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Journal Abstract Search

97 related items for PubMed ID: 6976525

  • 1. Hypokalemic myopathy associated with 17 alpha-hydroxylase deficiency: a case report.
    Yazaki K, Kuribayashi T, Yamamura Y, Kurihara T, Araki S.
    Neurology; 1982 Jan; 32(1):94-7. PubMed ID: 6976525
    [Abstract] [Full Text] [Related]

  • 2. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H, Shimizu N.
    Nihon Rinsho; 1979 Jun 10; 37(6):1253-9. PubMed ID: 384051
    [No Abstract] [Full Text] [Related]

  • 3. Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency.
    Scott JS.
    Br J Obstet Gynaecol; 1981 Jun 10; 88(6):688. PubMed ID: 6972781
    [No Abstract] [Full Text] [Related]

  • 4. 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 10; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 5. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb 10; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 6. Hypokalemic rhabdomyolysis in a child with 11-hydroxylase deficiency.
    Atabek ME, Pirgon O, Sert A.
    J Pediatr Endocrinol Metab; 2008 Jan 10; 21(1):93-6. PubMed ID: 18404978
    [Abstract] [Full Text] [Related]

  • 7. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity.
    Fraser R, Brown JJ, Mason PA, Morton JJ, Lever AF, Robertson JI, Lee HA, Miller H.
    J Hum Hypertens; 1987 Jun 10; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 8. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 10; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 9. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar 10; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

  • 10. A case of 17 alpha-hydroxylase deficiency syndrome associated with right adrenal tumor.
    Ogawa K, Hara A, Tanabe S, Tamori S, Yoshida H, Pak CH, Matsunaga M, Kawai C, Dodo H, Tanimura H.
    Clin Exp Hypertens A; 1984 Mar 10; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 11. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature].
    De Marinis L, Mancini A, Saporosi A, Calabrò F, Massari M, Moneta E, Menini E, Barbarino A.
    Minerva Ginecol; 1989 Jul 10; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 12. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr 10; 21(2):128-34. PubMed ID: 6750188
    [Abstract] [Full Text] [Related]

  • 13. Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency. A case report.
    Abad L, Parrilla JJ, Marcos J, Gimeno F, López Bernal A.
    Br J Obstet Gynaecol; 1980 Dec 10; 87(12):1162-5. PubMed ID: 6254560
    [Abstract] [Full Text] [Related]

  • 14. Molecular basis of hypokalemic myopathy caused by 17alpha-hydroxylase/17,20-lyase deficiency.
    Satoh J, Kuroda Y, Nawata H, Yanase T.
    Neurology; 1998 Dec 10; 51(6):1748-51. PubMed ID: 9855540
    [Abstract] [Full Text] [Related]

  • 15. [Deficiency of 17 alpha-hydroxylase. Presentation of 3 new cases].
    Gómez Sáez JM, Romero González R, Soler Ramón J, Bonnin Lafuenta R, Porta Martí M.
    Med Clin (Barc); 1984 Mar 10; 82(9):407-9. PubMed ID: 6609291
    [No Abstract] [Full Text] [Related]

  • 16. A case of hypokalemic myopathy associated with transient hypothyroidism.
    Kanemaru Y, Aizawa K, Kagami T, Haraguchi K, Onaya T.
    Endocrinol Jpn; 1984 Dec 10; 31(6):809-14. PubMed ID: 6532797
    [Abstract] [Full Text] [Related]

  • 17. [A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency with high levels of plasma aldosterone and angiotensin II].
    Toyoda N, Murata K, Tanaka Y, Kawai Y, Yamamoto T, Nishiyama Y, Matsumoto T, Sugiyama Y.
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Jul 10; 38(7):1162-5. PubMed ID: 3091739
    [No Abstract] [Full Text] [Related]

  • 18. [A case of 17 alpha-hydroxylase deficiency with male pseudohermaphroditism (author's transl)].
    Taura K, Tashiro T, Fujimatsu S, Noboru S, Ishizaki T, Hakariya H, Tokunaga T, Matsuo S, Iida K, Hara K, Yokota M, Kawai K.
    Nihon Naibunpi Gakkai Zasshi; 1980 Jun 20; 56(6):843-54. PubMed ID: 6967832
    [Abstract] [Full Text] [Related]

  • 19. 17 alpha-hydroxylase deficiency in a genetic male and female sibling pair.
    Sills IN, MacGillivray MH, Amrhein JA, Migeon CJ, Peterson RE.
    Int J Gynaecol Obstet; 1981 Dec 20; 19(6):473-9. PubMed ID: 6121730
    [Abstract] [Full Text] [Related]

  • 20. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency and hormonal profiles in the nuclear family.
    Rohmer V, Barbot N, Bertrand P, Nahoul K, Bigorgne JC, Forest MG.
    J Clin Endocrinol Metab; 1990 Aug 20; 71(2):523-9. PubMed ID: 2166072
    [Abstract] [Full Text] [Related]

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