arginine and allysine

arginine has been researched along with allysine in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Hoffmann, GF; Koeller, DM; Kölker, S; Okun, JG; Opp, S; Sauer, SW1
Al Teneiji, A; Bruun, TU; Cordeiro, D; Inbar-Feigenberg, M; Mercimek-Mahmutoglu, S; Patel, J; Struys, E; Weiss, S1
Bouchereau, J; Schiff, M1

Reviews

1 review(s) available for arginine and allysine

ArticleYear
Inherited Disorders of Lysine Metabolism: A Review.
    The Journal of nutrition, 2020, 10-01, Volume: 150, Issue:Suppl 1

    Topics: 2-Aminoadipic Acid; Aldehyde Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Arginine; Brain; Brain Diseases, Metabolic; Brain Diseases, Metabolic, Inborn; Carnitine; Epilepsy; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Metabolic Diseases; Pyridoxal Phosphate; Pyridoxine

2020

Other Studies

2 other study(ies) available for arginine and allysine

ArticleYear
Therapeutic modulation of cerebral L-lysine metabolism in a mouse model for glutaric aciduria type I.
    Brain : a journal of neurology, 2011, Volume: 134, Issue:Pt 1

    Topics: 2-Aminoadipate Transaminase; 2-Aminoadipic Acid; Amino Acid Metabolism, Inborn Errors; Analysis of Variance; Animals; Arginine; Brain; Brain Diseases, Metabolic; Carnitine; Catalase; Glutaryl-CoA Dehydrogenase; Ketoglutaric Acids; Lysine; Mice

2011
Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy.
    Metabolic brain disease, 2017, Volume: 32, Issue:2

    Topics: 2-Aminoadipic Acid; Adolescent; Aldehyde Dehydrogenase; Arginine; Child; Child, Preschool; Cohort Studies; Epilepsy; Female; Genotype; Humans; Infant; Lysine; Male; Mutation, Missense; Phenotype; Pyridoxine; Retrospective Studies; Seizures; Treatment Outcome; Vitamins

2017
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