prednisolone has been researched along with Central Nervous System Demyelinating Diseases, Hereditary 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.
| 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 | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Heidari, E | 1 |
| Rasoulinezhad, M | 1 |
| Pak, N | 1 |
| Reza Ashrafi, M | 1 |
| Heidari, M | 1 |
| Banwell, B | 1 |
| Garshasbi, M | 1 |
| Reza Tavasoli, A | 1 |
| Suezumi, K | 1 |
| Tagawa, A | 1 |
| Ogawa, T | 1 |
| Hashimoto, R | 1 |
| Otsuka, M | 1 |
| Kato, H | 1 |
| Yoshida, S | 1 |
| Kikuchi, A | 1 |
| Tateyama, M | 1 |
| Tano, O | 1 |
| Nishiyama, A | 1 |
| Akaishi, T | 1 |
| Kato, M | 1 |
| Aoki, M | 1 |
3 other studies available for prednisolone and Central Nervous System Demyelinating Diseases, Hereditary
| Article | Year |
|---|---|
Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy.
Topics: Amino Acid Substitution; Base Sequence; Brain; Child; Computer Simulation; Electron Transport; Elect | 2021 |
[Anti-NMDA receptor antibody-positive meningoencephalitis with SIADH and CNS demyelination: A case report].
Topics: Adult; Autoantibodies; Brain; Female; Hereditary Central Nervous System Demyelinating Diseases; Huma | 2018 |
A case of steroid-responsive MADSAM with late appearance of a partial conduction block in the forearm.
Topics: Anti-Inflammatory Agents; Forearm; Hereditary Central Nervous System Demyelinating Diseases; Humans; | 2014 |