Compounds > 17-alpha-hydroxyprogesterone

Page last updated: 2024-08-17

17-alpha-hydroxyprogesterone and Hyponatremia

17-alpha-hydroxyprogesterone has been researched along with Hyponatremia in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (16.67)	18.2507
2000's	4 (66.67)	29.6817
2010's	1 (16.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hsiao, PH; Lee, CT; Lee, JS; Tsai, WY; Tung, YC	1
Cawood, M; Ismail, AA; Jones, ST; Ufodiama, EB	1
Frank, GR; Kreitzer, PM; Yoon, DY	1
Nadel, FM; Weinzimer, SA	1
Binder, G; Iliev, DI; Leriche, C; Petruch, UR; Ranke, MB; Strotbek, G; Wollmann, HA	1
Achermann, JC; Habiby, RL; Ito, M; Jameson, JL; Pang, S; Rosler, A; Silverman, BL	1

Reviews

1 review(s) available for 17-alpha-hydroxyprogesterone and Hyponatremia

Article	Year
The case of the missing "olive". Pediatric annals, 2000, Volume: 29, Issue:2 Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Diagnosis, Differential; Humans; Hyperkalemia; Hyponatremia; Infant, Newborn; Male; Pyloric Stenosis; Vomiting	2000

Other Studies

5 other study(ies) available for 17-alpha-hydroxyprogesterone and Hyponatremia

Article	Year
Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the pre-screening era. Journal of the Formosan Medical Association = Taiwan yi zhi, 2010, Volume: 109, Issue:2 Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androstenedione; Dehydroepiandrosterone; Female; Genotype; Humans; Hydrocortisone; Hyponatremia; Infant, Newborn; Male; Phenotype; Pigmentation Disorders; Point Mutation; Pregnancy; Steroid 21-Hydroxylase	2010
Limitations of 17-hydroxyprogesterone in investigating neonatal hyponatraemia. Annals of clinical biochemistry, 2004, Volume: 41, Issue:Pt 3 Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Anti-Bacterial Agents; Biomarkers; Female; Humans; Hydrocortisone; Hyponatremia; Infant; Infant, Newborn; Jaundice, Neonatal; Male; Respiratory Tract Infections; Sodium Chloride; Steroids; Stimulation, Chemical	2004
Near-fatal misdiagnosis of congenital adrenal hyperplasia. The Journal of pediatrics, 1997, Volume: 131, Issue:1 Pt 1 Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Anti-Inflammatory Agents; Cortodoxone; Diagnostic Errors; Female; Humans; Hydrocortisone; Hyponatremia; Infant, Newborn; Laboratories; Renin	1997
Transient pseudohypoaldosteronism with complex malformation of internal genitalia. A case report. Hormone research, 2000, Volume: 54, Issue:3 Topics: 17-alpha-Hydroxyprogesterone; Adrenocorticotropic Hormone; Aldosterone; Antibiotic Prophylaxis; Dehydration; Female; Genitalia, Female; Gestational Age; Humans; Hyponatremia; Infant, Newborn; Kidney; Ovary; Potassium; Pseudohypoaldosteronism; Renin; Sodium; Ultrasonography; Uterus; Vagina	2000
Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression. The Journal of clinical endocrinology and metabolism, 2001, Volume: 86, Issue:7 Topics: 17-alpha-Hydroxyprogesterone; Adrenal Insufficiency; Adrenocorticotropic Hormone; Aldosterone; Cell Line; Cortodoxone; DAX-1 Orphan Nuclear Receptor; DNA-Binding Proteins; Embryo, Mammalian; Genetic Linkage; Humans; Hydrocortisone; Hyperkalemia; Hyponatremia; Infant; Infant, Newborn; Kidney; Male; Mutation, Missense; Receptors, Retinoic Acid; Renin; Repressor Proteins; Transcription Factors; Transcription, Genetic; X Chromosome	2001