tryptophan has been researched along with Brain Diseases, Metabolic, Familial in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Morton, DH; Puffenberger, EG; Robinson, DL; Strauss, KA | 1 |
Cornelio, AR; de Souza Wyse, AT; Dutra-Filho, CS; Rodrigues, V; Wajner, M; Wannmacher, CM | 1 |
Cornelio, A; Dutra-Filho, CS; Feksa, LR; Wajner, M; Wannmacher, CM; Wyse, AT | 1 |
De Vivo, DC; Fujii, T; Ho, YY; Ito, M; Kudo, T; Miyajima, T; Shirasaka, Y; Tsang, PT; Wang, D; Wong, HY | 1 |
Cheng, KC; Connor, JR; Goodman, SI; Housman, C; Jacobs, RE; LaNoue, K; Lazovic, J; O'Callaghan, JP; Simpson, I; Woontner, M; Zinnanti, WJ | 1 |
5 other study(ies) available for tryptophan and Brain Diseases, Metabolic, Familial
Article | Year |
---|---|
Type I glutaric aciduria, part 1: natural history of 77 patients.
Topics: Brain Diseases, Metabolic, Inborn; Chromosomes, Human, Pair 19; Dystonia; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Magnetic Resonance Imaging; Mutation; Necrosis; Oxidoreductases Acting on CH-CH Group Donors; Putamen; Tryptophan | 2003 |
Tryptophan reduces creatine kinase activity in the brain cortex of rats.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Cerebral Cortex; Creatine Kinase; Disease Models, Animal; Down-Regulation; Energy Metabolism; Glutathione; Oxidative Stress; Rats; Rats, Wistar; Tryptophan | 2004 |
The effects of the interactions between amino acids on pyruvate kinase activity from the brain cortex of young rats.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Binding Sites; Brain Diseases, Metabolic, Inborn; Cerebral Cortex; Cystine; Energy Metabolism; Feedback, Physiological; Nerve Degeneration; Phenylalanine; Pyruvate Kinase; Rats; Rats, Wistar; Serine; Tryptophan | 2005 |
Three Japanese patients with glucose transporter type 1 deficiency syndrome.
Topics: 3-Hydroxybutyric Acid; Adult; Arginine; Brain Diseases, Metabolic, Inborn; Brain Mapping; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glucose Transporter Type 1; Humans; Japan; Male; Methionine; Mutation, Missense; Positron-Emission Tomography; Threonine; Tryptophan | 2007 |
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I.
Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Homoarginine; Humans; Lysine; Mice; Mice, Knockout; Mitochondria; Neurons; Nuclear Magnetic Resonance, Biomolecular; Tryptophan | 2007 |