citrulline and Encephalomyopathies, Mitochondrial

citrulline has been researched along with Encephalomyopathies, Mitochondrial in 1 studies

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
Birk, OS; Ferreira, CR; Manor, E; Staretz-Chacham, O; Wormser, O1

Other Studies

1 other study(ies) available for citrulline and Encephalomyopathies, Mitochondrial

ArticleYear
TMEM70 deficiency: Novel mutation and hypercitrullinemia during metabolic decompensation.
    American journal of medical genetics. Part A, 2019, Volume: 179, Issue:7

    Topics: Child, Preschool; Citrulline; Electron Transport; Female; Frameshift Mutation; Humans; Hyperammonemia; Infant, Newborn; Male; Membrane Proteins; Mitochondrial Encephalomyopathies; Mitochondrial Proteins; Pedigree

2019