threonine has been researched along with Glycine Encephalopathy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Friederich, MW; Gabel, L; Ghaloul-Gonzalez, L; Miller, K; Neira-Fresneda, J; Peck, C; Schlichting, L; Swanson, MA; Tong, S; Van Hove, JLK; Young, SP | 1 |
| Ben-Neriah, Z; Boneh, A; Kanno, J; Korman, SH; Kure, S; Lerer, I; Matsubara, Y; Sato, K | 1 |
2 other study(ies) available for threonine and Glycine Encephalopathy
| Article | Year |
|---|---|
Cerebrospinal fluid amino acids glycine, serine, and threonine in nonketotic hyperglycinemia.
Topics: Amino Acids; Cross-Sectional Studies; Glycine; Humans; Hyperglycinemia, Nonketotic; Infant, Newborn; Serine; Threonine | 2022 |
A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem.
Topics: Amino Acid Oxidoreductases; Amino Acid Substitution; Arabs; Codon, Initiator; Female; Glycine; Glycine Dehydrogenase (Decarboxylating); Humans; Hyperglycinemia, Nonketotic; Israel; Male; Methionine; Pedigree; Point Mutation; RNA, Messenger; Threonine | 2005 |