Scand; 1981 Aug; 209(6):463-7. PubMed ID: 7257865
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  • 4. Familial Bartter's syndrome.
    Ogihara T, Maruyama A, Nugent CA, Hata T, Mikami H, Kumahara Y.
    Arch Intern Med; 1982 May; 142(5):906-8. PubMed ID: 7082115
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  • 5. [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
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  • 6. Bartter's syndrome. Differentiation into two clinical groups.
    Robson WL, Arbus GS, Balfe JW.
    Am J Dis Child; 1979 Jun 15; 133(6):636-8. PubMed ID: 35973
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  • 7. The effect of long-term treatment with spironolactone on sodium pump abnormalities in the red blood cells of patients with Bartter's syndrome.
    Horký K, Schreiber V, Dvoráková J.
    Exp Clin Endocrinol; 1984 Jul 15; 84(1):105-11. PubMed ID: 6090182
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  • 8. [Bartter's syndrome: seven cases in siblings. Hypothesis of mild forms (author's transl)].
    Nivet H, Rolland JC, Lebranchu Y, Dray F, Benatre A, Drucker J, Grenier B, Bagros P.
    Nouv Presse Med; 1980 Apr 19; 9(18):1287-90. PubMed ID: 6990383
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  • 9. A hitherto unreported case of 21-hydroxylase deficiency associated with Bartter's syndrome and a balanced 6-9 translocation.
    Yabe R, Mizuno K, Ojima M, Ogawa S, Tani M, Niimura S, Watari H, Kunii N, Suenaga K, Yatabe Y.
    J Med; 1987 Apr 19; 18(5-6):333-49. PubMed ID: 3333163
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  • 11. Bartter's syndrome in pregnancy: a case report and review.
    O'Sullivan E, Monga M, Graves W.
    Am J Perinatol; 1997 Jan 19; 14(1):55-7. PubMed ID: 9259898
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  • 12. Familial Bartter's syndrome: report of a case with early manifestations and persistent hypercalciuria.
    Girardin E, Favre L, Vallotton MB, Paunier L.
    Helv Paediatr Acta; 1986 Aug 19; 41(3):221-8. PubMed ID: 3759484
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  • 14. Fetal polyuria and hydramnios associated with Bartter's syndrome.
    Sieck UV, Ohlsson A.
    Obstet Gynecol; 1984 Mar 19; 63(3 Suppl):22S-24S. PubMed ID: 6366663
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  • 15. [A case of pseudohypoparathyroidism (PHP) type II associated with Bartter's syndrome--restoration of phosphaturic response to parathyroid hormone (PTH) by treatment for hypopotassemia].
    Bando Y, Miyakoshi H, Nagaoka T, Ohsawa K, Kobayashi K.
    Nihon Naibunpi Gakkai Zasshi; 1992 Jul 20; 68(7):676-87. PubMed ID: 1516722
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  • 17. Association between activating mutations of calcium-sensing receptor and Bartter's syndrome.
    Watanabe S, Fukumoto S, Chang H, Takeuchi Y, Hasegawa Y, Okazaki R, Chikatsu N, Fujita T.
    Lancet; 2002 Aug 31; 360(9334):692-4. PubMed ID: 12241879
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  • 20. [Bartter's syndrome: new classification, old therapy].
    Peco-Antic A, Dudic S, Marsenic O, Zivic G.
    Srp Arh Celok Lek; 2001 Aug 31; 129(5-6):139-42. PubMed ID: 11797462
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