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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

47 related articles for article (PubMed ID: 691437)

  • 1. [17 alpha-hydroxylase deficiency].
    Yoshinaga K
    Nihon Rinsho; 1978 May; Suppl():1580-1. PubMed ID: 691437
    [No Abstract]   [Full Text] [Related]  

  • 2. [Corticoadrenal congenital hyperplasia with loss of salts due to 21-hydroxylase deficiency. Presentation of a personal observation].
    Gandullia E; de Langlade E; Marchese N
    Minerva Pediatr; 1976 Jun; 28(22):1437-42. PubMed ID: 948345
    [No Abstract]   [Full Text] [Related]  

  • 3. Partial adrenocortical hydroxylase deficiency syndrome in infertile women.
    Loran Z; Roitman A; Pollack MS; Dupont B
    Fertil Steril; 1980 Jul; 34(1):76. PubMed ID: 6249647
    [No Abstract]   [Full Text] [Related]  

  • 4. Detection of heterozygote of 21-hydroxylase deficiency.
    Levine LS; Pang S; Dupont B; Pollack M; Lorenzen F; New MI
    Lancet; 1980 Mar; 1(8168 Pt 1):603-4. PubMed ID: 6102330
    [No Abstract]   [Full Text] [Related]  

  • 5. [Case of 21-OHlase deficient adrenal gland hyperplasia developing the initial symptoms of adrenal hypofunction with a salt-losing tendency at the 5th month of age].
    Nozaki Y; Kato Y; Shimizu S; Oyama K; Amamiya S
    Horumon To Rinsho; 1978 Nov; 26(11):1189-96. PubMed ID: 719924
    [No Abstract]   [Full Text] [Related]  

  • 6. 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; 58(3):61-9. PubMed ID: 1127377
    [No Abstract]   [Full Text] [Related]  

  • 7. Posterior fusion without clitoromegaly in a female with partial 21-hydroxylase deficiency.
    Wolff PB; Wilbois RP; Weldon VV; Haymond MW
    J Pediatr; 1977 Dec; 91(6):951-2. PubMed ID: 597374
    [No Abstract]   [Full Text] [Related]  

  • 8. Female phenotype in a male child due to 17-alpha-hydroxylase deficiency.
    Heremans GF; Moolenaar AJ; van Gelderen HH
    Arch Dis Child; 1976 Sep; 51(9):721-3. PubMed ID: 999330
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Main enzymatic disorders of the adrenal cortex and their therapeutic possibilities].
    Teofili MT; Vecchi L
    Clin Ter; 1978 Jul; 86(2):161-78. PubMed ID: 743857
    [No Abstract]   [Full Text] [Related]  

  • 11. Dynamics of adrenal steroidogenesis in childhood: changes in the excretion of 16-oxygenated- and 11-oxygenated-steroids by 21-hydroxylase deficient children at various ages.
    Kecskés L
    Endokrinologie; 1982 Oct; 80(2):151-7. PubMed ID: 6297879
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H; Shimizu N
    Nihon Rinsho; 1979 Jun; 37(6):1253-9. PubMed ID: 384051
    [No Abstract]   [Full Text] [Related]  

  • 13. [17 alpha-hydroxylase deficiency].
    Kumagi R
    Nihon Rinsho; 1977; 35 Suppl 1():1096-7. PubMed ID: 306453
    [No Abstract]   [Full Text] [Related]  

  • 14. Plasma deoxycorticosterone radioimmunoassay: method and clinical applications.
    Mantero F; Sonino N; Masarotto P
    J Nucl Biol Med; 1975; 19(4):186-94. PubMed ID: 1223252
    [No Abstract]   [Full Text] [Related]  

  • 15. Masculinizing operation for a female patient with congenital adrenocortical hyperplasia due to 21-hydroxylase deficiency.
    Okuyama A; Takiuchi H; Kajikawa H; Tada Y; Namiki M; Nakano E; Takaha M
    Hinyokika Kiyo; 1985 Nov; 31(11):2003-5. PubMed ID: 3879104
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Proceedings: Case of probable 17 alpha-hydroxylase deficiency].
    Miura K; Kojima M; Mihara A; Endo Y; Kato K
    Nihon Naibunpi Gakkai Zasshi; 1974 Feb; 50(2):533. PubMed ID: 4476556
    [No Abstract]   [Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 21(4):247-56. PubMed ID: 559816
    [No Abstract]   [Full Text] [Related]  

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

  • 20. [Plasmatic 17-alpha-hydroxyprogesterone in congenital adrenal hyperplasia due to 21 hydroxylase deficiency, treated and untreated].
    Loras B; Roux H; Audi-Parera L; David M; Bertrand J
    Biomedicine; 1974 Jul; 21(7):317-22. PubMed ID: 4373095
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.