valine has been researched along with Adult-Onset Dystonias in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cances, C; Damaj, L; de Lonlay, P; Doummar, D; Espil, C; Fluss, J; François-Heude, MC; Kern, I; Lebigot, E; Leboucq, N; Lenaers, G; Meyer, P; Munnich, A; Roubertie, A; Roze, E; Spitz, MA; Torre, S; Touati, G; Warde, MTA | 1 |
| Cheng, FB; Feng, JC; Grundmann, K; Ma, LY; Miao, J; Ott, T; Wan, XH | 1 |
| 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 |
| Asmus, F; Chinnery, PF; Devlin, A; Gasser, T; Munz, M; Zimprich, A | 1 |
1 review(s) available for valine 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 |
4 other study(ies) available for valine and Adult-Onset Dystonias
| Article | Year |
|---|---|
Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies.
Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Chorea; Coenzyme A; Dystonia; Dystonic Disorders; Enoyl-CoA Hydratase; Humans; Leigh Disease; Movement Disorders; Thiolester Hydrolases; Valine | 2022 |
Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.
Topics: Adult; Apoptosis Regulatory Proteins; Asian People; Aspartic Acid; Cell Line, Tumor; Cohort Studies; DNA Mutational Analysis; DNA-Binding Proteins; Dystonic Disorders; Female; Genetic Predisposition to Disease; Genotype; HEK293 Cells; Humans; Male; Molecular Chaperones; Mutation; Neuroblastoma; Nuclear Proteins; Transfection; Valine | 2014 |
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 |
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
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 |