lysine and Dystonia
lysine has been researched along with Dystonia in 8 studies
Research
Studies (8)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (12.50) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Atashpaz, S; Barbagiovanni, G; Boesch, S; Broccoli, V; Caiazzo, M; D'Antonio-Chronowska, A; Germain, PL; Haslinger, B; Jech, R; Lo Riso, P; Stewart, AF; Tenderini, E; Testa, G; Winkelmann, J; Zech, M | 1 |
| Arkadir, D; Barnicoat, A; Barral, S; Ben-Pazi, H; Bergman, H; Bhate, S; Bhatia, KP; Boys, A; Carr, LJ; Carss, KJ; Chong, WK; Chubb, JR; Dale, RC; Darin, N; Foulds, N; Gahl, WA; Gissen, P; Grozeva, D; Gutowski, N; Heales, SJ; Hills, A; Houlden, H; Hurst, JA; Israel, Z; Joseph, AP; Kaminska, M; Kamsteeg, EJ; Kurian, MA; Limousin, P; Lin, JP; Lumsden, D; McKee, S; Mencacci, NE; Meyer, E; Misra, S; Mohammed, SS; Morrogh, D; Nakou, V; Ng, J; Ngoh, A; Nichols, JM; Nicolai, J; Nilsson, M; Pall, H; Papandreou, A; Peall, KJ; Perez-Dueñas, B; Peters, GB; Pittman, A; Pope, S; Prabhakar, P; Rankin, J; Raymond, FL; Reis, A; Reuter, MS; Rump, P; Segel, R; Sinnema, M; Smith, M; Topf, M; Toro, C; Turnpenny, P; White, SM; Wieczorek, D; Wiethoff, S; Willemsen, MA; Wilson, BT; Winter, G; Wood, NW; Wragg, C | 1 |
| Kumar, KR; Siow, SF | 1 |
| Morton, DH; Puffenberger, EG; Robinson, DL; Strauss, KA | 1 |
| Camargos, ST; Cardoso, F; Gianetti, JG; Hardy, J; Lees, A; Momeni, P; Singleton, A | 1 |
| Dalton, RN; Howard, RS; Olpin, SE; Prevett, MC | 1 |
| Hirano, M; Imaiso, Y; Kaneda, N; Kira, J; Taniwaki, T; Ueno, S; Yamada, T; Yoshimura, T | 1 |
| Hill, R; Ryan, ED; Spate, M; Whelan, DT | 1 |
Other Studies
8 other study(ies) available for lysine and Dystonia
| Article | Year |
|---|---|
KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes.
Topics: Animals; Cell Differentiation; Cell Transdifferentiation; Dystonia; Embryo, Mammalian; Epigenesis, Genetic; Fibroblasts; Genetic Association Studies; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Methylation; Mice, Knockout; Myeloid-Lymphoid Leukemia Protein; Neurons; Transcriptome | 2018 |
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.
Topics: Adolescent; DNA-Binding Proteins; Dystonia; Female; Histone Methyltransferases; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Male; Methylation; Mutation; Nuclear Proteins | 2017 |
New gene implicated in early-onset generalized dystonia: Lysine-specific methyltransferase 2B (KMT2B).
Topics: Dystonia; Dystonic Disorders; Histone-Lysine N-Methyltransferase; Humans; Lysine; Methyltransferases | 2017 |
Type I glutaric aciduria, part 1: natural history of 77 patients.
Topics: Brain Diseases, Metabolic, Inborn; Chromosomes, Human, Pair 19; Dystonia; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Magnetic Resonance Imaging; Mutation; Necrosis; Oxidoreductases Acting on CH-CH Group Donors; Putamen; Tryptophan | 2003 |
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
Topics: Arginine; Brazil; Dopamine Agents; Dystonia; Family Health; GTP Cyclohydrolase; Humans; Levodopa; Lysine; Methionine; Mutation; Valine | 2008 |
Glutaric aciduria type 1 in adulthood.
Topics: Amino Acid Metabolism, Inborn Errors; Dystonia; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Middle Aged; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Tryptophan | 1996 |
A novel mutation of the GTP-cyclohydrolase I gene in a patient with hereditary progressive dystonia/dopa-responsive dystonia.
Topics: Adult; Circadian Rhythm; Dystonia; Electromyography; Female; GTP Cyclohydrolase; Humans; Levodopa; Lysine; Muscle, Skeletal; Point Mutation; Polymerase Chain Reaction; Threonine; Torticollis; Tremor | 1998 |
L-Glutaric acidemia: investigation of a patient and his family.
Topics: Amino Acid Metabolism, Inborn Errors; Consanguinity; Dystonia; Glutarates; Humans; Infant; Intellectual Disability; Lysine; Male; Oxidoreductases; Pedigree | 1979 |