17-alpha-hydroxyprogesterone has been researched along with Genetic Diseases, X-Chromosome Linked in 3 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 | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bertini, ES; Biagini, G; Cusmai, R; Gecz, J; Giannone, G; Lucchi, C; Rustichelli, C; Specchio, N; Terracciano, A; Trivisano, M; Ubertini, GM; Vigevano, F | 1 |
| Kim, GH; Koh, JW; Yoo, HW; Yu, J | 1 |
| Ali, JM; Harun, F; Jalaludin, MY | 1 |
3 other study(ies) available for 17-alpha-hydroxyprogesterone and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Reduced steroidogenesis in patients with PCDH19-female limited epilepsy.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenocorticotropic Hormone; Adrenogenital Syndrome; Cadherins; Case-Control Studies; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy; Estradiol; Female; Genetic Diseases, X-Linked; Gonadal Steroid Hormones; Humans; Hydrocortisone; Intellectual Disability; Pregnanolone; Pregnenolone; Progesterone; Prospective Studies; Protocadherins; Puberty, Precocious; Reference Values | 2017 |
Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Adrenocorticotropic Hormone; Bone Development; Child; Child, Preschool; DAX-1 Orphan Nuclear Receptor; Disorder of Sex Development, 46,XY; Female; Genetic Diseases, X-Linked; Genotype; Glucocorticoids; Humans; Hypoadrenocorticism, Familial; Intellectual Disability; Male; Mineralocorticoids; Obesity; Phosphoproteins; Puberty, Precocious; Retrospective Studies; Steroid 21-Hydroxylase | 2013 |
Late onset X-linked adrenal hypoplasia congenita with hypogonadotropic hypgonadism due to a novel 4-bp deletion in exon 2 of NR0B1.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Age of Onset; Child; DAX-1 Orphan Nuclear Receptor; Exons; Genetic Diseases, X-Linked; Humans; Hypoadrenocorticism, Familial; Hypogonadism; Male; Mutation; Pedigree; Prognosis; Sequence Deletion | 2014 |