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Journal Abstract Search

59 related items for PubMed ID: 6604597

  • 1. [17-alpha-hydroxylase deficiency--a case report].
    Kashiwai K, Hiraishi E, Miyashita R, Ienaga N, Murakami A.
    Horumon To Rinsho; 1983 Jun; 31 Suppl():124-6. PubMed ID: 6604597
    [No Abstract] [Full Text] [Related]

  • 2. [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 Jun; 49(5):295-9. PubMed ID: 6242254
    [No Abstract] [Full Text] [Related]

  • 3. [Report on 3 cases of 17 alpha-hydroxylase deficiency].
    Zhang ZJ.
    Zhonghua Nei Ke Za Zhi; 1983 Sep; 22(9):565-7. PubMed ID: 6606541
    [No Abstract] [Full Text] [Related]

  • 4. [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 Sep; 41(7):559-64. PubMed ID: 3493478
    [Abstract] [Full Text] [Related]

  • 5. [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; 36(2):161-6. PubMed ID: 6972030
    [No Abstract] [Full Text] [Related]

  • 6. [17 alpha-hydroxylase deficiency].
    Kumagi R.
    Nihon Rinsho; 1977 Mar; 35 Suppl 1():1096-7. PubMed ID: 306453
    [No Abstract] [Full Text] [Related]

  • 7. [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]

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

  • 9. [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; 38(7):1162-5. PubMed ID: 3091739
    [No Abstract] [Full Text] [Related]

  • 10. [Case of salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency and a short stature caused by early closure of epiphyseal lines in spite of steroid replacement therapy].
    Kondo T, Ueda K, Saito H, Horiuchi Y.
    Horumon To Rinsho; 1983 Jul; 31(7):637-43. PubMed ID: 6605823
    [No Abstract] [Full Text] [Related]

  • 11. [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]

  • 12. [Research on hirsutism. Apropos of a case of partial 21-hydroxylase deficiency].
    Gheron G.
    Nouv Presse Med; 1981 Oct 24; 10(38):3163. PubMed ID: 6974855
    [No Abstract] [Full Text] [Related]

  • 13. [17 alpha-hydroxylase deficiency syndrome with hyperaldosteronism. A case report].
    Monno S, Furukawa K, Matsuzawa K, Furuta S.
    Nihon Naika Gakkai Zasshi; 1987 Oct 24; 76(10):1565-72. PubMed ID: 3325588
    [No Abstract] [Full Text] [Related]

  • 14. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
    Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L.
    Pediatr Med Chir; 1987 Oct 24; 9(3):309-10. PubMed ID: 2823235
    [Abstract] [Full Text] [Related]

  • 15. [Congenital adrenal hyperplasia as a result of 21-hydroxylase block. Review of 10 cases].
    Belhadj H, Ezzaouia G, Chammakhi S, Bouguerra R, Boukhris R.
    Tunis Med; 1986 Mar 24; 64(3):243-8. PubMed ID: 3490029
    [No Abstract] [Full Text] [Related]

  • 16. [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 Mar 24; 44(7):513-6. PubMed ID: 3501279
    [Abstract] [Full Text] [Related]

  • 17. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar 24; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 18. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr 24; 92():79-82. PubMed ID: 2164496
    [Abstract] [Full Text] [Related]

  • 19. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L.
    Minerva Pediatr; 1976 Jun 23; 28(22):1443-4. PubMed ID: 986003
    [No Abstract] [Full Text] [Related]

  • 20. Late-onset 21-hydroxylase deficiency and polycystic ovary disease. A case report.
    Balkin MS, Altchek A.
    J Reprod Med; 1986 Jun 23; 31(6):517-9. PubMed ID: 3488399
    [Abstract] [Full Text] [Related]

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