17-alpha-hydroxyprogesterone has been researched along with pregnanetriolone in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hikita, Y | 1 |
| Hasegawa, T; Homma, K; Ito, T; Mizuno, H; Ohro, Y; Ono, M; Sugiyama, Y; Togari, H; Ueshiba, H | 1 |
| Anzo, M; Hamajima, T; Hasegawa, T; Homma, K; Jinno, K; Matsuo, N; Ohashi, T; Takahashi, T; Takahashi, Y; Takeshita, E; Toyoura, T; Watanabe, K | 1 |
| Fukami, M; Hasegawa, T; Homma, K; Ikeda, K; Koyama, Y; Miwa, M; Murata, M; Ogata, T | 1 |
| Fukami, M; Hasegawa, T; Hayashi, M; Homma, K; Kataoka, Y; Kato, F; Ogata, T; Oiso, Y; Sasano, H; Sugimura, Y; Tanaka, H | 1 |
| Boettcher, C; Hartmann, MF; Kamrath, C; Wudy, SA | 1 |
6 other study(ies) available for 17-alpha-hydroxyprogesterone and pregnanetriolone
| Article | Year |
|---|---|
[Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography].
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Chromatography, Gas; Cortodoxone; Female; Follow-Up Studies; Humans; Hydroxyprogesterones; Male; Mass Screening; Pregnancy; Pregnanetriol; Steroid Hydroxylases | 1985 |
Transient hyper-17-OHPnemia unrelated to cross-reactions with residual fetal adrenal cortex products.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Cortex; Adrenocorticotropic Hormone; Aging; Chromatography, High Pressure Liquid; Cross Reactions; Fetus; Humans; Infant, Newborn; Male; Polymerase Chain Reaction; Pregnanetriol; Radioimmunoassay; Steroid 21-Hydroxylase; Time Factors | 2004 |
Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Case-Control Studies; Diagnosis, Differential; Female; Gestational Age; Humans; Infant, Newborn; Infant, Premature; Male; Pregnanetriol; Sensitivity and Specificity | 2004 |
Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androsterone; Biomarkers; Case-Control Studies; Diagnosis, Differential; Female; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Male; NADPH-Ferrihemoprotein Reductase; Pregnanetriol; Steroid 17-alpha-Hydroxylase; Steroid 21-Hydroxylase; Tetrahydrocortisone | 2012 |
A 68-year-old phenotypically male patient with 21-hydroxylase deficiency and concomitant adrenocortical neoplasm producing testosterone and cortisol.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Cortex Neoplasms; Adrenal Hyperplasia, Congenital; Aged; Androstenedione; Base Sequence; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydrocortisone; Immunohistochemistry; Japan; Magnetic Resonance Imaging; Male; Molecular Sequence Data; Pregnanetriol; Sequence Analysis, DNA; Testosterone | 2013 |
Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Chromatography, Gas; Cortodoxone; Female; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Infant, Premature; Male; Mass Spectrometry; Metabolome; Pregnanetriol; Retrospective Studies; Steroid 11-beta-Hydroxylase; Steroid 17-alpha-Hydroxylase | 2014 |