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PUBMED FOR HANDHELDS

Journal Abstract Search


80 related items for PubMed ID: 3490570

  • 1. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 4. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar; 12(3):193-6. PubMed ID: 2786019
    [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; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 6. [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; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. 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]

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

  • 10. [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]

  • 11. Identification of new steroids in patients with 17 alpha-hydroxylase deficiency by capillary gas chromatography/mass spectrometry.
    Blau N, Zachmann M, Kempken B, Staudenmann W, Möhr E, Curtius HC.
    Biomed Environ Mass Spectrom; 1987 Nov 10; 14(11):633-7. PubMed ID: 2962669
    [Abstract] [Full Text] [Related]

  • 12. Arrest of follicular development in a patient with 17 alpha-hydroxylase deficiency: folliculogenesis in association with a lack of estrogen synthesis in the ovaries.
    Araki S, Chikazawa K, Sekiguchi I, Yamauchi H, Motoyama M, Tamada T.
    Fertil Steril; 1987 Jan 10; 47(1):169-72. PubMed ID: 3491767
    [Abstract] [Full Text] [Related]

  • 13. Steroid responsive hypertension secondary to 11-beta hydroxylase deficiency--a case report.
    Isiavwe AR, Ekpebegh CO, Fasanmade OA, Ohwovoriole AE.
    West Afr J Med; 2008 Jul 10; 27(3):182-5. PubMed ID: 19256327
    [Abstract] [Full Text] [Related]

  • 14. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 10; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 15. Steroid spectrum in human urine as revealed by gas chromatography V. Identification and quantitation of 3 alpha, 20 alpha-dihydroxy-5-beta pregnan-11-one (11-keto-pregnanediol) during different stages of development in children with C/21 hydroxylase deficiency.
    Kecskés L, Czira G.
    Acta Biochim Biophys Acad Sci Hung; 1981 Apr 10; 16(3-4):179-88. PubMed ID: 6982583
    [Abstract] [Full Text] [Related]

  • 16. A genetic male patient with 17 alpha-hydroxylase deficiency.
    Jones HW, Lee PA, Rock JA, Archer DF, Migeon CJ.
    Obstet Gynecol; 1982 Feb 10; 59(2):254-9. PubMed ID: 6979016
    [Abstract] [Full Text] [Related]

  • 17. In vitro fertilization and primary embryonic cleavage are possible in 17 alpha-hydroxylase deficiency despite extremely low intrafollicular 17 beta-estradiol.
    Rabinovici J, Blankstein J, Goldman B, Rudak E, Dor Y, Pariente C, Geier A, Lunenfeld B, Mashiach S.
    J Clin Endocrinol Metab; 1989 Mar 10; 68(3):693-7. PubMed ID: 2493041
    [Abstract] [Full Text] [Related]

  • 18. Amenorrhea related to progestin excess in congenital adrenal hyperplasia.
    Rosenfield RL, Bickel S, Razdan AK.
    Obstet Gynecol; 1980 Aug 10; 56(2):208-15. PubMed ID: 7393510
    [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 10; 19(6):473-9. PubMed ID: 6121730
    [Abstract] [Full Text] [Related]

  • 20. [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 Dec 10; 23(2):137-40. PubMed ID: 8040569
    [Abstract] [Full Text] [Related]


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