arginine has been researched along with Developmental Psychomotor Disorders in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Auta, J; Davis, JM; Gatta, E; Guidotti, A; Pandey, SC; Zhang, H | 1 |
Bhatti, R; Kaur, A; Kaur, S; Singh, G | 1 |
DEHEVESY, G; HAMBRAEUS, L | 1 |
Harms, E; Homberger, A; Koch, HG; Linnebank, M; Marquardt, T; Rapp, B; Winter, C | 1 |
Christmann, D; Collard, M; Colombo, JP; Hirsch, E; Marescaux, C; Mutschler, V | 1 |
1 review(s) available for arginine and Developmental Psychomotor Disorders
Article | Year |
---|---|
[Late diagnosis of congenital argininemia during administration of sodium valproate].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Epilepsy; Female; Humans; Psychomotor Disorders; Valproic Acid | 1990 |
4 other study(ies) available for arginine and Developmental Psychomotor Disorders
Article | Year |
---|---|
Essential role for neuronal nitric oxide synthase in acute ethanol-induced motor impairment.
Topics: Alcohol-Induced Disorders, Nervous System; Animals; Arginine; Cerebellar Ataxia; Cerebellum; Enzyme Inhibitors; Ethanol; Frontal Lobe; Indazoles; Male; Nitric Oxide Synthase Type I; Psychomotor Disorders; Rats, Sprague-Dawley | 2020 |
Mercurius solubilis attenuates scopolamine-induced memory deficits and enhances the motor coordination in mice.
Topics: Analysis of Variance; Animals; Arginine; Avoidance Learning; Biphenyl Compounds; Calcimycin; Cholinergic Antagonists; Dose-Response Relationship, Drug; Enzyme Inhibitors; Female; Guanidines; Male; Maze Learning; Memory Disorders; Mercury; Mice; Neuroprotective Agents; Picrates; Psychomotor Disorders; Scopolamine | 2018 |
CYSTINURIA IN SWEDEN. VIII. A CASE OF COELIAC DISEASE ASSOCIATED WITH CYSTINE-LYSINURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Ataxia; Celiac Disease; Chromatography; Creatine; Creatinine; Cystinuria; Electrophoresis; Glucose Tolerance Test; Humans; Infant; Intestine, Small; Intestines; Lysine; Muscle Spasticity; Ornithine; Proteins; Psychomotor Disorders; Renal Aminoacidurias; Sweden; Urine; Vitamin A; Xylose | 1964 |
Two novel mutations (E86A, R113W) in argininosuccinate lyase deficiency and evidence for highly variable splicing of the human argininosuccinate lyase gene.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Argininosuccinate Lyase; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Hepatomegaly; Humans; Hyperammonemia; Point Mutation; Psychomotor Disorders; RNA Splicing; Sodium Benzoate | 2000 |