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)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hsiao, PH; Lee, CT; Lee, JS; Tsai, WY; Tung, YC1
Cawood, M; Ismail, AA; Jones, ST; Ufodiama, EB1
Frank, GR; Kreitzer, PM; Yoon, DY1
Nadel, FM; Weinzimer, SA1
Binder, G; Iliev, DI; Leriche, C; Petruch, UR; Ranke, MB; Strotbek, G; Wollmann, HA1
Achermann, JC; Habiby, RL; Ito, M; Jameson, JL; Pang, S; Rosler, A; Silverman, BL1

Reviews

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

ArticleYear
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

ArticleYear
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