methylprednisolone has been researched along with Genetic Diseases, X-Chromosome Linked in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheung, PW; Cooper, CM; Linnoila, JJ; Penney, EB | 1 |
| Arata, Y; Hinamoto, N; Inoue-Torii, A; Kakio, Y; Kato, A; Kitagawa, M; Ogawa-Akiyama, A; Sugiyama, H; Uchida, HA; Wada, J | 1 |
| Hashimura, Y; Hayakawa, A; Iijima, K; Kanegane, H; Matsuo, M; Miyawaki, T; Nakanishi, K; Nozu, K; Takemoto, M; Yoshikawa, N | 1 |
| Benetton, G; Di Vito, N; Fassio, F; Isoardo, G; Nobile, M | 1 |
4 other study(ies) available for methylprednisolone and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Case 15-2020: A 79-Year-Old Man with Hyponatremia and Involuntary Movements of the Arm and Face.
Topics: Aged; Arm; Blood Chemical Analysis; Diagnosis, Differential; Dyskinesias; Encephalitis; Face; Genetic Diseases, X-Linked; Glucocorticoids; Hashimoto Disease; Humans; Hyponatremia; Inappropriate ADH Syndrome; Intracellular Signaling Peptides and Proteins; Male; Methylprednisolone; Osmolar Concentration; Sodium | 2020 |
IgA Nephropathy Complicated with X-linked Thrombocytopenia.
Topics: Adolescent; Genetic Diseases, X-Linked; Glomerulonephritis, IGA; Humans; Male; Methylprednisolone; Thrombocytopenia; Tonsillectomy | 2018 |
Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Topics: CD4-Positive T-Lymphocytes; Child, Preschool; Cyclosporine; DNA; Forkhead Transcription Factors; Gene Deletion; Genetic Diseases, X-Linked; Humans; Immunosuppressive Agents; Interleukin-2 Receptor alpha Subunit; Male; Methylprednisolone; Nephrotic Syndrome; Polyendocrinopathies, Autoimmune; Protein-Losing Enteropathies; Secondary Prevention; Sequence Analysis, DNA; T-Lymphocytes, Regulatory; Treatment Outcome | 2009 |
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 |