17-alpha-hydroxyprogesterone has been researched along with 46, XY Disorders of Sex Development 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 |
|---|---|
| Kim, GH; Koh, JW; Yoo, HW; Yu, J | 1 |
| Bahíllo-Curieses, MP; del Cañizo López, A; Loidi Fernández de Trocóniz, L; Martínez-Sopena, MJ | 1 |
| Balogh, E; Jakab, J; Kiss, A; Kovács, J; Ladányi, E; Megyeri, T; Papp, J; Ságodi, L; Ujfalusi, A | 1 |
3 other study(ies) available for 17-alpha-hydroxyprogesterone and 46, XY Disorders of Sex Development
| Article | Year |
|---|---|
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 |
[Partial 3ß-hydroxysteroid dehydrogenase type 2 deficiency: Diagnosis of a novel mutation after positive newborn screening for 21-hydroxylase deficiency].
Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Chorionic Gonadotropin; Diagnostic Errors; Disorder of Sex Development, 46,XY; Heterozygote; Hormones; Humans; Infant, Newborn; Male; Mutation, Missense; Neonatal Screening; Point Mutation; Progesterone Reductase; Testis; Testosterone | 2016 |
[Dysgenetic male pseudohermaphroditism].
Topics: 17-alpha-Hydroxyprogesterone; Androstenedione; Biomarkers; Chromosomes, Human, X; Chromosomes, Human, Y; Diagnosis, Differential; Disorder of Sex Development, 46,XY; Disorders of Sex Development; Follicle Stimulating Hormone; Humans; Hypospadias; In Situ Hybridization, Fluorescence; Infant, Newborn; Luteinizing Hormone; Male; Mosaicism; Testis; Testosterone | 2012 |