prednisolone has been researched along with Lipid Metabolism, Inborn Error in 3 studies
Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.
| Excerpt | Relevance | Reference |
|---|---|---|
| " It is concluded that there was a significant clinical and neurophysiologic response to prednisone at a dosage > or = 0." | 1.29 | Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone. ( Donner, EJ; Hale, DE; Murphy, EG; Tein, I, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ku, E | 1 |
| Thomas, M | 1 |
| Ho, CH | 1 |
| Whipple, NS | 1 |
| Abdul-Rahman, O | 1 |
| Megason, GC | 1 |
| Herrington, BL | 1 |
| Carmody, JB | 1 |
| Charlton, JR | 1 |
| Taube, KM | 1 |
| Beyer, C | 1 |
| Wozniak, KD | 1 |
| Tein, I | 1 |
| Donner, EJ | 1 |
| Hale, DE | 1 |
| Murphy, EG | 1 |
3 other studies available for prednisolone and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Index of suspicion. Case 1: fever, diarrhea, jaundice, and confusion in an 18-year-old male. Case 2: severe anemia in a 6-month-old girl. Case 3: red urine in a 4-month-old boy.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Anemia; Anti-Inflammatory Agents; Confusion; Congeni | 2014 |
[Importance of lipid metabolism in dermatology].
Topics: Cholesterol; Female; Humans; Hyperlipidemias; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Mal | 1981 |
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Administration, Oral; Child; Dose-Response Relationship, Drug; Fol | 1995 |