fludrocortisone has been researched along with Genetic Predisposition in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Çetin, T; Turan, İ | 1 |
| Aydinlioglu, H; Can, S; Guler, O; Kaya, A; Ozer, EA; Yildirimer, M | 1 |
| Gribouval, O; Gubler, MC; Landau, D; Schreiber, R; Shalev, H | 1 |
| Adams, JN; Bleyer, AJ; Cornell, LD; Elleder, M; Hart, PS; Hart, TC; Haws, R; Hodanová, K; Hulková, H; Kapp, K; Kmoch, S; Sikora, J; Sovová, J; Vyletal, P; Zivná, M; Zivný, J | 1 |
| Earle, NM; González, BR; Jiménez-Cohl, P; Thieck, EJ | 1 |
| Brändle, M; Kehl, O; Lipowsky, C; Schorl-Schweikardt, BA | 1 |
6 other study(ies) available for fludrocortisone and Genetic Predisposition
| Article | Year |
|---|---|
Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Female; Fludrocortisone; Genetic Predisposition to Disease; Genetic Variation; Humans; Hydrocortisone; Hypokalemic Periodic Paralysis; NAV1.4 Voltage-Gated Sodium Channel; Phenotype; Risk Factors; Steroid 21-Hydroxylase; Treatment Outcome | 2021 |
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 |
Inherited renal tubular dysgenesis may not be universally fatal.
Topics: Anuria; Child, Preschool; Female; Fludrocortisone; Genetic Predisposition to Disease; Heredity; Humans; Hyperkalemia; Hypotension; Kidney Tubules, Proximal; Male; Mutation; Oligohydramnios; Peptidyl-Dipeptidase A; Peritoneal Dialysis; Phenotype; Pregnancy; Treatment Outcome; Urogenital Abnormalities | 2010 |
Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.
Topics: Adult; Amino Acid Sequence; Anemia; Base Sequence; Biopsy; Blood Pressure; Cell Line; Child; Chronic Disease; Chymosin; Cytoplasm; DNA Mutational Analysis; Endoplasmic Reticulum; Enzyme Precursors; Female; Fludrocortisone; Genes, Dominant; Genetic Predisposition to Disease; Glomerular Filtration Rate; Glycosylation; Heterozygote; Humans; Hyperuricemia; Hypoaldosteronism; Kidney Concentrating Ability; Kidney Diseases; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polyuria; Protein Processing, Post-Translational; Protein Sorting Signals; Protein Transport; Renin; Transfection; Treatment Outcome | 2010 |
[Postural orthostatic tachycardia syndrome (POTS): report of 15 cases].
Topics: Adolescent; Adult; Cardiovascular Agents; Case-Control Studies; Child; Female; Fludrocortisone; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Postural Orthostatic Tachycardia Syndrome; Retrospective Studies; Syncope, Vasovagal; Tilt-Table Test; Treatment Outcome; Young Adult | 2012 |
[19-year-old patient with adrenal cortex insufficiency--only the tip of the iceberg. Polyendocrine autoimmune syndrome type II (Schmidt syndrome)].
Topics: Addison Disease; Adrenocorticotropic Hormone; Adult; Cortisone; Diagnosis, Differential; Drug Therapy, Combination; Fatigue; Female; Fludrocortisone; Genetic Predisposition to Disease; Humans; Hydrocortisone; Muscle Weakness; Polyendocrinopathies, Autoimmune; Thyroiditis, Autoimmune; Thyroxine; Weight Loss | 2008 |