Compounds > arginine

arginine and Adult-Onset Dystonias

arginine has been researched along with Adult-Onset Dystonias in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, JZ; Demircioglu, FE; Ingram, J; Ploegh, HL; Schwartz, TU; Sosa, BA1
Bhatia, KP; Cordivari, C; Koukouni, V; Quinn, NP; Valente, EM1
Asmus, F; Chinnery, PF; Devlin, A; Gasser, T; Munz, M; Zimprich, A1
Bonifati, V; Chang, HC; Chen, RS; Lu, CS; Weng, YH; Wu-Chou, YH1

Other Studies

4 other study(ies) available for arginine and Adult-Onset Dystonias

ArticleYear
How lamina-associated polypeptide 1 (LAP1) activates Torsin.
    eLife, 2014, Aug-22, Volume: 3

    Topics: Adenosine Triphosphatases; Amino Acid Sequence; Arginine; Binding Sites; Crystallography, X-Ray; Cytoskeletal Proteins; Dystonic Disorders; Humans; Membrane Proteins; Microscopy, Electron; Models, Molecular; Molecular Chaperones; Molecular Sequence Data; Mutation; Nuclear Envelope; Nuclear Proteins; Protein Binding; Protein Multimerization; Protein Structure, Tertiary; Sequence Homology, Amino Acid

2014
Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp.
    Movement disorders : official journal of the Movement Disorder Society, 2008, Oct-15, Volume: 23, Issue:13

    Topics: Adolescent; Adult; Arginine; DNA Mutational Analysis; Dystonic Disorders; Family Health; Female; Humans; Male; Mutation; Myoclonus; Sarcoglycans; Young Adult

2008
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
    Movement disorders : official journal of the Movement Disorder Society, 2007, Oct-31, Volume: 22, Issue:14

    Topics: Adolescent; Arginine; Child; Chorea; DNA Mutational Analysis; Dystonic Disorders; Exons; Family Health; Female; Genotype; Glycine; Humans; Male; Mutation; Myoclonus; Nuclear Proteins; Sarcoglycans; Thyroid Nuclear Factor 1; Transcription Factors; Valine

2007
Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.
    Parkinsonism & related disorders, 2008, Volume: 14, Issue:5

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Arginine; Child; DNA Mutational Analysis; Dystonic Disorders; Female; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Multiple System Atrophy; Mutation; Protein Serine-Threonine Kinases; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Taiwan

2008