methionine has been researched along with Adult-Onset Dystonias in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
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, L | 1 |
Djuric, G; Dobricic, V; Jankovic, M; Kostic, VS; Kresojevic, N; Novakovic, I; Pekmezovic, T; Petrovic, I; Stefanova, E; Svetel, MV; Tomic, A | 1 |
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I | 1 |
Gollamudi, S; Jeon, BS; Kim, JY; Lee, JY; Ozelius, LJ | 1 |
1 review(s) available for methionine and Adult-Onset Dystonias
Article | Year |
---|---|
BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis.
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 |
3 other study(ies) available for methionine and Adult-Onset Dystonias
Article | Year |
---|---|
A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia.
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.
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.
Topics: Adult; Dystonic Disorders; Humans; Korea; Male; Methionine; Mutation; Parkinsonian Disorders; Sodium-Potassium-Exchanging ATPase; Threonine | 2007 |