tyrosine and Dystonia

tyrosine has been researched along with Dystonia in 11 studies

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19901 (9.09)18.7374
1990's2 (18.18)18.2507
2000's6 (54.55)29.6817
2010's2 (18.18)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
Asmus, F; Doherty, E; Gasser, T; King, MD; Langseth, A; Lynch, T; Munz, M; Nestor, T1
Fujioka, H; Kudo, S; Shintaku, H; Yamano, T1
Blau, N; Hoffmann, GF; Kühn, AA; Opladen, T1
Bandmann, O; Deuschl, G; Goertz, M; Hefter, H; Hoffmann, G; Jost, W; Müller, U; Oertel, W; Zöfel, P; Zschocke, J1
Champy, P; Duyckaerts, C; Féger, J; Hirsch, EC; Höglinger, GU; Khondiker, ME; Lannuzel, A; Lombes, A; Medja, F; Michel, PP; Oertel, WH; Prigent, A; Ruberg, M1
Anstey, NM; Boutlis, CS; Granger, DL; Hobbs, MR; Levesque, MC; Lopansri, BK; Maniboey, H; Mwaikambo, ED; Stoddard, GJ; Tjitra, E; Weinberg, JB1
Amaral, VG; Carducci, C; Giovanniello, T; Lorenzoni, PJ; Scola, RH; Teive, HA; Werneck, LC1
Arnold, LA; Bebin, EM; Fryburg, JS; Gunasekera, RS; Hyland, K; Jacobson, RD; Rost-Ruffner, E; Trugman, JM; Wilson, WG1
Arnold, LA; Hyland, K; Nygaard, TG; Sparagana, SP; Swoboda, KJ; Trugman, JM1
de Jong, AP; Haan, EA; Manson, JI; Ouvrier, RA; Wadman, SK; Wise, GA1

Trials

1 trial(s) available for tyrosine and Dystonia

ArticleYear
The phenylalanine loading test in the differential diagnosis of dystonia.
    Neurology, 2003, Feb-25, Volume: 60, Issue:4

    Topics: Administration, Oral; Adult; Diagnosis, Differential; Dystonia; Female; Humans; Levodopa; Male; Middle Aged; Phenylalanine; Predictive Value of Tests; Reference Values; Sensitivity and Specificity; Time Factors; Tyrosine

2003

Other Studies

10 other study(ies) available for tyrosine 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
"Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Apr-15, Volume: 24, Issue:5

    Topics: Adolescent; Adult; Age of Onset; Anticonvulsants; Antiparkinson Agents; Child; Child, Preschool; DNA Mutational Analysis; Dystonia; Exons; Female; Genetic Testing; Genotype; Humans; Hyperkinesis; Levodopa; Longitudinal Studies; Male; Middle Aged; Muscle, Skeletal; Mutation; Myoclonus; Nuclear Proteins; Phenotype; Sarcoglycans; Severity of Illness Index; Thyroid Nuclear Factor 1; Transcription Factors; Tyrosine; Young Adult

2009
Plasma phenylalanine level in dopa-responsive dystonia.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Nov-15, Volume: 24, Issue:15

    Topics: Analysis of Variance; Dihydroxyphenylalanine; Dopamine Agents; Dystonia; GTP Cyclohydrolase; Humans; Phenylalanine; Tyrosine

2009
Pitfalls in phenylalanine loading test in the diagnosis of dopa-responsive dystonia.
    Molecular genetics and metabolism, 2013, Volume: 108, Issue:3

    Topics: Administration, Oral; Adult; Biopterins; Diagnosis, Differential; Dystonia; Dystonic Disorders; Female; Humans; Levodopa; Metabolism, Inborn Errors; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Psychomotor Disorders; Tyrosine

2013
The mitochondrial complex I inhibitor rotenone triggers a cerebral tauopathy.
    Journal of neurochemistry, 2005, Volume: 95, Issue:4

    Topics: alpha-Synuclein; Amyloid beta-Peptides; Analysis of Variance; Animals; Antineoplastic Combined Chemotherapy Protocols; Behavior, Animal; Benzothiazoles; Body Weight; Caspase 3; Caspases; Cell Death; Cerebral Cortex; Cytarabine; Diagnostic Imaging; Dopamine and cAMP-Regulated Phosphoprotein 32; Doxorubicin; Dystonia; Electron Transport Complex III; Enzyme Activation; Glial Fibrillary Acidic Protein; Immunohistochemistry; Locomotion; Male; Microscopy, Electron, Transmission; Mitochondria; Neurons; Phosphopyruvate Hydratase; Phosphorylation; Posture; Psychomotor Performance; Rats; Rats, Inbred Lew; Rotenone; tau Proteins; Tauopathies; Thiazoles; Time Factors; Tyrosine; Tyrosine 3-Monooxygenase; Ubiquitin; Uncoupling Agents

2005
Elevated plasma phenylalanine in severe malaria and implications for pathophysiology of neurological complications.
    Infection and immunity, 2006, Volume: 74, Issue:6

    Topics: Child; Child, Preschool; Dystonia; Female; Humans; Infant; Malaria; Malaria, Cerebral; Male; Phenylalanine; Phenylalanine Hydroxylase; Tyrosine

2006
A novel missense mutation pattern of the GCH1 gene in dopa-responsive dystonia.
    Arquivos de neuro-psiquiatria, 2007, Volume: 65, Issue:4B

    Topics: Child; Dopamine Agents; Dystonia; Female; GTP Cyclohydrolase; Heterozygote; Humans; Levodopa; Mutation, Missense; Phenylalanine; Tyrosine

2007
Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test.
    Neurology, 1997, Volume: 48, Issue:5

    Topics: Administration, Oral; Adolescent; Adult; Aged; Aged, 80 and over; Aging; Biopterins; Child, Preschool; Dihydroxyphenylalanine; Dopamine Agents; Dystonia; Female; Humans; Male; Middle Aged; Neopterin; Osmolar Concentration; Phenylalanine; Time Factors; Tyrosine

1997
Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency.
    Journal of inherited metabolic disease, 1999, Volume: 22, Issue:3

    Topics: Administration, Oral; Dopamine; Dystonia; Genetic Diseases, Inborn; GTP Cyclohydrolase; Heterozygote; Humans; Phenylalanine; Tyrosine

1999
Kinetic study of catecholamine metabolism in hereditary progressive dystonia.
    Neuropediatrics, 1989, Volume: 20, Issue:1

    Topics: Adolescent; Catecholamines; Child; Dystonia; Female; Humans; Levodopa; Tyrosine

1989