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PUBMED FOR HANDHELDS

Journal Abstract Search


67 related items for PubMed ID: 891369

  • 1. [Primary amenorrhoea, hypertension, and hypokalaemia in 17-hydroxylase deficiency, a not uncommon condition (author's transl)].
    de Lange WE, Lappöhn RE, Sluiter WJ, Doorenbos H.
    Dtsch Med Wochenschr; 1977 Jul 15; 102(28):1024-8. PubMed ID: 891369
    [Abstract] [Full Text] [Related]

  • 2. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 15; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. 17 alpha-hydroxylase deficiency syndrome associated with bilateral streak gonads and impaired development of Müllerian ducts derivatives. Report of a case.
    de Gennes JL, Jambart S, Turpin G, Elkik F, Roger M.
    Acta Endocrinol (Copenh); 1982 May 10; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. 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]

  • 7. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 10; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 8. [Gonadoblastoma in an HY-negative pure XY-gonadal dysgenesis (author's transl)].
    Freundl G, Gebauer HJ, Dolff M.
    Geburtshilfe Frauenheilkd; 1980 Dec 10; 40(12):1093-8. PubMed ID: 6778764
    [Abstract] [Full Text] [Related]

  • 9. [Primary amenorrhoea in a phenotypically female individual with a karyotype 46, xy and bilateral gonadoblastoma (author's transl)].
    Veselý K, Motlík K, Stárka L, Málková J.
    Cesk Gynekol; 1976 Sep 10; 41(7):513-6. PubMed ID: 975314
    [No Abstract] [Full Text] [Related]

  • 10. Congenital adrenal hyperplasia 11beta-hydroxylase deficiency: two cases managed with bilateral adrenalectomy.
    John M, Menon SK, Shah NS, Menon PS.
    Singapore Med J; 2009 Feb 10; 50(2):e68-70. PubMed ID: 19296015
    [Abstract] [Full Text] [Related]

  • 11. The 17 alpha-hydroxylase deficiency found in genotypically female and male siblings, both phenotypically female.
    Ito S, Yamaguchi M, Miyamoto N, Yanase T.
    Jinrui Idengaku Zasshi; 1977 Mar 10; 21(4):247-56. PubMed ID: 559816
    [No Abstract] [Full Text] [Related]

  • 12. [Amenorrhoea and hyperprolactinaemia (author's transl)].
    Tscherne G.
    Wien Klin Wochenschr; 1979 Dec 07; 91(23):790-3. PubMed ID: 538933
    [Abstract] [Full Text] [Related]

  • 13. [The so-called pure gonadal dysgenesis (author's transl)].
    László J, Bösze P, Gaál M.
    Geburtshilfe Frauenheilkd; 1975 Oct 07; 35(10):786-92. PubMed ID: 1183797
    [Abstract] [Full Text] [Related]

  • 14. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Oct 07; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 15. [A case of 17 alpha-hydroxylase deficiency with long stature and epileptic cramps (author's transl)].
    Ono Y.
    Horumon To Rinsho; 1982 Apr 07; 30(4):353-7. PubMed ID: 6980065
    [No Abstract] [Full Text] [Related]

  • 16. 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 07; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 17. [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 07; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 18. [Mineralocorticoid function investigation in 17-hydroxylase deficiency].
    Lefebvre J, Racadot A, Cappoen JP, Fourlinnie JC, Dessaint JP, Linquette M.
    Lille Med; 1971 Nov 07; 16(9):1281-8. PubMed ID: 5138701
    [No Abstract] [Full Text] [Related]

  • 19.
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    [No Abstract] [Full Text] [Related]

  • 20. [Congenital virilizing adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Study of eleven cases (author's transl)].
    Dunand A, Roger M, Chaussain JL, Nocton F, Job JC.
    Sem Hop; 1971 Nov 07; 57(33-36):1392-7. PubMed ID: 6270798
    [Abstract] [Full Text] [Related]


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