valine has been researched along with Chorea in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (12.50) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (50.00) | 29.6817 |
2010's | 1 (12.50) | 24.3611 |
2020's | 2 (25.00) | 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 |
Heim, B; Seppi, K | 1 |
Bashir, H; Jankovic, J | 1 |
Bird, TD; Chen, DH; Feleke, A; Fink, J; Lipe, H; Matsushita, M; Meaney, B; Rainier, S; Raskind, WH; Tisch, L; Wolff, J | 1 |
Djarmati, A; Dragasević, N; Klein, C; Kostić, VS; Momcilović, D; Stefanova, E; Svetel, M | 1 |
Asmus, F; Chinnery, PF; Devlin, A; Gasser, T; Munz, M; Zimprich, A | 1 |
Fialkow, RZ; Haria, DM; Maru, MC | 1 |
Bruck, J; Gerstenbrand, F; Gnad, H; Gründig, E; Prosenz, P; Simanyi, M | 1 |
1 review(s) available for valine and Chorea
Article | Year |
---|---|
Treatment options for chorea.
Topics: Antipsychotic Agents; Chorea; Deep Brain Stimulation; Dopamine Antagonists; Humans; Piperidines; Tetrabenazine; Transcranial Magnetic Stimulation; Valine; Vesicular Monoamine Transport Proteins | 2018 |
7 other study(ies) available for valine and Chorea
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 |
Valbenazine as treatment for Huntington's disease chorea.
Topics: Chorea; Humans; Huntington Disease; Tetrabenazine; Valine | 2023 |
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
Topics: Alanine; Amino Acid Substitution; Chorea; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutational Analysis; Exons; Female; Genes, Dominant; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Haplotypes; Humans; Male; Muscle Proteins; Mutation, Missense; Pedigree; Protein Structure, Secondary; Valine | 2005 |
Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.
Topics: Adolescent; Adult; Alanine; Chorea; DNA Mutational Analysis; Family Health; Female; Humans; Male; Middle Aged; Muscle Proteins; Mutation; Valine; Yugoslavia | 2006 |
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 |
Choreiform movements in dialysis patient taking valacyclovir and famciclovir.
Topics: 2-Aminopurine; Acyclovir; Aged; Aged, 80 and over; Chorea; Drug Interactions; Famciclovir; Herpes Zoster; Humans; Kidney Failure, Chronic; Male; Renal Dialysis; Valacyclovir; Valine | 2001 |
[The effect of the administration of amino acids, especially of L-dopa and alpha-methyldopa, on the composition of cerebrospinal fluid in extrapyramidal syndromes. II. Alterations of cerebrospinal fluid in patients with Parkinson's disease and chorea fol
Topics: Alanine Transaminase; Amino Acids; Aspartate Aminotransferases; Chorea; Humans; Methyldopa; Parkinson Disease; Valine | 1969 |