Page last updated: 2024-09-04

phenyldiazene and Glycine Encephalopathy

phenyldiazene has been researched along with Glycine Encephalopathy in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Applegarth, DA; Coulter-Mackie, MB; James, ER; Toone, JR	1

Other Studies

1 other study(ies) available for phenyldiazene and Glycine Encephalopathy

Article	Year
Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH). Molecular genetics and metabolism, 2001, Volume: 72, Issue:4 Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; DNA Primers; Exons; Gene Frequency; Glycine; Glycine Dehydrogenase (Decarboxylating); Heterozygote; Humans; Hydroxymethyl and Formyl Transferases; Hyperglycinemia, Nonketotic; Imines; Infant, Newborn; Ketosis; Liver; Mutation; Polymerase Chain Reaction; Prenatal Diagnosis	2001

Article

Year

Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).

Molecular genetics and metabolism, 2001, Volume: 72, Issue:4

Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; DNA Primers; Exons; Gene Frequency; Glycine; Glycine Dehydrogenase (Decarboxylating); Heterozygote; Humans; Hydroxymethyl and Formyl Transferases; Hyperglycinemia, Nonketotic; Imines; Infant, Newborn; Ketosis; Liver; Mutation; Polymerase Chain Reaction; Prenatal Diagnosis

2001