methylprednisolone has been researched along with Central Nervous System Demyelinating Diseases, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Banwell, B; Garshasbi, M; Heidari, E; Heidari, M; Pak, N; Rasoulinezhad, M; Reza Ashrafi, M; Reza Tavasoli, A | 1 |
| Hashimoto, R; Kato, H; Ogawa, T; Otsuka, M; Suezumi, K; Tagawa, A | 1 |
| Benetton, G; Di Vito, N; Fassio, F; Isoardo, G; Nobile, M | 1 |
3 other study(ies) available for methylprednisolone 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; Electron Transport Complex III; Female; Glucocorticoids; Hereditary Central Nervous System Demyelinating Diseases; Humans; Methylprednisolone; Models, Molecular; Mutation, Missense; Optic Atrophy, Hereditary, Leber; Prednisolone; Protein Conformation | 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; Humans; Inappropriate ADH Syndrome; Magnetic Resonance Imaging; Meningoencephalitis; Methylprednisolone; Neuroimaging; Prednisolone; Pulse Therapy, Drug; Receptors, N-Methyl-D-Aspartate | 2018 |
X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease.
Topics: Adult; Brain; Brain Stem; Cerebellum; Charcot-Marie-Tooth Disease; Connexins; Diagnosis, Differential; Disease Progression; DNA Mutational Analysis; Gap Junction beta-1 Protein; Genetic Diseases, X-Linked; Genetic Predisposition to Disease; Genetic Testing; Hereditary Central Nervous System Demyelinating Diseases; Humans; Magnetic Resonance Imaging; Male; Methylprednisolone; Multiple Sclerosis; Mutation; Oligoclonal Bands; Recurrence; Treatment Failure | 2005 |