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Journal Abstract Search

93 related items for PubMed ID: 2691923

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [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]

  • 23.
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  • 24. [Bilateral testicular hypertrophy and congenital adrenal hyperplasia caused by 11-beta-hydroxylase deficiency].
    Khaldi F, Bennaceur B, Hamza M, Boudina T, Jafoura H, Hamza B.
    Arch Fr Pediatr; 1987 Jul 15; 44(7):513-6. PubMed ID: 3501279
    [Abstract] [Full Text] [Related]

  • 25. [Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Boutte P, Madar H, d'Ollone M, Ferracci JP, Bebin B, Lambert JC, Sebag F.
    Pediatrie; 1986 Jul 15; 41(7):559-64. PubMed ID: 3493478
    [Abstract] [Full Text] [Related]

  • 26. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr 15; 21(2):128-34. PubMed ID: 6750188
    [Abstract] [Full Text] [Related]

  • 27. Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency. A case report.
    Abad L, Parrilla JJ, Marcos J, Gimeno F, López Bernal A.
    Br J Obstet Gynaecol; 1980 Dec 15; 87(12):1162-5. PubMed ID: 6254560
    [Abstract] [Full Text] [Related]

  • 28.
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  • 29. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 15; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 30. [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 15; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. The 17 alpha-hydroxylase deficiency found in genotypically female and male siblings, both phenotypically female.
    Ito S, Yamaguchi M, Miyamoto N, Yanase T.
    Jinrui Idengaku Zasshi; 1977 Mar 15; 21(4):247-56. PubMed ID: 559816
    [No Abstract] [Full Text] [Related]

  • 33. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb 15; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 34. 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 15; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 35. Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
    Roger M, Merceron RE, Girard F, Canlorbe P, Dehennin L, Konopka P, Seneze J, Toublanc JE.
    Horm Res; 1982 Jun 15; 16(1):23-31. PubMed ID: 6279481
    [Abstract] [Full Text] [Related]

  • 36. Genetic aspects of congenital adrenal hyperplasia.
    Dacou-Voutetakis C, Maniati-Christidi M, Dracopoulou-Vabouli M.
    J Pediatr Endocrinol Metab; 2001 Jun 15; 14 Suppl 5():1303-8; discussion 1317. PubMed ID: 11964027
    [Abstract] [Full Text] [Related]

  • 37. [Current concepts in the treatment of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    David M, Bertrand J, Kemlin I, François R.
    Pediatrie; 1981 Mar 15; 36(2):161-6. PubMed ID: 6972030
    [No Abstract] [Full Text] [Related]

  • 38. 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]

  • 39. 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 Jun 15; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 40. Hypokalemic myopathy associated with 17 alpha-hydroxylase deficiency: a case report.
    Yazaki K, Kuribayashi T, Yamamura Y, Kurihara T, Araki S.
    Neurology; 1982 Jan 15; 32(1):94-7. PubMed ID: 6976525
    [Abstract] [Full Text] [Related]

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