dimethylamine has been researched along with Phenylketonurias in 1 studies
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
Excerpt | Relevance | Reference |
---|---|---|
"In contrast and unexpectedly, phenylketonuria patients had significantly lower ADMA plasma concentrations compared to controls (512±136 vs." | 5.38 | Asymmetric dimethylarginine in children with homocystinuria or phenylketonuria. ( Beckmann, B; Chobanyan-Jürgens, K; Das, AM; Illsinger, S; Kanzelmeyer, N; Lücke, T; Tsikas, D; Vaske, B, 2012) |
"In contrast and unexpectedly, phenylketonuria patients had significantly lower ADMA plasma concentrations compared to controls (512±136 vs." | 1.38 | Asymmetric dimethylarginine in children with homocystinuria or phenylketonuria. ( Beckmann, B; Chobanyan-Jürgens, K; Das, AM; Illsinger, S; Kanzelmeyer, N; Lücke, T; Tsikas, D; Vaske, B, 2012) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kanzelmeyer, N | 1 |
Tsikas, D | 1 |
Chobanyan-Jürgens, K | 1 |
Beckmann, B | 1 |
Vaske, B | 1 |
Illsinger, S | 1 |
Das, AM | 1 |
Lücke, T | 1 |
1 other study available for dimethylamine and Phenylketonurias
Article | Year |
---|---|
Asymmetric dimethylarginine in children with homocystinuria or phenylketonuria.
Topics: Adolescent; Amidohydrolases; Arginine; Cardiovascular Diseases; Child; Child, Preschool; Dimethylami | 2012 |