valine has been researched along with Seizures, Febrile in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chudley, AE; Hartley, JN; Mhanni, AA; Sanger, WG; Spriggs, EL | 1 |
| Hoshi, A; Ogiwara, I; Sugiura, Y; Ugawa, Y; Yamakawa, K | 1 |
| Chou, IC; Lee, CC; Lin, SS; Tsai, CH; Tsai, FJ | 1 |
3 other study(ies) available for valine and Seizures, Febrile
| Article | Year |
|---|---|
Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder.
Topics: Child, Preschool; Epilepsy; Gene Expression Regulation; Genes, Dominant; Genetic Variation; Humans; Leucine; Male; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Pedigree; Seizures, Febrile; Sodium Channels; Valine | 2011 |
Different degrees of loss of function between GEFS+ and SMEI Nav 1.1 missense mutants at the same residue induced by rescuable folding defects.
Topics: Arginine; Aspartic Acid; Biophysics; Cell Line, Transformed; Electric Stimulation; Epilepsies, Myoclonic; Humans; Membrane Potentials; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Patch-Clamp Techniques; Seizures, Febrile; Sodium Channels; Transfection; Valine | 2012 |
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in febrile seizures.
Topics: Alleles; Asian People; Brain-Derived Neurotrophic Factor; Case-Control Studies; Child; Gene Frequency; Genetic Markers; Genotype; Heterozygote; Homozygote; Humans; Methionine; Polymorphism, Single Nucleotide; Seizures, Febrile; Taiwan; Valine | 2004 |