Compounds > tryptophan

tryptophan and Dystonia

tryptophan has been researched along with Dystonia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anikster, Y; Ben-Zeev, B; Benoist, JF; Berutti, R; Blau, N; Bruggmann, R; Cremer, K; Dorboz, I; Engels, H; Gahl, WA; Gemperle-Britschgi, C; Guarani, V; Haack, TB; Harper, JW; Heimer, G; Hoffmann, GF; Huttlin, EL; Imbard, A; Keller, I; Landau, Y; Malicdan, MCV; Marek-Yagel, D; Martinez, A; Mayatepek, E; Meili, D; Meissner, T; Meitinger, T; Mullikin, JC; Opladen, T; Paulo, JA; Pode-Shakked, B; Prokisch, H; Schiff, M; Schwartz, G; Shen, N; Strom, TM; Thöny, B; Trefz, FK; Vilboux, T; Ziv-Strasser, L1
Morton, DH; Puffenberger, EG; Robinson, DL; Strauss, KA1
Dalton, RN; Howard, RS; Olpin, SE; Prevett, MC1
Curran, SP; Koehler, CM; Roesch, K; Tranebjaerg, L1

Other Studies

4 other study(ies) available for tryptophan and Dystonia

ArticleYear
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability.
    American journal of human genetics, 2017, 02-02, Volume: 100, Issue:2

    Topics: Alleles; Amino Acid Sequence; Biopterins; Case-Control Studies; Dopamine; Dystonia; Exons; Female; Fibroblasts; Gene Deletion; Genome-Wide Association Study; HSP70 Heat-Shock Proteins; Humans; Intellectual Disability; Male; Pedigree; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Repressor Proteins; Serotonin; Tryptophan; Tryptophan Hydroxylase; Tyrosine; Tyrosine 3-Monooxygenase

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
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
Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex.
    Human molecular genetics, 2002, Mar-01, Volume: 11, Issue:5

    Topics: Amino Acid Substitution; Carrier Proteins; Cells, Cultured; Deafness; DNA-Binding Proteins; Dystonia; Fibroblasts; Humans; Intracellular Membranes; Membrane Transport Proteins; Mitochondria; Mitochondrial Precursor Protein Import Complex Proteins; Molecular Weight; Mutation, Missense; Point Mutation; Syndrome; Tryptophan

2002