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dimethylamine and Phenylketonurias

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).

Research Excerpts

ExcerptRelevanceReference
"In contrast and unexpectedly, phenylketonuria patients had significantly lower ADMA plasma concentrations compared to controls (512±136 vs."5.38Asymmetric 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."1.38Asymmetric 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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kanzelmeyer, N1
Tsikas, D1
Chobanyan-Jürgens, K1
Beckmann, B1
Vaske, B1
Illsinger, S1
Das, AM1
Lücke, T1

Other Studies

1 other study available for dimethylamine and Phenylketonurias

ArticleYear
Asymmetric dimethylarginine in children with homocystinuria or phenylketonuria.
    Amino acids, 2012, Volume: 42, Issue:5

    Topics: Adolescent; Amidohydrolases; Arginine; Cardiovascular Diseases; Child; Child, Preschool; Dimethylami

2012