arginine has been researched along with Dystonia in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Barone, P; Cicarelli, G; Cuoco, S; Gagliardi, M; Pellecchia, MT; Procopio, R; Quattrone, A; Russillo, MC; Scarpa, A; Sorrentino, C; Talarico, M; Vinciguerra, C | 1 |
Gorostidi, A; Indakoetxea, B; Martí Massó, JF; Mok, KY; Paisán-Ruiz, C; Ruibal, M; Ruiz-Martinez, J | 1 |
Groffen, AJ; Hilgevoord, AA; Linssen, WH; Tijssen, MA; van Rootselaar, AF; van Strien, TW | 1 |
Arai, H; Fujihara, K; Ichinose, H; Itoyama, Y; Kikuchi, A; Kimpara, T; Nagai, M; Okamura, N; Shiga, Y; Takeda, A; Tanji, H; Urano, F | 1 |
Richter, A; Sander, SE | 1 |
Camargos, ST; Cardoso, F; Gianetti, JG; Hardy, J; Lees, A; Momeni, P; Singleton, A | 1 |
6 other study(ies) available for arginine and Dystonia
Article | Year |
---|---|
A novel phenotype in an Italian family with a rare progranulin mutation.
Topics: Arginine; Dysphonia; Dystonia; Frontotemporal Dementia; Histidine; Humans; Intercellular Signaling Peptides and Proteins; Mutation; Phenotype; Progranulins; Respiratory Sounds | 2022 |
Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Apoptosis Regulatory Proteins; Arginine; Child; DNA-Binding Proteins; Dystonia; Exons; Female; Humans; Male; Middle Aged; Mutation; Nuclear Proteins; Young Adult | 2009 |
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.
Topics: Adolescent; Arginine; Chromosomes, Human, Pair 16; Codon, Terminator; DNA Mutational Analysis; Dyskinesias; Dystonia; Electroencephalography; Epilepsy, Benign Neonatal; Family Health; Female; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Membrane Proteins; Mutation; Nerve Tissue Proteins; Seizures | 2012 |
Arg(184)His mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa-responsive dystonia with parkinsonism: a case report.
Topics: Antiparkinson Agents; Arginine; Brain; Dystonia; Genes, Recessive; GTP Cyclohydrolase; Humans; Levodopa; Magnetic Resonance Imaging; Male; Middle Aged; Parkinsonian Disorders; Pedigree; Phenylketonurias; Point Mutation; Tomography, Emission-Computed; Tomography, Emission-Computed, Single-Photon | 2004 |
Striatal microinjections of nitric oxide synthase inhibitors and L-arginine fail to exert effects on paroxysmal dystonia in the dtsz mutant.
Topics: Animals; Arginine; Corpus Striatum; Cricetinae; Dystonia; Indazoles; Microinjections; Motor Activity; Mutation; Nitric Oxide; Nitric Oxide Synthase Type I | 2006 |
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
Topics: Arginine; Brazil; Dopamine Agents; Dystonia; Family Health; GTP Cyclohydrolase; Humans; Levodopa; Lysine; Methionine; Mutation; Valine | 2008 |