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 *

72 related articles for article (PubMed ID: 8257919)

  • 1. Adrenal response to adrenocorticotropin hormone and HLA typing of subjects with different degrees of 21-hydroxylase deficiency.
    Elias LL; Voltarelli JC; Moreira AC
    Braz J Med Biol Res; 1993 Feb; 26(2):177-89. PubMed ID: 8257919
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
    Speiser PW; New MI
    J Clin Endocrinol Metab; 1987 Jan; 64(1):86-91. PubMed ID: 3023431
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia.
    Fiet J; Gueux B; Gourmelen M; Kuttenn F; Vexiau P; Couillin P; Pham-Huu-Trung MT; Villette JM; Raux-Demay MC; Galons H
    J Clin Endocrinol Metab; 1988 Apr; 66(4):659-67. PubMed ID: 2831244
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pituitary-adrenal responses to corticotropin-releasing hormone in different degrees of adrenal 21-hydroxylase deficiency.
    Moreira AC; Elias LL
    J Clin Endocrinol Metab; 1992 Jan; 74(1):198-203. PubMed ID: 1309366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA; Rosenwaks Z; Urban MD; Migeon CJ; Bias WD
    J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effects of continued adrenocorticotropin stimulation on the mineralocorticoid hormones in classical and nonclassical simple virilizing types of 21-hydroxylase deficiency.
    Kater CE; Biglieri EG; Wajchenberg B
    J Clin Endocrinol Metab; 1985 Jun; 60(6):1057-62. PubMed ID: 2987285
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Isolated precocious pubarche: an approach.
    Balducci R; Boscherini B; Mangiantini A; Morellini M; Toscano V
    J Clin Endocrinol Metab; 1994 Aug; 79(2):582-9. PubMed ID: 8045980
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Lorenzen F; Pang S; New MI; Dupont B; Pollack M; Chow DM; Levine LS
    Pediatr Res; 1979 Dec; 13(12):1356-60. PubMed ID: 230448
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Absence of nonclassical congenital adrenal hyperplasia in patients with precocious adrenarche.
    Morris AH; Reiter EO; Geffner ME; Lippe BM; Itami RM; Mayes DM
    J Clin Endocrinol Metab; 1989 Oct; 69(4):709-15. PubMed ID: 2550505
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cortisol response to adrenocorticotropin testing in non-classical congenital adrenal hyperplasia (NCCAH).
    Karachaliou FH; Kafetzi M; Dracopoulou M; Vlachopapadopoulou E; Leka S; Fotinou A; Michalacos S
    J Pediatr Endocrinol Metab; 2016 Dec; 29(12):1365-1371. PubMed ID: 27849625
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
    Charmandari E; Matthews DR; Johnston A; Brook CG; Hindmarsh PC
    J Clin Endocrinol Metab; 2001 Oct; 86(10):4679-85. PubMed ID: 11600525
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency.
    Feuillan P; Pang S; Schürmeyer T; Avgerinos PC; Chrousos GP
    J Clin Endocrinol Metab; 1988 Jul; 67(1):154-60. PubMed ID: 2837498
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adrenocorticotropin stimulation test in congenital adrenal hyperplasia: comparison between standard and low dose test.
    Panamonta O; Thinkhamrop B; Kirdpon W; Pudtawaro LO; Sungsahachart D
    J Med Assoc Thai; 2003 Jul; 86(7):634-40. PubMed ID: 12948258
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.
    Dumić M; Brkljacić L; Mardesić D; Plavsić V; Lukenda M; Kastelan A
    Acta Endocrinol (Copenh); 1985 Jul; 109(3):386-92. PubMed ID: 2992207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incidental adrenal nodules: association with exaggerated 17-hydroxyprogesterone response to adrenocorticotropic hormone.
    Turton DB; O'Brian JT; Shakir KM
    J Endocrinol Invest; 1992 Dec; 15(11):789-96. PubMed ID: 1337905
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A contribution to the classification of cases of non-classic 21-hydroxylase-deficient congenital adrenal hyperplasia.
    Phocas I; Chryssikopoulos A; Sarandakou A; Rizos D; Trakakis E
    Gynecol Endocrinol; 1995 Sep; 9(3):229-38. PubMed ID: 8540293
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S; Pollack MS; Loo M; Green O; Nussbaum R; Clayton G; Dupont B; New MI
    J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New reliable biochemical marker for screening 21 alpha-hydroxylase deficiency without index person among hirsute women in agreement with HLA-haplotyping.
    Chryssikopoulos A; Phocas I; Sarandakou A; Trakakis E; Rizos D
    J Endocrinol Invest; 1995 Nov; 18(10):754-61. PubMed ID: 8787951
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.
    Larizza D; Cuccia M; Martinetti M; Maghnie M; Dondi E; Salvaneschi L; Severi F
    Clin Endocrinol (Oxf); 1994 Jan; 40(1):39-45. PubMed ID: 8306479
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
    Stuckey MS; Boyne P; Macdonald WB; Christiansen FT; Houliston JB; Dawkins RL
    Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.