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lysine and Dystonia

lysine has been researched along with Dystonia in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's2 (25.00)18.2507
2000's2 (25.00)29.6817
2010's3 (37.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, M1
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, C1
Kumar, KR; Siow, SF1
Morton, DH; Puffenberger, EG; Robinson, DL; Strauss, KA1
Camargos, ST; Cardoso, F; Gianetti, JG; Hardy, J; Lees, A; Momeni, P; Singleton, A1
Dalton, RN; Howard, RS; Olpin, SE; Prevett, MC1
Hirano, M; Imaiso, Y; Kaneda, N; Kira, J; Taniwaki, T; Ueno, S; Yamada, T; Yoshimura, T1
Hill, R; Ryan, ED; Spate, M; Whelan, DT1

Other Studies

8 other study(ies) available for lysine and Dystonia

ArticleYear
KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes.
    Cell reports, 2018, 10-23, Volume: 25, Issue:4

    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.
    Nature genetics, 2017, Volume: 49, Issue:2

    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).
    Movement disorders : official journal of the Movement Disorder Society, 2017, Volume: 32, Issue:3

    Topics: Dystonia; Dystonic Disorders; Histone-Lysine N-Methyltransferase; Humans; Lysine; Methyltransferases

2017
Type I glutaric aciduria, part 1: natural history of 77 patients.
    American journal of medical genetics. Part C, Seminars in medical genetics, 2003, Aug-15, Volume: 121C, Issue:1

    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.
    Movement disorders : official journal of the Movement Disorder Society, 2008, Jan-30, Volume: 23, Issue:2

    Topics: Arginine; Brazil; Dopamine Agents; Dystonia; Family Health; GTP Cyclohydrolase; Humans; Levodopa; Lysine; Methionine; Mutation; Valine

2008
Glutaric aciduria type 1 in adulthood.
    Journal of neurology, neurosurgery, and psychiatry, 1996, Volume: 60, Issue:3

    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.
    Neurology, 1998, Volume: 50, Issue:2

    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.
    Pediatrics, 1979, Volume: 63, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Consanguinity; Dystonia; Glutarates; Humans; Infant; Intellectual Disability; Lysine; Male; Oxidoreductases; Pedigree

1979