arginine has been researched along with Auditory Processing Disorder, Central in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 8 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fu, Q; Gao, H; Jiang, M; Lin, W; Lin, Y; Lu, B; Zheng, T; Zhou, S; Zhu, L | 1 |
| 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 |
| Mhanni, AA; Prasad, C; Rockman-Greenberg, C | 1 |
| Boenzi, S; Boiani, A; Dionisi-Vici, C; Goffredo, BM; Martinelli, D; Pastore, A; Rizzo, C | 1 |
2 review(s) available for arginine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review.
Topics: Arginine; Argininosuccinate Synthase; Asian People; Base Sequence; China; Citrulline; Citrullinemia; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Infant, Newborn; Language Development Disorders; Male; Mutation; Pedigree; Phenotype; Phenylalanine; RNA Splicing | 2019 |
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 Auditory Processing Disorder, Central
| 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 |
5 other study(ies) available for arginine and Auditory Processing Disorder, Central
| 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 |
Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood.
Topics: Abdominal Pain; Alkalosis, Respiratory; Arginine; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child, Preschool; Citrulline; Consciousness Disorders; Diagnosis, Differential; Diet, Protein-Restricted; Emergencies; Exons; Female; Glutamine; Humans; Hyperammonemia; Language Development Disorders; Liver Transplantation; Mutation, Missense; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Recurrence | 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 |