arginine has been researched along with Developmental Disabilities in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (16.67) | 18.7374 |
| 1990's | 1 (8.33) | 18.2507 |
| 2000's | 3 (25.00) | 29.6817 |
| 2010's | 5 (41.67) | 24.3611 |
| 2020's | 1 (8.33) | 2.80 |
| Authors | Studies |
|---|---|
| Arunachalam, P; Choe, CU; Gelderblom, M; Gerloff, C; Jensen, M; Magnus, T; Müller, C; Schwedhelm, E; Zeller, T | 1 |
| Birnbaum, R; Gur, H; Kidron, D; Lerman-Sagie, T; Lev, D; Malinger, G; Yanoov-Sharav, M; Yosha-Orpaz, N; Yosovich, K | 1 |
| Galvanovskis, J; Hasegawa, S; Horita, S; Kumamoto, K; Maejima, Y; Shimomura, K; Takenoshita, S | 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 |
| Briand, G; Cheillan, D; Feillet, F; Montaut-Verient, B; Schmitt, E; Sorlin, A; Wiedemann, A | 1 |
| Fuchs, O; Pfarr, N; Pohlenz, J; Schmidt, H | 1 |
| Amin, HJ; Sauve, RS; Soraisham, AS | 1 |
| Aubin, I; Barnhart, KF; Benavides, F; Brandon, JL; Conti, CJ; DiGiovanni, J; Gimenez-Conti, I; Giulivi, C; Guénet, JL; Jaubert, J; Kusewitt, DF; Otto, NW; Perez, CJ; Quintanilla, VC; Ross-Inta, CM | 1 |
| Izkovitch, S; Korman, SH; Levy, N; Mandel, H | 1 |
| Gök, F; Gökçay, E; Gül, D; Sayli, BS | 1 |
| Hambraeus, L; Hardell, LI; Hjorth, G; Lorentsson, R; Westphal, O | 1 |
| Maagoe, H | 1 |
2 trial(s) available for arginine and Developmental Disabilities
| 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 |
Neurodevelopmental outcomes of premature infants treated with l-arginine for prevention of necrotising enterocolitis.
Topics: Alberta; Arginine; Blindness; Cerebral Palsy; Child, Preschool; Cognition Disorders; Deafness; Developmental Disabilities; Enterocolitis, Necrotizing; Female; Follow-Up Studies; Humans; Infant, Newborn; Male; Premature Birth; Treatment Outcome | 2009 |
10 other study(ies) available for arginine and Developmental Disabilities
| Article | Year |
|---|---|
Homoarginine- and Creatine-Dependent Gene Regulation in Murine Brains with l-Arginine:Glycine Amidinotransferase Deficiency.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Arginine; Brain; Creatine; Developmental Disabilities; Gene Expression Regulation; Glycine; Homoarginine; Intellectual Disability; Mice; Mice, Inbred C57BL; Speech Disorders; Stroke | 2020 |
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.
Topics: Arginine; Astrocytoma; Brachydactyly; Developmental Disabilities; Female; Fetal Growth Retardation; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Methylation; Muscle Hypotonia; Mutation; Orbital Neoplasms; Pregnancy; Protein-Arginine N-Methyltransferases | 2019 |
Water intake disorder in a DEND syndrome afflicted patient with R50P mutation.
Topics: Amino Acid Substitution; Animals; Arginine; Child; Developmental Disabilities; Drinking; Epilepsy; Humans; Hyperglycemia; Male; Models, Molecular; Mutation, Missense; Potassium Channels, Inwardly Rectifying; Proline; Rats; Rats, Wistar; Syndrome | 2015 |
Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency.
Topics: Alanine Transaminase; Arginine; Aspartate Aminotransferases; Child; Child, Preschool; Deafness; Developmental Disabilities; Fatty Acids; Female; Humans; Infant; Membrane Proteins; Muscle Hypotonia; Peroxisomal Disorders; Phytanic Acid; Pipecolic Acids; Sialorrhea | 2016 |
Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation.
Topics: Arginine; Child; Chorea; Developmental Disabilities; DNA Mutational Analysis; Enzyme-Linked Immunosorbent Assay; Histidine; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Monocarboxylic Acid Transporters; Mutation; Symporters; Triiodothyronine | 2009 |
Two hypomorphic alleles of mouse Ass1 as a new animal model of citrullinemia type I and other hyperammonemic syndromes.
Topics: Alleles; Animals; Arginine; Argininosuccinate Synthase; Blotting, Western; Cell Movement; Cerebellum; Citrullinemia; Developmental Disabilities; Disease Models, Animal; Female; Growth Disorders; Humans; Hyperammonemia; Immunoenzyme Techniques; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Mutant Strains; Mutation, Missense; Nitric Oxide; Phenotype; Sodium Benzoate; Syndrome | 2010 |
Elevated plasma citrulline and arginine due to consumption of Citrullus vulgaris (watermelon).
Topics: Adult; Arginine; Citrulline; Citrullinemia; Citrullus; Developmental Disabilities; Diet; Female; Humans; Infant; Models, Biological; Nutritional Requirements; Urea | 2005 |
IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-).
Topics: Arginine; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 18; Developmental Disabilities; Dwarfism, Pituitary; Growth Hormone; Humans; IgA Deficiency; Insulin; Intellectual Disability; Levodopa; Male; Pituitary Function Tests; Propranolol; Sequence Deletion | 1994 |
Argininosuccinic aciduria. Report of three cases and the effect of high and reduced protein intake on the clinical state.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Blood Urea Nitrogen; Cerebellar Ataxia; Child; Developmental Disabilities; Diet Therapy; Dietary Proteins; Electroencephalography; Female; Hair; Humans; Intellectual Disability; Succinates | 1974 |
Argininosuccinic aciduria. A case.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Child, Preschool; Developmental Disabilities; Diet Therapy; Humans; Infant; Infant, Newborn; Male; Succinates | 1969 |