Compounds > arginine

arginine and Dystonia

arginine has been researched along with Dystonia in 6 studies

Research

Studies (6)

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

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

Other Studies

6 other study(ies) available for arginine and Dystonia

Article	Year
A novel phenotype in an Italian family with a rare progranulin mutation. Journal of neurology, 2022, Volume: 269, Issue:11 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. Movement disorders : official journal of the Movement Disorder Society, 2009, Dec-15, Volume: 24, Issue:16 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. Parkinsonism & related disorders, 2012, Volume: 18, Issue:5 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. Movement disorders : official journal of the Movement Disorder Society, 2004, Volume: 19, Issue:5 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. Neuroscience letters, 2006, May-01, Volume: 398, Issue:1-2 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. Movement disorders : official journal of the Movement Disorder Society, 2008, Jan-30, Volume: 23, Issue:2 Topics: Arginine; Brazil; Dopamine Agents; Dystonia; Family Health; GTP Cyclohydrolase; Humans; Levodopa; Lysine; Methionine; Mutation; Valine	2008