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Journal Abstract Search

65 related items for PubMed ID: 3490570

  • 21. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov; 72(5):690-5. PubMed ID: 6314235
    [Abstract] [Full Text] [Related]

  • 22. Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Wurster KG, Ranke MB, Heilbronner H, Gupta D.
    Endokrinologie; 1982 Oct; 80(2):142-50. PubMed ID: 6984387
    [Abstract] [Full Text] [Related]

  • 23. Defective 11 beta hydroxylation in patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency.
    Kolanowski J, Crabbe J.
    Ann Endocrinol (Paris); 1981 Dec; 42(6):537-8. PubMed ID: 6980618
    [No Abstract] [Full Text] [Related]

  • 24. [Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case].
    Zacharías S, Contreras P.
    Rev Chil Obstet Ginecol; 1984 Dec; 49(5):295-9. PubMed ID: 6242254
    [No Abstract] [Full Text] [Related]

  • 25. Late-onset 21-hydroxylase deficiency and polycystic ovary disease. A case report.
    Balkin MS, Altchek A.
    J Reprod Med; 1986 Jun; 31(6):517-9. PubMed ID: 3488399
    [Abstract] [Full Text] [Related]

  • 26. [A case of 17 alpha-hydroxylase deficiency with bone anomalies (author's transl)].
    Itatsu T, Naitoh K, Matsuda N, Matsui N.
    Nihon Naika Gakkai Zasshi; 1980 Aug 10; 69(8):960-6. PubMed ID: 6970788
    [No Abstract] [Full Text] [Related]

  • 27. [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]

  • 28. Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair.
    Turan S, Bereket A, Guran T, Akcay T, Papari-Zareei M, Auchus RJ.
    Eur J Endocrinol; 2009 Feb 15; 160(2):325-30. PubMed ID: 18996963
    [Abstract] [Full Text] [Related]

  • 29. 17 alpha-hydroxylation deficiency.
    Biglieri EG, Kater CE.
    Endocrinol Metab Clin North Am; 1991 Jun 15; 20(2):257-68. PubMed ID: 1879398
    [Abstract] [Full Text] [Related]

  • 30. [Incomplete P450 17 alpha enzyme deficiency: report of six cases].
    Tian QJ, Zhang YW, Lu ZL, Sha GH, Gao H.
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct 15; 42(10):670-4. PubMed ID: 18241541
    [Abstract] [Full Text] [Related]

  • 31. Assessment of the role of laparoscopic ovarian biopsy.
    Fayez JA, Jonas HS.
    Obstet Gynecol; 1976 Oct 15; 48(4):397-402. PubMed ID: 135212
    [Abstract] [Full Text] [Related]

  • 32. 17α‑hydroxylase/17,20‑lyase deficiency in congenital adrenal hyperplasia: A case report.
    Xu S, Hu S, Yu X, Zhang M, Yang Y.
    Mol Med Rep; 2017 Jan 15; 15(1):339-344. PubMed ID: 27959413
    [Abstract] [Full Text] [Related]

  • 33. Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis.
    Tvedegaard E, Frederiksen V, Olgaard K, Nielsen MD, Starup J.
    Acta Endocrinol (Copenh); 1981 Oct 15; 98(2):267-73. PubMed ID: 6270940
    [Abstract] [Full Text] [Related]

  • 34. Testicular in vitro conversion of progesterone to testosterone and androstenedione in 17 alpha-hydroxylase deficiency.
    Salti IS, Hajj H, Dhib-Jalbut S.
    J Steroid Biochem; 1982 Aug 15; 17(2):155-7. PubMed ID: 6981031
    [Abstract] [Full Text] [Related]

  • 35. Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17 alpha-hydroxylase cytochrome P-450.
    Yanase T, Kagimoto M, Matsui N, Simpson ER, Waterman MR.
    Mol Cell Endocrinol; 1988 Oct 15; 59(3):249-53. PubMed ID: 3263289
    [Abstract] [Full Text] [Related]

  • 36. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries.
    Mallin SR.
    Ann Intern Med; 1969 Jan 15; 70(1):69-75. PubMed ID: 4303304
    [No Abstract] [Full Text] [Related]

  • 37. Adrenal steroidogenesis in heterozygotes for 21-hydroxylase deficiency.
    Child DF, Bu'lock DE, Anderson DC.
    Clin Endocrinol (Oxf); 1979 Oct 15; 11(4):391-8. PubMed ID: 316370
    [No Abstract] [Full Text] [Related]

  • 38. 17α-hydroxlyase/17, 20-lyase deficiency in three siblings with primary amenorrhea and absence of secondary sexual development.
    Oh YK, Ryoo U, Kim D, Cho SY, Jin DK, Yoon BK, Lee DY, Choi D.
    J Pediatr Adolesc Gynecol; 2012 Oct 15; 25(5):e103-5. PubMed ID: 22841373
    [Abstract] [Full Text] [Related]

  • 39. [17-alpha-hydroxylase deficiency--a case report].
    Kashiwai K, Hiraishi E, Miyashita R, Ienaga N, Murakami A.
    Horumon To Rinsho; 1983 Jun 15; 31 Suppl():124-6. PubMed ID: 6604597
    [No Abstract] [Full Text] [Related]

  • 40. Male pseudohermaphroditism as a cause of secondary hypertension: a case report.
    Aydin Z, Ozturk S, Gursu M, Uzun S, Karadag S, Kazancioglu R.
    Endocrine; 2010 Aug 15; 38(1):100-3. PubMed ID: 20960109
    [Abstract] [Full Text] [Related]

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