fludrocortisone has been researched along with 46, XX Disorders of Sex Development in 2 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 | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Akdoğan, MP; Aycan, Z; Bayramoğlu, E; Çetinkaya, S; Erdeve, ŞŞ; Karaman, A; Şahin, NM | 1 |
Birla, S; Jain, R; Jain, V; Sharma, A; Verma, N | 1 |
2 other study(ies) available for fludrocortisone and 46, XX Disorders of Sex Development
Article | Year |
---|---|
Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency.
Topics: 46, XX Disorders of Sex Development; Adrenal Hyperplasia, Congenital; Amino Acid Substitution; Anti-Inflammatory Agents; Drug Therapy, Combination; Female; Fludrocortisone; Gonadotropins; Homozygote; Humans; Hydrocortisone; Infant, Newborn; Mutation; Ovarian Cysts; Ovary; Steroid 21-Hydroxylase; Treatment Outcome; Tumor Burden; Uterine Hemorrhage | 2018 |
Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
Topics: 46, XX Disorders of Sex Development; Adolescent; Adrenal Hyperplasia, Congenital; Aromatase; Bone Density; Child Development; Child, Preschool; DNA Mutational Analysis; Estrogen Replacement Therapy; Ethinyl Estradiol; Female; Fludrocortisone; Growth Disorders; Gynecomastia; Humans; Hydrocortisone; Infertility, Male; Insulin Resistance; Male; Metabolism, Inborn Errors; Mutation, Missense; Pedigree; Sexual Maturation | 2012 |