methylprednisolone has been researched along with Luft Disease in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Peterson, PL | 1 |
Fabrizi, GM; Guazzi, GC; Malandrini, A; Manneschi, L; Parrotta, E; Rosi, R; Scarpini, C | 1 |
Alder, H; Argov, Z; Bank, W; Chavin, JM; DiMauro, S; Heiman-Patterson, TD; Kalman, B; Tahmoush, AJ | 1 |
1 trial(s) available for methylprednisolone and Luft Disease
Article | Year |
---|---|
The treatment of mitochondrial myopathies and encephalomyopathies.
Topics: Adolescent; Adult; Age of Onset; Antioxidants; Ascorbic Acid; Child; Coenzymes; Female; Humans; Kearns-Sayre Syndrome; Male; MELAS Syndrome; MERRF Syndrome; Methylprednisolone; Middle Aged; Mitochondrial Myopathies; Oxidative Phosphorylation; Oxygen Consumption; Treatment Outcome; Ubiquinone; Vitamin E; Vitamin K; Vitamins | 1995 |
2 other study(ies) available for methylprednisolone and Luft Disease
Article | Year |
---|---|
Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: report of a case.
Topics: Aged; Arteritis; Dose-Response Relationship, Drug; Eye Diseases; Fatal Outcome; Female; Humans; Methylprednisolone; Mitochondria, Muscle; Mitochondrial Myopathies; Neurologic Examination; Respiratory Insufficiency | 1995 |
Biochemical and genetic studies in a family with mitochondrial myopathy.
Topics: Adolescent; Adult; Child; Child, Preschool; DNA, Mitochondrial; Female; Gene Rearrangement; Glucocorticoids; Humans; Male; Methylprednisolone; Microscopy, Electron; Middle Aged; Mitochondrial Myopathies; Muscles; Mutation; Pedigree; Polymorphism, Genetic | 1997 |