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phosphatidylcholines and Amino Acid Metabolism Disorders, Inborn

phosphatidylcholines has been researched along with Amino Acid Metabolism Disorders, Inborn in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hyötyläinen, T; Kurko, J; Lietzen, N; Mattila, I; Mykkänen, J; Näntö-Salonen, K; Niinikoski, H; Nygren, H; Olkku, A; Orešič, M; Pöhö, P; Simell, O; Tanner, L; Tringham, M; Vähä-Mäkilä, M1
Bottiglieri, T; Charles, HC; Gray, L; Hyland, K; Jaeken, J; Kahler, SG; Lazeyras, F; Van Hove, JL; Zeisel, SH1
Barranger, JA1
Boerescu, J; Tănase Mogoş, I1
Diekmann, E; Laryea, MD; Wendel, U1

Reviews

1 review(s) available for phosphatidylcholines and Amino Acid Metabolism Disorders, Inborn

ArticleYear
The implications of multiple forms of phenylalanine hydroxylase in phenylketonuria and related diseases of phenylalanine metabolism.
    Biochemical medicine, 1976, Volume: 15, Issue:1

    Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Female; Fetus; Genetic Variation; Gestational Age; Humans; Isoenzymes; Kinetics; Liver; Phenylalanine Hydroxylase; Phenylketonurias; Phosphatidylcholines; Pregnancy; Rats

1976

Other Studies

4 other study(ies) available for phosphatidylcholines and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Imbalance of plasma amino acids, metabolites and lipids in patients with lysinuric protein intolerance (LPI).
    Metabolism: clinical and experimental, 2016, Volume: 65, Issue:9

    Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Essential; Carbohydrate Metabolism; Child; Disease Progression; Energy Metabolism; Female; Finland; Glomerular Filtration Rate; Humans; Lipid Metabolism; Lipids; Lysine; Male; Middle Aged; Nitrites; Phosphatidylcholines; Triglycerides; Young Adult

2016
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels.
    Journal of inherited metabolic disease, 1998, Volume: 21, Issue:8

    Topics: Amino Acid Metabolism, Inborn Errors; Benzoic Acid; Brain Diseases; Choline; Coma; Female; Glycine; Homocysteine; Humans; Infant; Infant, Newborn; Male; Methionine; Methylation; Phosphatidylcholines; S-Adenosylmethionine; Seizures; Serine; Tetrahydrofolates

1998
[New types of congenital metabolic errors detected in newborn infants].
    Physiologie (Bucarest), 1975, Volume: 12, Issue:4

    Topics: Amines; Amino Acid Metabolism, Inborn Errors; Ascorbic Acid; Carbohydrate Metabolism, Inborn Errors; Female; Glucose; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lipid Metabolism, Inborn Errors; Male; Metabolism, Inborn Errors; Peptides; Phosphatidylcholines; Ribose

1975
Odd-numbered long-chain fatty acid contents in erythrocyte membrane phospholipids in patients with an impaired propionate utilization.
    Journal of inherited metabolic disease, 1988, Volume: 11 Suppl 2

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Erythrocyte Membrane; Fatty Acids; Humans; Infant; Infant, Newborn; Malonates; Methylmalonic Acid; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Propionates

1988