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Quoted phrase not found in phrase index: "Increased urinary 11-deoxycortisol level"
Page 1
Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
Kamrath C, Hartmann MF, Boettcher C, Wudy SA. Kamrath C, et al. J Pediatr. 2014 Aug;165(2):280-4. doi: 10.1016/j.jpeds.2014.04.011. Epub 2014 May 23. J Pediatr. 2014. PMID: 24862381
OBJECTIVE: To characterize the urinary steroid metabolome of neonates and infants born either at term or preterm. ...Our analysis clarifies, first, why preterms have higher 17OHP levels and thus higher rates of false-positive screening results for congenital adrenal …
OBJECTIVE: To characterize the urinary steroid metabolome of neonates and infants born either at term or preterm. ...Our analysis cla …
Licorice - or more?
Leitolf H, Dixit KC, Higham CE, Brabant G. Leitolf H, et al. Exp Clin Endocrinol Diabetes. 2010 Apr;118(4):250-3. doi: 10.1055/s-0029-1224123. Epub 2010 Mar 8. Exp Clin Endocrinol Diabetes. 2010. PMID: 20213599
Morning ambulant aldosterone was slightly increased at 801 pmol/L and renin activity was undetectable. Urinary 24 h aldosterone excretion was significantly increased at 162 ng/24 h with normal cortisol and catecholamine excretion. ...Testosterone level
Morning ambulant aldosterone was slightly increased at 801 pmol/L and renin activity was undetectable. Urinary 24 h aldosteron …
11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
Rösler A, Weshler N, Leiberman E, Hochberg Z, Weidenfeld J, Sack J, Chemke J. Rösler A, et al. J Clin Endocrinol Metab. 1988 Apr;66(4):830-8. doi: 10.1210/jcem-66-4-830. J Clin Endocrinol Metab. 1988. PMID: 3346360
AF THS and 11-deoxycortisol concentrations were markedly elevated in pregnancies with affected fetuses (P less than 0.01), but normal in nonaffected ones. ...AF 17-hydroxyprogesterone, testosterone, and 11-deoxycorticosterone levels were normal in all pregnan …
AF THS and 11-deoxycortisol concentrations were markedly elevated in pregnancies with affected fetuses (P less than 0.01), but …
Urinary steroid profile in adrenocortical tumors.
Kikuchi E, Yanaihara H, Nakashima J, Homma K, Ohigashi T, Asakura H, Tachibana M, Shibata H, Saruta T, Murai M. Kikuchi E, et al. Biomed Pharmacother. 2000 Jun;54 Suppl 1:194s-197s. doi: 10.1016/s0753-3322(00)80043-8. Biomed Pharmacother. 2000. PMID: 10915023 Clinical Trial.
Patients with adrenal adenomas from primary hyperaldosteronism had increased metabolites of 18-hydroxycorticosterone and aldosterone, and those with Cushing's syndrome had elevated excretion of 11 -deoxycortisol, cortisol, 18-hydroxycortisol, and cortisone me …
Patients with adrenal adenomas from primary hyperaldosteronism had increased metabolites of 18-hydroxycorticosterone and aldosterone, …
Plasma 11-deoxycortisol, androstenedione, testosterone and ACTH in comparison with the urinary excretion of tetrahydro-11-deoxycortisol as indices of the pituitary-adrenal response to oral metyrapone.
de Lange WE, Sluiter WJ, Pratt JJ, Doorenbos H. de Lange WE, et al. Acta Endocrinol (Copenh). 1980 Apr;93(4):488-94. doi: 10.1530/acta.0.0930488. Acta Endocrinol (Copenh). 1980. PMID: 6247869
Plasma levels of ACTH, 11-deoxycortisol, androstenedione and testosterone and urinary tetrahydro-11-deoxycortisol were determined during a two day oral metyrapone test using doses of 1.5 g every 6 h. ...The rise of androstenedione concent …
Plasma levels of ACTH, 11-deoxycortisol, androstenedione and testosterone and urinary tetrahydro-11-de
Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine.
Hughes IA, Arisaka O, Perry LA, Honour JW. Hughes IA, et al. Acta Endocrinol (Copenh). 1986 Mar;111(3):349-54. doi: 10.1530/acta.0.1110349. Acta Endocrinol (Copenh). 1986. PMID: 3515819
Plasma renin activity was suppressed, but increased to levels characteristic of infancy within 4 weeks of treatment. The enzyme defect was confirmed by measurement of increased urinary excretion of tetrahydro-11-deoxycortisol. A more pola …
Plasma renin activity was suppressed, but increased to levels characteristic of infancy within 4 weeks of treatment. The enzym …
Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.
Lobo RA, Goebelsmann U. Lobo RA, et al. Am J Obstet Gynecol. 1980 Nov 15;138(6):720-6. doi: 10.1016/0002-9378(80)90095-2. Am J Obstet Gynecol. 1980. PMID: 6254362
The five CAH patients had decreased cortisol but normal 11-deoxycortisol responses to ACTH, thus indicating 21-hydroxylase deficiency (21HD). ...The diagnosis of it hinges upon the post-ACTH rise in 17OHP, whereas the levels of serum androgens and urinary
The five CAH patients had decreased cortisol but normal 11-deoxycortisol responses to ACTH, thus indicating 21-hydroxylase def …
Steroid profile in serum: increased levels of sulphated pregnenolone and pregn-5-ene-3 beta,20 alpha-diol in patients with adrenocortical carcinoma.
Gröndal S, Curstedt T. Gröndal S, et al. Acta Endocrinol (Copenh). 1991 Apr;124(4):381-5. doi: 10.1530/acta.0.1240381. Acta Endocrinol (Copenh). 1991. PMID: 2031435
Serum levels of 11-deoxycortisol and/or its glucuronated metabolite tetrahydro-11-deoxycortisol were clearly elevated in 8 of the patients with carcinoma. ...The serum levels of sulphated pregnenolone and/or pregn-5-ene-3 beta,20 alpha-di …
Serum levels of 11-deoxycortisol and/or its glucuronated metabolite tetrahydro-11-deoxycortisol were clea …
Steroid profile in urine: a useful tool in the diagnosis and follow up of adrenocortical carcinoma.
Gröndal S, Eriksson B, Hagenäs L, Werner S, Curstedt T. Gröndal S, et al. Acta Endocrinol (Copenh). 1990 May;122(5):656-63. doi: 10.1530/acta.0.1220656. Acta Endocrinol (Copenh). 1990. PMID: 2141212
The steroid profile varied widely between the patients with adrenocortical carcinoma. Patients with Cushing's syndrome had increased levels of cortisol metabolites and those with virilism had raised excretion of androgen metabolites. ...In 23 of the 24 patients the …
The steroid profile varied widely between the patients with adrenocortical carcinoma. Patients with Cushing's syndrome had increased
Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A. Hurwitz A, et al. J Clin Endocrinol Metab. 1985 Apr;60(4):631-8. doi: 10.1210/jcem-60-4-631. J Clin Endocrinol Metab. 1985. PMID: 2982904
PRA was elevated in three patients, while urinary aldosterone was normal or increased. 11 beta-Hydroxylase deficiency was diagnosed on the basis of increased 11-deoxycortisol and deoxycorticosterone in plasma and tetrahydro-11-deoxycor
PRA was elevated in three patients, while urinary aldosterone was normal or increased. 11 beta-Hydroxylase deficiency was diag …
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