tetrahydrocortisone has been researched along with Adrenal Hyperplasia, Congenital in 10 studies
Adrenal Hyperplasia, Congenital: A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (60.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kamrath, C | 1 |
| Hartmann, MF | 1 |
| Boettcher, C | 1 |
| Zimmer, KP | 1 |
| Wudy, SA | 1 |
| Koyama, Y | 1 |
| Homma, K | 1 |
| Fukami, M | 1 |
| Miwa, M | 1 |
| Ikeda, K | 1 |
| Ogata, T | 1 |
| Hasegawa, T | 1 |
| Murata, M | 1 |
| Taylor, NF | 1 |
| Chan, AO | 1 |
| BAYLISS, RI | 1 |
| BROADBENT, IE | 1 |
| STEINBECK, AW | 1 |
| DECOURT, J | 1 |
| MICHARD, JP | 1 |
| BAULIEU, E | 1 |
| TOURNEUR, R | 1 |
| LOUCHART, J | 1 |
| LEVEAU, J | 1 |
| van der Ploeg, KR | 1 |
| Wolthers, BG | 1 |
| Nagel, GT | 1 |
| Volmer, M | 1 |
| Drayer, NM | 1 |
| Rösler, A | 2 |
| Leiberman, E | 2 |
| Rosenmann, A | 1 |
| Ben-Uzilio, R | 1 |
| Weidenfeld, J | 2 |
| Zachmann, M | 1 |
| Kempken, B | 1 |
| Manella, B | 1 |
| Navarro, E | 1 |
| Weshler, N | 1 |
| Hochberg, Z | 1 |
| Sack, J | 1 |
| Chemke, J | 1 |
| Vierhapper, H | 1 |
| Nowotny, P | 1 |
| Waldhäusl, W | 1 |
| Frisch, H | 1 |
10 other studies available for tetrahydrocortisone and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography-mass spectrometry analysis: Reference values for neonates and infants.
Topics: Adrenal Hyperplasia, Congenital; Cohort Studies; Female; Gas Chromatography-Mass Spectrometry; Human | 2016 |
Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androsterone; Biomarkers; Case-Contro | 2012 |
New strategies for detecting steroid metabolic disorders--paneling vs profiling.
Topics: Adrenal Hyperplasia, Congenital; Androsterone; Female; Humans; Male; NADPH-Ferrihemoprotein Reductas | 2012 |
Congenital adrenal hyperplasia; effects of corticotrophin and tetrahydrocortisone.
Topics: Adrenal Cortex; Adrenal Cortex Diseases; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormon | 1954 |
[Congenital adrenal hyperplasia of the pseudohermaphroditic type; attempts at inhibition by tetrahydrocortisone and fludrocortisone].
Topics: Adrenal Hyperplasia, Congenital; Adrenogenital Syndrome; Disorders of Sex Development; Fludrocortiso | 1956 |
The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.
Topics: Adrenal Hyperplasia, Congenital; Aging; Androstanes; Chromatography, Gas; Female; Gas Chromatography | 1982 |
Prenatal diagnosis of 11beta-hydroxylase deficiency congenital adrenal hyperplasia.
Topics: Adrenal Hyperplasia, Congenital; Amniotic Fluid; Female; Gestational Age; Humans; Male; Pregnancy; P | 1979 |
Conversion from pure 17,20-desmolase- to combined 17,20-desmolase/17 alpha-hydroxylase deficiency with age.
Topics: Adrenal Hyperplasia, Congenital; Adult; Aging; Aldehyde-Lyases; Blood Pressure; Cytochrome P-450 Enz | 1992 |
11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
Topics: Adrenal Hyperplasia, Congenital; Adult; Amniotic Fluid; Cortodoxone; Female; Fetal Diseases; Humans; | 1988 |
Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adult; Child; Child, Preschool; Chromatography, Gas; Fe | 1985 |