fludrocortisone has been researched along with Genetic Diseases, X-Chromosome Linked in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aydinlioglu, H; Can, S; Guler, O; Kaya, A; Ozer, EA; Yildirimer, M | 1 |
| Hanaki, K; Kanzaki, S; Kawashima, Y; Kinoshita, T; Nagaishi, J; Yang, F | 1 |
| Fernández García, R; García García, E; Madruga Garrido, M; Martínez Ortega, AJ | 1 |
3 other study(ies) available for fludrocortisone and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
A novel DAX1 gene mutation in a Turkish infant with X-linked adrenal hypoplasia congenita.
Topics: Adrenal Insufficiency; Base Sequence; Codon, Terminator; DAX-1 Orphan Nuclear Receptor; DNA-Binding Proteins; Fludrocortisone; Genetic Diseases, X-Linked; Genetic Predisposition to Disease; Heterozygote; Hormones; Humans; Hydrocortisone; Hypogonadism; Infant, Newborn; Male; Mutation; Pedigree; Receptors, Retinoic Acid; Repressor Proteins; Sequence Deletion | 2009 |
Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene.
Topics: Adrenal Insufficiency; Child; Codon, Terminator; DAX-1 Orphan Nuclear Receptor; DNA-Binding Proteins; Fludrocortisone; Genetic Diseases, X-Linked; Hormones; Humans; Hydrocortisone; Hypogonadism; Male; Mutation; Receptors, Retinoic Acid; Repressor Proteins | 2009 |
[Congenital adrenal hypoplasia as the first manifestation of a contiguous deletion of genes in Xp21].
Topics: Adrenal Cortex Hormones; Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Carbohydrate Metabolism, Inborn Errors; Chromosome Deletion; Chromosomes, Human, X; Creatine Kinase, MM Form; DAX-1 Orphan Nuclear Receptor; Dystrophin; Female; Fludrocortisone; Genes, X-Linked; Genetic Counseling; Genetic Diseases, X-Linked; Glycerol Kinase; Gonadal Steroid Hormones; Heterozygote; Humans; Hydrocortisone; Hypertriglyceridemia; Hypoadrenocorticism, Familial; Infant, Newborn; Interleukin-1 Receptor Accessory Protein; Male; Mental Retardation, X-Linked; Muscular Dystrophy, Duchenne; Sequence Deletion; Syndrome | 2013 |