clonidine has been researched along with Nephritis, Hereditary in 1 studies
Clonidine: An imidazoline sympatholytic agent that stimulates ALPHA-2 ADRENERGIC RECEPTORS and central IMIDAZOLINE RECEPTORS. It is commonly used in the management of HYPERTENSION.
clonidine (amino form) : A clonidine that is 4,5-dihydro-1H-imidazol-2-amine in which one of the amino hydrogens is replaced by a 2,6-dichlorophenyl group.
Nephritis, Hereditary: A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Even when drug-resistance appears to be responsible for the failure to control secondary hypertension in AS, clonidine may represent a safe, effective option in the normalization of high blood pressure." | 3.76 | Ventricular septal defect in a child with Alport syndrome: a case report. ( Bassareo, PP; Marras, AR; Mercuro, G, 2010) |
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bassareo, PP | 1 |
| Marras, AR | 1 |
| Mercuro, G | 1 |
1 other study available for clonidine and Nephritis, Hereditary
| Article | Year |
|---|---|
Ventricular septal defect in a child with Alport syndrome: a case report.
Topics: Adrenergic alpha-2 Receptor Agonists; Antihypertensive Agents; Clonidine; Collagen Type IV; Disease | 2010 |