threonine has been researched along with Carbohydrate Metabolism, Inborn Error in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| De Vivo, DC; Fujii, T; Ho, YY; Ito, M; Kudo, T; Miyajima, T; Shirasaka, Y; Tsang, PT; Wang, D; Wong, HY | 1 |
| Hirabayashi, Y; Iida, N; Ishizuka, I; Kanzaki, T; Matsubara, T; Matsumoto, M; Matsumoto, Y; Toida, T; Yokota, M | 1 |
| Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
| Spiro, RG | 1 |
1 review(s) available for threonine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
Glycoproteins.
Topics: Amino Acids; Animals; Asparagine; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Chemical Phenomena; Chemistry; Enzymes; Glycoproteins; Hydroxyproline; Kinetics; Lysine; Polysaccharides; Serine; Threonine; Transferases | 1970 |
3 other study(ies) available for threonine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
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 |
Isolation and characterization of major urinary amino acid O-glycosides and a dipeptide O-glycoside from a new lysosomal storage disorder (Kanzaki disease). Excessive excretion of serine- and threonine-linked glycan in the patient urine.
Topics: Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Chromatography, Thin Layer; Glycopeptides; Glycosides; Humans; Magnetic Resonance Spectroscopy; Mass Spectrometry; Molecular Sequence Data; Serine; Threonine | 1990 |
Urinary amino acids in storage disorders: mucopolysaccharidosis, Gaucher's disease and metachromatic leucodystrophy.
Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; Female; Gaucher Disease; Glycolipids; Glycoproteins; Glycosaminoglycans; Humans; Intellectual Disability; Lysosomes; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Serine; Threonine; Tryptophan | 1969 |