proline has been researched along with Epilepsy, Absence in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bahlo, M; Cain, SM; David, LS; Foote, SJ; Garcia, E; Kyi, M; Ng, C; O'Brien, TJ; Powell, KL; Reid, CA; Sirdesai, S; Snutch, TP; Tyson, JR | 1 |
Emery, FA; Goldie, L; Stern, J | 1 |
2 other study(ies) available for proline and Epilepsy, Absence
Article | Year |
---|---|
A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
Topics: Animals; Animals, Newborn; Arginine; Biophysics; Calcium Channels, T-Type; Cell Line, Transformed; Disease Models, Animal; Electric Stimulation; Electroencephalography; Epilepsy, Absence; Exons; Humans; In Vitro Techniques; Membrane Potentials; Models, Molecular; Mutagenesis, Site-Directed; Patch-Clamp Techniques; Point Mutation; Proline; Protein Isoforms; Protein Structure, Tertiary; Rats; Rats, Transgenic; Seizures; Transfection | 2009 |
Hyperprolinaemia type 2.
Topics: Adolescent; Chromatography, Paper; Electroencephalography; Epilepsy, Absence; Female; Glycine; Humans; Hydroxyproline; Intellectual Disability; Metabolism, Inborn Errors; Proline | 1968 |