Page last updated: 2024-08-17

methionine and Adult-Onset Dystonias

methionine 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's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alonso-Canovas, A; Bernal-Bernal, I; Blanco-Ollero, A; Bonilla-Toribio, M; Burguera, JA; Cáceres-Redondo, MT; Carballo, M; Carrillo, F; Catalán-Alonso, MJ; Escamilla-Sevilla, F; Espinosa-Rosso, R; Fernández-Moreno, MC; García-Caldentey, J; García-Moreno, JM; García-Ruiz, PJ; Giacometti-Silveira, S; Gómez-Garre, P; Gutiérrez-García, J; Huertas-Fernández, I; Jesús, S; López-Valdés, E; Martínez-Castrillo, JC; Martínez-Torres, I; Medialdea-Natera, MP; Méndez-Lucena, C; Mínguez-Castellanos, A; Mir, P; Moya, M; Ochoa-Sepulveda, JJ; Ojea, T; Rodríguez, N; Sillero-Sánchez, M; Vargas-González, L1
Djuric, G; Dobricic, V; Jankovic, M; Kostic, VS; Kresojevic, N; Novakovic, I; Pekmezovic, T; Petrovic, I; Stefanova, E; Svetel, MV; Tomic, A1
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I1
Gollamudi, S; Jeon, BS; Kim, JY; Lee, JY; Ozelius, LJ1

Reviews

1 review(s) available for methionine and Adult-Onset Dystonias

ArticleYear
BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis.
    Movement disorders : official journal of the Movement Disorder Society, 2014, Volume: 29, Issue:8

    Topics: Adult; Aged; Brain-Derived Neurotrophic Factor; Case-Control Studies; Dystonic Disorders; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Valine

2014

Other Studies

3 other study(ies) available for methionine and Adult-Onset Dystonias

ArticleYear
A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia.
    Acta neurologica Belgica, 2013, Volume: 113, Issue:3

    Topics: Adult; Age of Onset; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Dystonic Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Odds Ratio; Parkinson Disease; Polymorphism, Single Nucleotide; Valine

2013
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5

    Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia

2005
ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.
    Movement disorders : official journal of the Movement Disorder Society, 2007, Sep-15, Volume: 22, Issue:12

    Topics: Adult; Dystonic Disorders; Humans; Korea; Male; Methionine; Mutation; Parkinsonian Disorders; Sodium-Potassium-Exchanging ATPase; Threonine

2007