Compounds > threonine

threonine and Dystonia

threonine has been researched along with Dystonia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Date, H; Hashimoto, T; Ikeda, S; Naito, K; Okano, T; Onodera, O; Sekijima, Y; Tsuji, S1
Rodacker, V; Toustrup-Jensen, M; Vilsen, B1
Hirano, M; Imaiso, Y; Kaneda, N; Kira, J; Taniwaki, T; Ueno, S; Yamada, T; Yoshimura, T1

Other Studies

3 other study(ies) available for threonine and Dystonia

ArticleYear
Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation.
    Movement disorders : official journal of the Movement Disorder Society, 2003, Volume: 18, Issue:10

    Topics: Adolescent; Apraxias; Brain Mapping; Cerebellum; DNA Mutational Analysis; DNA-Binding Proteins; Dystonia; Female; Humans; Hypoalbuminemia; Magnetic Resonance Imaging; Mutation; Nuclear Proteins; Ocular Motility Disorders; Polymerase Chain Reaction; Threonine

2003
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
    The Journal of biological chemistry, 2006, Jul-07, Volume: 281, Issue:27

    Topics: Animals; Chlorocebus aethiops; COS Cells; Dystonia; Genetic Predisposition to Disease; Humans; Models, Molecular; Mutation; Parkinsonian Disorders; Phenylalanine; Protein Conformation; Rats; Sodium; Sodium-Potassium-Exchanging ATPase; Threonine

2006
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