Compounds > citrulline

citrulline and Abnormalities, Multiple

citrulline has been researched along with Abnormalities, Multiple in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bardet, J; Diry, C; Heron, B; Kamoun, P; Marsac, C; Munnich, A; Parvy, P; Ponsot, G; Rabier, D; Rotig, A; Rustin, P; Saudubray, JM1
Gallagher, AC; Pike, M; Standing, S1

Other Studies

2 other study(ies) available for citrulline and Abnormalities, Multiple

ArticleYear
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
    Journal of inherited metabolic disease, 1998, Volume: 21, Issue:3

    Topics: Abnormalities, Multiple; Ataxia; Biomarkers; Child, Preschool; Citrulline; DNA, Mitochondrial; Female; Glycine; Humans; Infant; Male; Muscular Diseases; Mutation; Retinitis Pigmentosa; Threonine

1998
HHH syndrome associated with callosal agenesis and disordered neuronal migration.
    Developmental medicine and child neurology, 2001, Volume: 43, Issue:6

    Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Bronchopulmonary Sequestration; Citrulline; Consanguinity; Female; Humans; Hyperammonemia; Infant; Metabolism, Inborn Errors; Ornithine; Phenotype; Syndrome

2001