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

153 related items for PubMed ID: 3486896

  • 1. Spontaneous sexual development and menarche in a female with 17 alpha-hydroxylase deficiency.
    Singhellakis PN, Panidis D, Papadimas J, Demertzi H, Tsourdis A, Sotsiou F, Ikkos DG.
    J Endocrinol Invest; 1986 Apr; 9(2):177-83. PubMed ID: 3486896
    [Abstract] [Full Text] [Related]

  • 2. A case of 17 alpha-hydroxylase deficiency syndrome associated with right adrenal tumor.
    Ogawa K, Hara A, Tanabe S, Tamori S, Yoshida H, Pak CH, Matsunaga M, Kawai C, Dodo H, Tanimura H.
    Clin Exp Hypertens A; 1984 Apr; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 3. Congenital 17 alpha-hydroxylase deficiency: a clinicopathologic study.
    Sasano H, Masuda T, Ojima M, Fukuchi S, Sasano N.
    Hum Pathol; 1987 Oct; 18(10):1002-7. PubMed ID: 3653875
    [Abstract] [Full Text] [Related]

  • 4. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.
    Couillin P, Rappaport R, Kuttenn F, Canlorbe P, Hors J, Marcelli-Barge A, Feingold J, Grisard MC, Boué J, Boué A.
    Tissue Antigens; 1982 Feb; 19(2):100-7. PubMed ID: 6980498
    [No Abstract] [Full Text] [Related]

  • 5. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.
    New MI, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine LS.
    J Clin Endocrinol Metab; 1979 Feb; 48(2):356-9. PubMed ID: 218988
    [Abstract] [Full Text] [Related]

  • 6. The 21-hydroxylase activity in the glomerulosa and fasciculata of the adrenal cortex in congenital adrenal hyperplasia.
    Kuhnle U, Chow D, Rapaport R, Pang S, Levine LS, New MI.
    J Clin Endocrinol Metab; 1981 Mar; 52(3):534-44. PubMed ID: 6257750
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr; 92():79-82. PubMed ID: 2164496
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Renin-angiotensin-aldosterone system: a long-term follow-up study in 17 alpha-hydroxylase deficiency syndrome (17OHDS).
    Scaroni C, Opocher G, Mantero F.
    Clin Exp Hypertens A; 1986 Apr; 8(4-5):773-80. PubMed ID: 3530552
    [Abstract] [Full Text] [Related]

  • 12. Zona glomerulosa function after life-long suppression in two siblings with the hypertensive virilizing form of congenital adrenal hyperplasia.
    Rodríguez Portales JA, Arteaga E, López Moreno JM, Biglieri EG.
    J Clin Endocrinol Metab; 1988 Feb; 66(2):349-54. PubMed ID: 3276723
    [Abstract] [Full Text] [Related]

  • 13. 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; 22(6):191-4. PubMed ID: 316501
    [No Abstract] [Full Text] [Related]

  • 14. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Winkel CA, Casey ML, Worley RJ, Madden JD, MacDonald PC.
    J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
    [Abstract] [Full Text] [Related]

  • 15. 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]

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

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
    de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G.
    Hypertension; 1985 Sep; 7(2):204-10. PubMed ID: 2984117
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Hypertension in a neonate with 11 beta-hydroxylase deficiency.
    Mimouni M, Kaufman H, Roitman A, Morag C, Sadan N.
    Eur J Pediatr; 1985 Jan; 143(3):231-3. PubMed ID: 3872797
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.