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Journal Abstract Search

135 related items for PubMed ID: 3491009

  • 1. [A case of 21-hydroxylase deficiency and Bartter's syndrome associated with a balanced 6-9 translocation].
    Yabe R, Mizuno K, Ojima M, Ogawa S, Hashimoto S, Kunii N, Kishino K, Tani M, Niimura S, Watari H.
    Nihon Naibunpi Gakkai Zasshi; 1986 Aug 20; 62(8):843-56. PubMed ID: 3491009
    [Abstract] [Full Text] [Related]

  • 2. 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 Aug 20; 18(5-6):333-49. PubMed ID: 3333163
    [Abstract] [Full Text] [Related]

  • 3. [A case with Bartter's syndrome associated with type II hyperlipidemia, increased fluidity of plasma VLDL and abnormal configuration of peripheral erythrocytes (author's transl)].
    Imai T, Makino K, Takeda N, Nakamura S, Endo Y, Okuyama M, Miura K, Iida H, Kawade M.
    Nihon Naibunpi Gakkai Zasshi; 1982 Feb 20; 58(2):131-47. PubMed ID: 7044842
    [Abstract] [Full Text] [Related]

  • 4. [A case of glucocorticoid-responsive hyperaldosteronism: follow-up study for 21 years--comparison with cases of 17 alpha-hydroxylase deficiency in Japan].
    Murase H, Yamakita N, Yasuda K, Noritake N, Mercado-Asis LB, Takeuchi K, Murakami O, Abe K, Yoshinaga K, Miura K.
    Nihon Naibunpi Gakkai Zasshi; 1990 Jan 20; 66(1):50-82. PubMed ID: 2407572
    [Abstract] [Full Text] [Related]

  • 5. [Malignant arterial hypertension disclosing late congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency].
    Ribstein J, Sciolla JP, Barjon P, Sultan C, Forest M, de Peretti E.
    Arch Mal Coeur Vaiss; 1988 Jun 20; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 6. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr 20; 21(2):128-34. PubMed ID: 6750188
    [Abstract] [Full Text] [Related]

  • 7. Long-term follow-up of a girl with the neonatal form of Bartter's syndrome.
    Nakagawa Y, Toya K, Natsume H, Nasuda K, Takeuchi H, Kubota A, Ogawa H, Igarashi Y.
    Endocr J; 1997 Apr 20; 44(2):275-81. PubMed ID: 9228463
    [Abstract] [Full Text] [Related]

  • 8. [Pseudo-Bartter's syndrome induced by surreptitious ingestion of furosemide to lose weight: a case report and possible pathophysiology].
    Sasaki H, Kawasaki T, Yamamoto T, Ninomiya H, Ono J, Yamamoto T, Asano T, Okumura M, Kangawa K, Matsuo H.
    Nihon Naibunpi Gakkai Zasshi; 1986 Aug 20; 62(8):867-81. PubMed ID: 3023152
    [Abstract] [Full Text] [Related]

  • 9. An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension.
    Morimoto I, Maeda R, Izumi M, Ishimaru T, Nishimori I, Nagataki S.
    J Clin Endocrinol Metab; 1983 May 20; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 10. Familial Bartter's syndrome and the effect of indomethacin in one family member.
    Tsunoda S, Tsushima T, Nishioka T, Ohno N, Fukunaga T, Takano K, Yumura W, Shizume K, Branch RA.
    J Urol; 1982 May 20; 127(5):1000-5. PubMed ID: 7086975
    [Abstract] [Full Text] [Related]

  • 11. Association of Bartter's syndrome and empty sella.
    Ertekin V, Selimoglu AM, Orbak Z.
    J Pediatr Endocrinol Metab; 2003 Sep 20; 16(7):1065-8. PubMed ID: 14513887
    [Abstract] [Full Text] [Related]

  • 12. [Endocrinological analysis before and after living-related renal transplantation in a patient of Bartter's syndrome].
    Yokoyama T.
    Nihon Jinzo Gakkai Shi; 1995 Oct 20; 37(10):580-6. PubMed ID: 7474511
    [Abstract] [Full Text] [Related]

  • 13. Dexamethasone-suppressible hyperaldosteronism. Adrenal transition cell hyperplasia?
    Connell JM, Kenyon CJ, Corrie JE, Fraser R, Watt R, Lever AF.
    Hypertension; 1986 Aug 20; 8(8):669-76. PubMed ID: 3015796
    [Abstract] [Full Text] [Related]

  • 14. Role of prostaglandins in the pathogenesis of Bartter's syndrome.
    Fichman MP, Telfer N, Zia P, Speckart P, Golub M, Rude R.
    Am J Med; 1976 May 31; 60(6):785-97. PubMed ID: 798488
    [Abstract] [Full Text] [Related]

  • 15. The effect of amiloride on the renin-aldosterone system in primary hyperaldosteronism and Bartter's syndrome.
    Griffing GT, Aurecchia SA, Sindler BH, Melby JC.
    J Clin Pharmacol; 1982 May 31; 22(11-12):505-12. PubMed ID: 6761369
    [Abstract] [Full Text] [Related]

  • 16. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 17. Adult-onset familial adrenal 21-hydroxylase deficiency.
    Blankstein J, Faiman C, Reyes FI, Schroeder ML, Winter JS.
    Am J Med; 1980 Mar 07; 68(3):441-8. PubMed ID: 6965821
    [Abstract] [Full Text] [Related]

  • 18. The natural history of salt-wasting disorders of adrenal and renal origin.
    Rösler A.
    J Clin Endocrinol Metab; 1984 Oct 07; 59(4):689-700. PubMed ID: 6384251
    [Abstract] [Full Text] [Related]

  • 19. Effects of indomethacin on the vascular abnormalities of Bartter's syndrome.
    Richards CJ, Mark AL, Van Orden DE, Kaloyanides GJ.
    Circulation; 1978 Sep 07; 58(3 Pt 1):544-9. PubMed ID: 679446
    [Abstract] [Full Text] [Related]

  • 20. [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
    [Abstract] [Full Text] [Related]

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