These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

78 related items for PubMed ID: 2691923

  • 1. [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]

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

  • 3. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
    Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L.
    Pediatr Med Chir; 1987 Jul; 9(3):309-10. PubMed ID: 2823235
    [Abstract] [Full Text] [Related]

  • 4. 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]

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

  • 6. [Male pseudohermaphroditism due to 17-alpha-hydroxylase deficiency].
    Bartolucci L, Fioretti M, Rossi G, Commissari R, Valori C.
    Minerva Endocrinol; 1995 Dec; 20(4):237-41. PubMed ID: 8709921
    [Abstract] [Full Text] [Related]

  • 7. [Late discovery of female pseudo-hermaphroditism by complete blockade 21-hydroxylase (author's transl)].
    Heim J, Massart C, Lémée F, Amice-Chambon V.
    Nouv Presse Med; 1981 Dec 26; 10(47):3841-3. PubMed ID: 6977130
    [Abstract] [Full Text] [Related]

  • 8. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 26; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 9. A female pseudohermaphrodite with salt losing congenital adrenal hyperplasia as the result of 21--beta--OH deficiency.
    Preeyasombat C, Siripoonya P, Tejavej A, Pitchayayothin N.
    J Med Assoc Thai; 1975 Mar 26; 58(3):61-9. PubMed ID: 1127377
    [No Abstract] [Full Text] [Related]

  • 10. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 26; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 11. [Causes of ambiguous external genitalia in neonates].
    Zdravković D, Milenković T, Sedlecki K, Guć-Sćekić M, Rajić V, Banićević M.
    Srp Arh Celok Lek; 2001 Aug 26; 129(3-4):57-60. PubMed ID: 11534268
    [Abstract] [Full Text] [Related]

  • 12. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar 26; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

  • 13. [Medroxyprogesterone acetate. Contributive treatment in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in children].
    La Selve H, Sempé M, Morel Y, Forest MG, de Peretti E, David M.
    Arch Fr Pediatr; 1985 Mar 26; 42(7):511-6. PubMed ID: 2935112
    [Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. 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]

  • 16. 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]

  • 17. [Congenital adrenal hyperplasia as a cause of female pseudo- hermaphroditism].
    Larrea F, Ulloa-Aguirre A, Pérez-Palacios G.
    Rev Invest Clin; 1986 Feb 10; 38(2):209-17. PubMed ID: 3526493
    [No Abstract] [Full Text] [Related]

  • 18. Primary adrenal insufficiency with hypertension. A case report on partial primary adrenal insufficiency and partial 11-beta-hydroxylase deficiency.
    van Deijk WA, Blom PS, VD Vijver JC.
    Neth J Med; 1979 Feb 10; 22(6):191-4. PubMed ID: 316501
    [No Abstract] [Full Text] [Related]

  • 19. [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]

  • 20. [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]

    Page: [Next] [New Search]
    of 4.