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Journal Abstract Search

151 related items for PubMed ID: 8040569

  • 1. [Primary amenorrhea and arterial hypertension in a case of 17 alpha-hydroxylase deficiency].
    Martin-Du Pan RC, Dahoun S, Stalberg A, Campana A.
    J Gynecol Obstet Biol Reprod (Paris); 1994; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]

  • 2. [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; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 3. 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; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 4. [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; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 5. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB, Loucopoulos A, Jewelewicz R.
    J Reprod Med; 1992 Mar; 37(3):242-6. PubMed ID: 1564711
    [Abstract] [Full Text] [Related]

  • 6. A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters.
    Espinosa-Herrera F, Espín E, Tito-Álvarez AM, Beltrán LJ, Gómez-Correa D, Burgos G, Llamos A, Zurita C, Rojas S, Dueñas-Espín I, Cueva-Ludeña K, Salazar-Vega J, Pinto-Basto J.
    Gynecol Endocrinol; 2020 Jan; 36(1):24-29. PubMed ID: 31464148
    [Abstract] [Full Text] [Related]

  • 7. A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation.
    Guenego A, Morel Y, Ionesco O, Mallet D, Priou-Guesdon M.
    Ann Endocrinol (Paris); 2015 Feb; 76(1):71-4. PubMed ID: 25613935
    [Abstract] [Full Text] [Related]

  • 8. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries.
    Mallin SR.
    Ann Intern Med; 1969 Jan; 70(1):69-75. PubMed ID: 4303304
    [No Abstract] [Full Text] [Related]

  • 9. 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; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 10. The unique patterns of plasma aldosterone and 18-hydroxycorticosterone concentrations in the 17 alpha-hydroxylase deficiency syndrome.
    Kater CE, Biglieri EG, Brust N, Chang B, Hirai J.
    J Clin Endocrinol Metab; 1982 Aug; 55(2):295-302. PubMed ID: 7045152
    [No Abstract] [Full Text] [Related]

  • 11. Primary amenorrhoea with hypertension due to 17-hydroxylase deficiency. Therapy with dexamethasone and ethinyloestradiol.
    de Lange WE, Weeke A, Artz W, Jansen W, Doorenbos H.
    Acta Med Scand; 1973 Jun; 193(6):565-71. PubMed ID: 4721967
    [No Abstract] [Full Text] [Related]

  • 12. Primary amenorrhea.
    Radwanska E.
    Obstet Gynecol Annu; 1981 Jun; 10():313-48. PubMed ID: 7024876
    [No Abstract] [Full Text] [Related]

  • 13. Hypergonadotropic amenorrhea and premature ovarian failure: a review.
    Rebar RW.
    J Reprod Med; 1982 Apr; 27(4):179-86. PubMed ID: 6808131
    [Abstract] [Full Text] [Related]

  • 14. 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; 50(2):e68-70. PubMed ID: 19296015
    [Abstract] [Full Text] [Related]

  • 15. Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency.
    Britten FL, Ulett KB, Duncan EL, Perry-Keene DA.
    Med J Aust; 2013 Oct 21; 199(8):556-8. PubMed ID: 24138383
    [No Abstract] [Full Text] [Related]

  • 16. Clinical, hormonal, ovarian, and genetic aspects of 46,XX patients with congenital adrenal hyperplasia due to CYP17A1 defects.
    Carvalho LC, Brito VN, Martin RM, Zamboni AM, Gomes LG, Inácio M, Mermejo LM, Coeli-Lacchini F, Teixeira VR, Gonçalves FT, Carrilho AJ, Del Toro Camargo KY, Finkielstain GP, Taboada GF, Frade Costa EM, Domenice S, Mendonca BB.
    Fertil Steril; 2016 Jun 21; 105(6):1612-9. PubMed ID: 26920256
    [Abstract] [Full Text] [Related]

  • 17. [Strategy for studying mineralocorticoids other than aldosterone in arterial hypertension of hormonal origin].
    Roger M, Nahoul K, Laloy E, Scholler R.
    Ann Med Interne (Paris); 1983 Jun 21; 134(3):238-41. PubMed ID: 6625419
    [Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Trends Endocrinol Metab; 2008 Apr 10; 19(3):96-9. PubMed ID: 18294861
    [Abstract] [Full Text] [Related]

  • 20. [The diagnostic procedure in primary amenorrhea].
    Kumschick H, Hauser GA.
    Schweiz Med Wochenschr; 1966 Aug 20; 96(33):1055-65. PubMed ID: 5997652
    [No Abstract] [Full Text] [Related]

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