valine has been researched along with CACH Syndrome 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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ahmed, R; Fox, NC; Guerreiro, R; Guven, G; Hardy, J; Rohrer, JD; Rossor, MN | 1 |
| Arighi, A; Bassi, MT; Bresolin, N; De Riz, M; Fumagalli, GG; Galimberti, D; Ghezzi, L; Jacini, F; Pietroboni, AM; Rango, M; Scarpini, E; Tenderini, E | 1 |
2 other study(ies) available for valine and CACH Syndrome
| Article | Year |
|---|---|
A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids.
Topics: Aged; Alanine; Family Health; Female; Fluorodeoxyglucose F18; Genetic Testing; Humans; Leukoencephalopathies; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Positron-Emission Tomography; Receptor, Macrophage Colony-Stimulating Factor; Valine | 2013 |
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation.
Topics: Aged; Alanine; Eukaryotic Initiation Factor-2B; Female; Humans; Leukoencephalopathies; Mutation; Valine | 2012 |