lysine has been researched along with Epilepsies, Myoclonic in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chang, CY; Chang, FC; Chen, CY; Chen, YT; Fan, HH; Hsiao, JH; Khorkova, O; Lee, LJ; Lee, ML; Lin, SW; Liou, HH; Tsai, MS; Yanagawa, Y; You, JY; Yu, IS | 1 |
| García-Villoria, J; Girós, M; Ribes, A; Ruiz, A; Torres, MA; Tort, F; Ugarteburu, O | 1 |
| Hanna, MG; Harding, AE; Morgan-Hughes, JA; Nelson, IP | 1 |
| Amati, P; Antozzi, C; Bresolin, N; DiDonato, S; Piccolo, G; Toscano, A; Zeviani, M | 1 |
4 other study(ies) available for lysine and Epilepsies, Myoclonic
| Article | Year |
|---|---|
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development.
Topics: Action Potentials; Age Factors; Animals; Animals, Newborn; Dentate Gyrus; Disease Models, Animal; Epilepsies, Myoclonic; gamma-Aminobutyric Acid; Glutamate Decarboxylase; Hyperthermia, Induced; In Vitro Techniques; Lysine; Male; Mice; Mice, Transgenic; Models, Molecular; Mutation; NAV1.1 Voltage-Gated Sodium Channel; Nerve Net; Neurons; Seizures | 2015 |
Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient.
Topics: Child; Diet; Epilepsies, Myoclonic; Female; Homozygote; Humans; Hyperlysinemias; Lactic Acid; Lysine; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Nervous System Malformations; Phosphotransferases (Alcohol Group Acceptor); Pipecolic Acids; Pyridoxal Phosphate; RNA, Messenger; Vitamin B Complex | 2016 |
Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA.
Topics: Autoradiography; Blotting, Northern; Cells, Cultured; DNA, Mitochondrial; Epilepsies, Myoclonic; Humans; Lysine; Male; Middle Aged; Mitochondria, Muscle; Muscles; Phenotype; Point Mutation; Protein Biosynthesis; RNA, Transfer, Lys | 1995 |
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).
Topics: Base Sequence; DNA, Mitochondrial; Epilepsies, Myoclonic; Humans; Lysine; Mitochondria, Muscle; Molecular Sequence Data; Muscles; Mutation; Pedigree; Polymerase Chain Reaction; RNA, Transfer, Lys; Syndrome | 1991 |