17-alpha-hydroxyprogesterone has been researched along with Turner Syndrome in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (28.57) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 2 (28.57) | 2.80 |
Authors | Studies |
---|---|
Han, M; Liang, D; Liu, Y; Ren, Y; Xu, L; Yang, J; Yin, J; Zhang, Y | 1 |
Beltrán, LJ; Burgos, G; Cueva-Ludeña, K; Dueñas-Espín, I; Espín, E; Espinosa-Herrera, F; Gómez-Correa, D; Llamos, A; Pinto-Basto, J; Rojas, S; Salazar-Vega, J; Tito-Álvarez, AM; Zurita, C | 1 |
Agladioglu, SY; Aycan, Z; Bas, VN; Cetinkaya, S; Kendirci, HN; Onder, A | 1 |
Cuccia, M; Dondi, E; Larizza, D; Maghnie, M; Martinetti, M; Salvaneschi, L; Severi, F | 1 |
Balducci, R; Boscherini, B; Di Rito, A; Galasso, C; Larizza, D; Mangiantini, A; Municchi, G; Picone, S; Toscano, V | 1 |
Dvorakova, M; Hampl, R; Hill, M; Lebl, J; Lisa, L; Snajderova, M; Starka, L; Sulcova, J | 1 |
Bragliani, M; Cisternino, M; Cuccia, M; Dondi, E; Larizza, D; Mantovani, V; Martinetti, M; Viggiani, M | 1 |
1 trial(s) available for 17-alpha-hydroxyprogesterone and Turner Syndrome
Article | Year |
---|---|
Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Child; Child, Preschool; Diagnostic Techniques, Endocrine; DNA Mutational Analysis; Female; Humans; Hydrocortisone; Incidence; Steroid 21-Hydroxylase; Turner Syndrome; Young Adult | 2012 |
6 other study(ies) available for 17-alpha-hydroxyprogesterone and Turner Syndrome
Article | Year |
---|---|
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Hyperplasia, Congenital; Adult; Chromosome Aberrations; Female; Graves Disease; Humans; Prednisone; Steroid 21-Hydroxylase; Testosterone; Turner Syndrome; Young Adult | 2022 |
A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Amenorrhea; Consanguinity; Dehydroepiandrosterone Sulfate; Desoxycorticosterone; Diagnostic Errors; Ecuador; Female; Homozygote; Humans; Hydrocortisone; Hypertension; Hypogonadism; Hypokalemia; Mosaicism; Osteoporosis; Siblings; Steroid 17-alpha-Hydroxylase; Turner Syndrome; Young Adult | 2020 |
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Adult; Child; Child, Preschool; Family; Female; Heterozygote; HLA Antigens; HLA-B Antigens; HLA-B14 Antigen; HLA-B35 Antigen; HLA-B8 Antigen; Humans; Hydroxyprogesterones; Incidence; Male; Pedigree; Polymorphism, Genetic; Stimulation, Chemical; Turner Syndrome | 1994 |
Effects of long-term growth hormone therapy on adrenal steroidogenesis in Turner syndrome.
Topics: 17-alpha-Hydroxypregnenolone; 17-alpha-Hydroxyprogesterone; Adrenal Cortex Hormones; Androstenedione; Child; Child, Preschool; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Female; Human Growth Hormone; Humans; Hydrocortisone; Insulin-Like Growth Factor I; Time Factors; Turner Syndrome | 1998 |
Sex hormone-binding globulin as a marker of the effect of hormonal treatment in Turner's syndrome.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Cortex Hormones; Adult; Androstenedione; Biomarkers; Child; Child, Preschool; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Estradiol; Estrogens; Female; Human Growth Hormone; Humans; Immunoradiometric Assay; Insulin-Like Growth Factor I; Medroxyprogesterone Acetate; Progesterone; Sex Hormone-Binding Globulin; Testosterone; Turner Syndrome | 2001 |
Do reduced levels of steroid 21-hydroxylase confer a survival advantage in fetuses affected by sex chromosome aberrations?
Topics: 17-alpha-Hydroxyprogesterone; Adrenocorticotropic Hormone; Female; Fetal Viability; Fetus; Humans; Klinefelter Syndrome; Male; Mutation; Sex Chromosome Aberrations; Steroid 21-Hydroxylase; Turner Syndrome | 2002 |