mevalonic acid has been researched along with Recrudescence in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aktas, O; Brocke, S; Dorr, J; Endres, M; Nitsch, R; Prozorovski, T; Sallach, S; Seeger, B; Smorodchenko, A; Waiczies, S; Zipp, F | 1 |
Jones, PJ | 1 |
De Jong, JG; Drenth, JP; Kremer, HP; Scheffer, H; Simon, A; Van Der Meer, JW; Wevers, RA | 1 |
de Barse, MM; de Koning, TJ; Dorland, L; Duran, M; Frenkel, J; Houten, SM; Huijbers, WA; Kuis, W; Poll-The, BT; Rijkers, GT; Romeijn, GJ; van Royen-Kerkhof, A; Wanders, RJ; Waterham, HR | 1 |
1 review(s) available for mevalonic acid and Recrudescence
Article | Year |
---|---|
Statin rebound effect?
Topics: Humans; Hydroxymethylglutaryl CoA Reductases; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hyperlipoproteinemia Type II; Mevalonic Acid; Recurrence; Up-Regulation | 2003 |
3 other study(ies) available for mevalonic acid and Recrudescence
Article | Year |
---|---|
Treatment of relapsing paralysis in experimental encephalomyelitis by targeting Th1 cells through atorvastatin.
Topics: Animals; Apoptosis; Atorvastatin; CD4-Positive T-Lymphocytes; Cell Cycle; Cell Division; Cell Line; Encephalomyelitis, Autoimmune, Experimental; Female; Genes, MHC Class II; Heptanoic Acids; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Mevalonic Acid; Mice; Mice, Inbred Strains; Myelin Proteolipid Protein; Paralysis; Peptide Fragments; Pyrroles; Recurrence; Spinal Cord; Th1 Cells | 2003 |
Mevalonate kinase deficiency: Evidence for a phenotypic continuum.
Topics: Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Enzyme Activation; Exanthema; Female; Fever; Humans; Immunoglobulin D; Infant; Lymphatic Diseases; Male; Mevalonic Acid; Middle Aged; Mutation; Periodicity; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Recurrence; Registries; Syndrome | 2004 |
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome.
Topics: Amino Acid Substitution; Cloning, Molecular; Escherichia coli; Female; Fever; Genes, Recessive; Humans; Hypergammaglobulinemia; Immunoglobulin D; Indonesia; Lymphocytes; Male; Mevalonic Acid; Netherlands; Periodicity; Phosphotransferases (Alcohol Group Acceptor); Point Mutation; Recombinant Proteins; Recurrence; Syndrome | 1999 |