cysteine has been researched along with Epilepsies, Myoclonic 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 | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, C; Claes, LR; De Jonghe, P; Dondeti, RS; Gray, CB; Isom, LL; Lopez-Santiago, LF; Miyazaki, H; Nukina, N; O'Malley, HA; Oyama, F; Patino, GA; Slat, EA | 1 |
| Gökben, S; Klepper, J; Serdaroğlu, G; Tekgül, H; Yılmaz, S | 1 |
| Hong, SB; Joo, EY; Tae, WS | 1 |
3 other study(ies) available for cysteine and Epilepsies, Myoclonic
| Article | Year |
|---|---|
A functional null mutation of SCN1B in a patient with Dravet syndrome.
Topics: Animals; Arginine; Biophysics; Cell Line, Transformed; Cysteine; Disease Models, Animal; DNA Mutational Analysis; Electric Stimulation; Epilepsies, Myoclonic; Female; Green Fluorescent Proteins; Hippocampus; Humans; In Vitro Techniques; Infant; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Models, Molecular; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Oocytes; Polymorphism, Single Nucleotide; Sodium Channels; Temperature; Transfection; Twins; Voltage-Gated Sodium Channel beta-1 Subunit; Xenopus laevis | 2009 |
Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene.
Topics: Arginine; Child; Cysteine; Epilepsies, Myoclonic; Female; Glucose Transporter Type 1; Humans; Mutation | 2011 |
Cerebral blood flow abnormality in patients with idiopathic generalized epilepsy.
Topics: Adolescent; Adult; Brain; Brain Mapping; Cerebral Arteries; Cerebrovascular Circulation; Cerebrovascular Disorders; Cysteine; Down-Regulation; Epilepsies, Myoclonic; Epilepsy, Generalized; Epilepsy, Tonic-Clonic; Female; Humans; Male; Organotechnetium Compounds; Tomography, Emission-Computed, Single-Photon | 2008 |