threonine and Glycine Encephalopathy

threonine has been researched along with Glycine Encephalopathy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Friederich, MW; Gabel, L; Ghaloul-Gonzalez, L; Miller, K; Neira-Fresneda, J; Peck, C; Schlichting, L; Swanson, MA; Tong, S; Van Hove, JLK; Young, SP1
Ben-Neriah, Z; Boneh, A; Kanno, J; Korman, SH; Kure, S; Lerer, I; Matsubara, Y; Sato, K1

Other Studies

2 other study(ies) available for threonine and Glycine Encephalopathy

ArticleYear
Cerebrospinal fluid amino acids glycine, serine, and threonine in nonketotic hyperglycinemia.
    Journal of inherited metabolic disease, 2022, Volume: 45, Issue:4

    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.
    Journal of human genetics, 2005, Volume: 50, Issue:5

    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