fludrocortisone has been researched along with Hypogonadism in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Chaveeva, P; Milcheva, R; Staynova, R; Yanachkova, V | 1 |
| 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 |
| Abalain, JH; Bercovici, JP; Fiet, J; Floch, HH; Fournier, G; Gibault, L; Sonnet, E; Volant, A | 1 |
| Gardner, DF; Watlington, CO | 1 |
| Blichfeldt, S; Müller, J; Schwartz, M | 1 |
6 other study(ies) available for fludrocortisone and Hypogonadism
| Article | Year |
|---|---|
Autoimmune Polyglandular Syndrome Type 2 and Pregnancy.
Topics: Acute Disease; Addison Disease; Adult; Blood Glucose; Cesarean Section; Disease Management; Electrocardiography; Female; Fertilization in Vitro; Fludrocortisone; Glucocorticoids; Hashimoto Disease; Hormone Replacement Therapy; Humans; Hypogonadism; Mineralocorticoids; Polyendocrinopathies, Autoimmune; Prednisolone; Pregnancy; Pregnancy Complications; Thyrotropin; Thyroxine; Water-Electrolyte Imbalance | 2020 |
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 |
Testicular adrenal rest tumours in salt wasting congenital adrenal hyperplasia (in vivo and in vitro studies).
Topics: Adrenal Hyperplasia, Congenital; Adrenal Rest Tumor; Adrenocorticotropic Hormone; Adult; Dehydroepiandrosterone Sulfate; Dexamethasone; Diagnosis, Differential; Fludrocortisone; Follicle Stimulating Hormone; Follow-Up Studies; Glucocorticoids; Gonadotropin-Releasing Hormone; Humans; Hydrocortisone; Hypogonadism; Inhibins; Leydig Cell Tumor; Luteinizing Hormone; Male; Prolactin; Renin; Steroid 21-Hydroxylase; Testicular Neoplasms; Treatment Refusal; Ultrasonography | 2005 |
Sella turcica erosion and transient hypogonadism in the multiple endocrine deficiency syndrome.
Topics: Adult; Endocrine System Diseases; Fludrocortisone; Humans; Hydrocortisone; Hypogonadism; Hypothyroidism; Male; Radiography; Sella Turcica; Thyroxine | 1981 |
X-linked adrenal hypoplasia in a large Greenlandic family. Detection of a missense mutation (N4401) in the DAX-1 gene; implication for genetic counselling and carrier diagnosis.
Topics: Adolescent; Adrenal Insufficiency; Adult; Amino Acid Sequence; Base Sequence; Body Height; Child, Preschool; DAX-1 Orphan Nuclear Receptor; DNA Primers; DNA-Binding Proteins; Female; Fludrocortisone; Genetic Carrier Screening; Genetic Counseling; Greenland; Humans; Hydrocortisone; Hypogonadism; Infant; Male; Pedigree; Point Mutation; Polymerase Chain Reaction; Receptors, Retinoic Acid; Repressor Proteins; Testosterone; Transcription Factors; X Chromosome | 1997 |