17-alpha-hydroxyprogesterone has been researched along with Deficiency, Mental in 2 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 | 2 (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 |
2 other study(ies) available for 17-alpha-hydroxyprogesterone and Deficiency, Mental
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 |