17-alpha-hydroxypregnenolone has been researched along with Orphan Diseases in 1 studies
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Araújo, VG; Cruz, CB; Gameleira, KP; Lofrano-Porto, A; Oliveira, RS | 1 |
1 other study(ies) available for 17-alpha-hydroxypregnenolone and Orphan Diseases
| Article | Year |
|---|---|
3β-hydroxysteroid dehydrogenase type II deficiency on newborn screening test.
Topics: 17-alpha-Hydroxypregnenolone; Adrenal Hyperplasia, Congenital; Disorders of Sex Development; Homozygote; Humans; Infant, Newborn; Male; Mutation; Neonatal Screening; Progesterone Reductase; Rare Diseases | 2014 |