threonine has been researched along with Brain Diseases, Metabolic, Familial in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Allegri, AE; Briem, E; Buzzi, D; Caruso, U; Di Rocco, M; Rossi, A; Tiranti, V | 1 |
| De Vivo, DC; Fujii, T; Ho, YY; Ito, M; Kudo, T; Miyajima, T; Shirasaka, Y; Tsang, PT; Wang, D; Wong, HY | 1 |
| Ben-Neriah, Z; Darmin, PS; Dweikat, I; Gutman, A; Jakobs, C; Korman, SH; Salomons, GS; van der Knaap, MS; Wexler, ID | 1 |
3 other study(ies) available for threonine and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation.
Topics: Arginine; Biomarkers; Brain Diseases, Metabolic, Inborn; Child, Preschool; Diagnosis, Differential; Humans; Magnetic Resonance Imaging; Male; Malonates; Mitochondrial Proteins; Mutation; Nucleocytoplasmic Transport Proteins; Threonine | 2006 |
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 |
Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel.
Topics: Adolescent; Adult; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Isoleucine; Israel; Magnetic Resonance Imaging; Male; Mutation; Threonine | 2007 |