Compounds > methionine
Page last updated: 2024-08-17

methionine and Abnormal Movements

methionine has been researched along with Abnormal Movements in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
de Lau, LM; Heutink, P; Marinus, J; van Hilten, JJ; Verbaan, D1
Dean, DJ; Lunsford-Avery, J; Mittal, VA; Pelletier, AL; Smith, A; Smolen, A1
Harada, S; Hayashi, A; Nakamura, T; Ohkoshi, N; Shoji, S; Watanabe, M; Yoshizawa, K1
Cousens, SN; Estibeiro, K; Green, AJ; Ironside, JW; Knight, RS; Mackenzie, J; Macleod, MA; Stewart, GE; Will, RG; Zeidler, M1

Other Studies

4 other study(ies) available for methionine and Abnormal Movements

ArticleYear
Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease.
    Movement disorders : official journal of the Movement Disorder Society, 2012, Volume: 27, Issue:1

    Topics: Aged; Antiparasitic Agents; Catechol O-Methyltransferase; Cohort Studies; Dyskinesia, Drug-Induced; Dyskinesias; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Proportional Hazards Models; Valine

2012
BDNF Val66Met and spontaneous dyskinesias in non-clinical psychosis.
    Schizophrenia research, 2012, Volume: 140, Issue:1-3

    Topics: Adolescent; Adult; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Dyskinesias; Female; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult

2012
Association between catechol-O-methyltransferase gene polymorphisms and wearing-off and dyskinesia in Parkinson's disease.
    Neuropsychobiology, 2003, Volume: 48, Issue:4

    Topics: Aged; Catechol O-Methyltransferase; Dyskinesias; Exons; Fatigue Syndrome, Chronic; Female; Genotype; Humans; Male; Methionine; Parkinson Disease; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sequence Analysis, DNA; Valine

2003
Diagnosis of new variant Creutzfeldt-Jakob disease.
    Annals of neurology, 2000, Volume: 47, Issue:5

    Topics: Adolescent; Adult; Ataxia; Brain; Codon; Cognition Disorders; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Dyskinesias; Female; Homozygote; Humans; Magnetic Resonance Imaging; Male; Mental Disorders; Methionine; Middle Aged; Neuropsychological Tests; Population Surveillance; Prions; Sensitivity and Specificity; United Kingdom

2000