arginine has been researched along with Dyskinesia Syndromes in 16 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (31.25) | 18.7374 |
| 1990's | 2 (12.50) | 18.2507 |
| 2000's | 2 (12.50) | 29.6817 |
| 2010's | 7 (43.75) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Angle, B; Araújo, HC; Barshop, B; Coskun, T; Diogo, L; Geraghty, M; Grolik, C; Haliloglu, G; Konstantopoulou, V; Korenke, GC; Leuzzi, V; Levtova, A; Longo, N; Mackenzie, J; Maranda, B; Marquart, I; Mercimek-Mahmutoglu, S; Mhanni, AA; Mitchell, G; Morris, A; Newlove, T; Nyhan, W; Renaud, D; Scaglia, F; Schlune, A; Schulze, A; Stockler-Ipsiroglu, S; Valayannopoulos, V; van Karnebeek, C; van Spronsen, FJ; Verbruggen, KT; Yuskiv, N | 1 |
| Braissant, O | 1 |
| Nguyen, T; Pitt, JJ; Tzanakos, N | 1 |
| Atzler, D; Chobanyan-Jürgens, K; Choe, CU; Frölich, JC; Huneau, JF; Kayacelebi, AA; Langen, J; Lücke, T; Mariotti, F; Rothmann, S; Schneider, JY; Schwedhelm, E; Tsikas, D; Weigt-Usinger, K | 1 |
| Iqbal, F | 1 |
| Bishnoi, M; Chopra, K; Kulkarni, SK | 1 |
| Bebbington, A; Downs, J; Foley, KR; Girdler, S; Jacoby, P; Kaufmann, WE; Leonard, H | 1 |
| Boenzi, S; Boiani, A; Dionisi-Vici, C; Goffredo, BM; Martinelli, D; Pastore, A; Rizzo, C | 1 |
| Puukka, M; Ruokonen, A; Similä, S; von Wendt, L | 1 |
| Dietrich, WD; Kuluz, JW; Prado, RJ; Schleien, CL; Watson, BD | 1 |
| Abeles, I; Covault, J; Deckel, AW; Gary, KA; Sasso, D; Schmerler, N; Volmer, P; Watts, D; Weiner, R; Yan, Z | 1 |
| Bachmann, C; Bordugo, A; Burlina, AB; Colombo, JP; Ferrari, V; Wermuth, B; Zacchello, F | 1 |
| Baryshnikov, VA; Ermolina, LA; Turova, NF | 1 |
| Fluharty, AL; Kihara, H; Porter, MT; Valente, M | 1 |
| Bicknell, J; Cavanagh, NP; Howard, F | 1 |
| Hart, B; Hooper, PT; Smith, GW | 1 |
1 review(s) available for arginine and Dyskinesia Syndromes
| Article | Year |
|---|---|
Review: Human guanidinoacetate n-methyl transferase (GAMT) deficiency: A treatable inborn error of metabolism.
Topics: Arginine; Creatine; Dietary Proteins; Dietary Supplements; Energy Metabolism; Genetic Predisposition to Disease; Guanidinoacetate N-Methyltransferase; Humans; Language Development Disorders; Movement Disorders; Phenotype; Treatment Outcome | 2015 |
1 trial(s) available for arginine and Dyskinesia Syndromes
| Article | Year |
|---|---|
Biosynthesis of homoarginine (hArg) and asymmetric dimethylarginine (ADMA) from acutely and chronically administered free L-arginine in humans.
Topics: Adolescent; Adult; Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Arginine; Child; Coronary Artery Disease; Developmental Disabilities; Female; Guanidinoacetate N-Methyltransferase; Homoarginine; Humans; Intellectual Disability; Language Development Disorders; Male; Mice; Mice, Knockout; Middle Aged; Movement Disorders; Peripheral Arterial Disease; Speech Disorders | 2015 |
14 other study(ies) available for arginine and Dyskinesia Syndromes
| Article | Year |
|---|---|
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring.
Topics: Adolescent; Adult; Arginine; Brain; Child; Child, Preschool; Combined Modality Therapy; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Infant; Infant, Newborn; Intellectual Disability; Language Development Disorders; Male; Middle Aged; Movement Disorders; Ornithine; Practice Guidelines as Topic; Sodium Benzoate; Treatment Outcome; Young Adult | 2014 |
GAMT deficiency: 20 years of a treatable inborn error of metabolism.
Topics: Arginine; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disability; Language Development Disorders; Male; Movement Disorders; Ornithine; Sodium Benzoate | 2014 |
Newborn screening for guanidinoacetate methyl transferase deficiency.
Topics: Arginine; Creatine; Diet; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disability; Language Development Disorders; Male; Metabolism, Inborn Errors; Movement Disorders; Ornithine; Sodium Benzoate | 2014 |
Co-administration of nitric oxide (NO) donors prevents haloperidol-induced orofacial dyskinesia, oxidative damage and change in striatal dopamine levels.
Topics: Animals; Antipsychotic Agents; Arginine; Chromatography, High Pressure Liquid; Citrulline; Dopamine; Dyskinesia, Drug-Induced; Haloperidol; Male; Molsidomine; Movement Disorders; Neostriatum; Nitric Oxide Donors; Oxidative Stress; Rats; Rats, Wistar; Superoxides | 2009 |
Change in gross motor abilities of girls and women with rett syndrome over a 3- to 4-year period.
Topics: Adolescent; Adult; Age Factors; Arginine; Australia; Disease Progression; Female; Humans; Linear Models; Longitudinal Studies; Methyl-CpG-Binding Protein 2; Motor Skills; Movement Disorders; Mutation; Retrospective Studies; Rett Syndrome; Young Adult | 2011 |
Creatine metabolism in urea cycle defects.
Topics: Adolescent; Adult; Amidinotransferases; Arginine; Child; Child, Preschool; Creatine; Female; Guanidinoacetate N-Methyltransferase; Humans; Infant; Language Development Disorders; Male; Movement Disorders; Nerve Tissue Proteins; Ornithine-Oxo-Acid Transaminase; Plasma Membrane Neurotransmitter Transport Proteins; Urea Cycle Disorders, Inborn; Young Adult | 2012 |
Argininosuccinic aciduria in a Finnish woman presenting with psychosis and mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Argininosuccinic Acid; Female; Humans; Intellectual Disability; Middle Aged; Movement Disorders; Schizophrenia | 1982 |
The effect of nitric oxide synthase inhibition on infarct volume after reversible focal cerebral ischemia in conscious rats.
Topics: Amino Acid Oxidoreductases; Animals; Arginine; Body Weight; Cerebral Infarction; Ischemic Attack, Transient; Male; Movement Disorders; NG-Nitroarginine Methyl Ester; Nitric Oxide; Nitric Oxide Synthase; Rats; Rats, Wistar | 1993 |
Dietary arginine alters time of symptom onset in Huntington's disease transgenic mice.
Topics: Animals; Arginine; Blood Glucose; Brain; Cerebrovascular Circulation; Diet; Huntington Disease; Mice; Mice, Transgenic; Movement Disorders; Time Factors; Tyrosine; Weight Loss | 2000 |
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disorders.
Topics: Acetyltransferases; Amino-Acid N-Acetyltransferase; Ammonia; Arginine; Benzoates; Benzoic Acid; Brain; Dietary Proteins; Female; Humans; Infant; Magnetic Resonance Imaging; Movement Disorders; Orotic Acid | 1992 |
[Characteristics of the amino acid spectrum of the blood of children with intellectual deficiency].
Topics: Amino Acids; Ammonia; Arginine; Aspartic Acid; Child; Female; Glutamates; Glutamic Acid; Humans; Intellectual Disability; Male; Movement Disorders; Polyamines; Syndrome; Urea | 1986 |
Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Antipsychotic Agents; Arginine; Chlorpromazine; Cystinuria; Female; Fluphenazine; Humans; Intellectual Disability; Intestinal Absorption; Kidney Tubules; Lysine; Movement Disorders; Ornithine; Pedigree; Renal Aminoacidurias; Thioridazine; Trihexyphenidyl | 1973 |
Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers.
Topics: Arginine; Child; Cystinuria; Humans; Intellectual Disability; Lysine; Male; Movement Disorders; Ornithine | 1974 |
The prevention and treatment of Birdsville disease of horses.
Topics: Aminocaproates; Animals; Arachis; Arginine; Australia; Canavanine; Diet Therapy; Dietary Proteins; Food Additives; Gelatin; Hindlimb; Horse Diseases; Horses; Movement Disorders; Plant Poisoning | 1971 |