androstenedione has been researched along with Hyponatremia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hsiao, PH; Lee, CT; Lee, JS; Tsai, WY; Tung, YC | 1 |
| Burke, CW | 1 |
1 review(s) available for androstenedione and Hyponatremia
| Article | Year |
|---|---|
Adrenocortical insufficiency.
Topics: Addison Disease; Adrenal Insufficiency; Adrenocorticotropic Hormone; Aldosterone; Androstenedione; Animals; Autoimmune Diseases; Blood Volume; Body Water; Calcium; Catecholamines; Cosyntropin; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Delayed-Action Preparations; Disease Models, Animal; Glomerular Filtration Rate; Glucocorticoids; Humans; Hypoglycemia; Hyponatremia; Hypotension; Hypothalamo-Hypophyseal System; Kidney; Posture; Prolactin; Regional Blood Flow; Skin Pigmentation; Thyroid Gland; Tomography, X-Ray Computed; Water-Electrolyte Balance | 1985 |
1 other study(ies) available for androstenedione and Hyponatremia
| Article | Year |
|---|---|
Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the pre-screening era.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androstenedione; Dehydroepiandrosterone; Female; Genotype; Humans; Hydrocortisone; Hyponatremia; Infant, Newborn; Male; Phenotype; Pigmentation Disorders; Point Mutation; Pregnancy; Steroid 21-Hydroxylase | 2010 |