aldosterone has been researched along with Orphan Diseases in 3 studies
Orphan Diseases: Rare diseases that have not been well studied.
Excerpt | Relevance | Reference |
---|---|---|
"Pseudohypoaldosteronism type I is a rare genetic disease of mineralocorticoid resistance that typically manifests in neonatal age." | 1.56 | Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease. ( de Potzolli, B; Seeliger, S; Tropschuh, A, 2020) |
"Bartter syndrome is an autosomal recessive renal tubulopathy that presents with hypokalemic, hypochloremic metabolic alkalosis associated with increased urinary loss of sodium, potassium, calcium and chloride." | 1.42 | A Rare Disorder with Common Clinical Presentation: Neonatal Bartter Syndrome. ( Al-Muhaizae, M; Hussain, S; Tarar, SH, 2015) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Tropschuh, A | 1 |
de Potzolli, B | 1 |
Seeliger, S | 1 |
Hussain, S | 1 |
Tarar, SH | 1 |
Al-Muhaizae, M | 1 |
LUISI, M | 1 |
SAVI, C | 1 |
COLI, F | 1 |
PANICUCCI, F | 1 |
MARESCOTTI, V | 1 |
3 other studies available for aldosterone and Orphan Diseases
Article | Year |
---|---|
Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease.
Topics: Adult; Aldosterone; Child, Preschool; Diagnosis, Differential; Failure to Thrive; Humans; Hyperkalem | 2020 |
A Rare Disorder with Common Clinical Presentation: Neonatal Bartter Syndrome.
Topics: Aldosterone; Anti-Inflammatory Agents, Non-Steroidal; Bartter Syndrome; Biomarkers; Humans; Indometh | 2015 |
[ANALYSIS OF CORTICOIDS BY MEANS OF THIN LAYER CHROMATOGRAPHY. I. QUALITIATIVE AND QUANTITATIVE SEPARATION OF PURE CORTICOID MIXTURES].
Topics: Adrenal Cortex Hormones; Aldosterone; Chromatography; Chromatography, Thin Layer; Corticosterone; Co | 1963 |