methionine has been researched along with 7-Dehydrocholesterol Reductase Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Caglayan, AO; Ceylaner, G; Ceylaner, S; Degerliyurt, A; Hatipoglu, N; Hinderhofer, K; Kalb, S; Kurtoglu, S; Rehder, H; Schmid, S; Witsch-Baumgartner, M; Zschocke, J | 1 |
| Correa-Cerro, LS; Fliesler, SJ; Grinberg, A; Kratz, L; Miller, GF; Munasinghe, JP; Porter, FD; Wassif, CA | 1 |
2 other study(ies) available for methionine and 7-Dehydrocholesterol Reductase Deficiency
| Article | Year |
|---|---|
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey.
Topics: Adolescent; Child; Child, Preschool; Female; Humans; Male; Methionine; Mutation; Oxidoreductases Acting on CH-CH Group Donors; Smith-Lemli-Opitz Syndrome; Threonine; Turkey | 2012 |
Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy.
Topics: 3T3 Cells; Alleles; Amino Acid Substitution; Animals; Cells, Cultured; Crosses, Genetic; Disease Models, Animal; Embryonic Stem Cells; Female; Magnetic Resonance Spectroscopy; Methionine; Mice; Mice, Inbred C57BL; Mutagenesis, Site-Directed; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Simvastatin; Smith-Lemli-Opitz Syndrome; Threonine | 2006 |