flumazenil has been researched along with Adrenal Hyperplasia, Congenital in 2 studies
Flumazenil: A potent benzodiazepine receptor antagonist. Since it reverses the sedative and other actions of benzodiazepines, it has been suggested as an antidote to benzodiazepine overdoses.
flumazenil : An organic heterotricyclic compound that is 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted at positions 3, 5, 6, and 8 by ethoxycarbonyl, methyl, oxo, and fluoro groups, respectively. It is used as an antidote to benzodiazepine overdose.
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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dumic, KK | 1 |
| Grubic, Z | 1 |
| Kusec, V | 1 |
| Braovac, D | 1 |
| Gotovac, K | 1 |
| Vinkovic, M | 1 |
| Vucinic, M | 1 |
| Dumic, M | 1 |
| Kocova, M | 1 |
| Anastasovska, V | 1 |
| Petlichkovski, A | 1 |
| Falhammar, H | 1 |
2 other studies available for flumazenil and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population.
Topics: Adrenal Hyperplasia, Congenital; Croatia; Cross-Sectional Studies; Genotype; Humans; Prevalence; Rom | 2023 |
First insights into the genetics of 21-hydroxylase deficiency in the Roma population.
Topics: Adrenal Hyperplasia, Congenital; Genotype; Humans; Mutation; Roma; Steroid 21-Hydroxylase | 2021 |