Compounds > citrulline

citrulline and Electron Transport Chain Deficiencies, Mitochondrial

citrulline has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 6 studies

Research

Studies (6)

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

Authors

AuthorsStudies
Cowan, TM; Cusmano-Ozog, KP; Enns, GM; Hall, PL; Lee, CU; Mendelsohn, BA; Stander, Z; Tise, CG; Verscaj, CP; Woods, J1
Demczko, MM; Ganetzky, RD; He, M; Hong, X; Master, SR; Wongkittichote, P1
Falk, MJ; Ganetzky, RD1
Al-Hertani, W; Modabber, M; Toffoli, D; Wilson, N; Zakrzewski, H1
Atkuri, KR; Cowan, TM; Enns, GM; Herzenberg, LA; Kwan, T; Ng, A1
Abu-Libdeh, B; Gutman, A; Kanazawa, N; Korman, SH; Tsujino, S1

Other Studies

6 other study(ies) available for citrulline and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
MT-ATP6 mitochondrial disease identified by newborn screening reveals a distinct biochemical phenotype.
    American journal of medical genetics. Part A, 2023, Volume: 191, Issue:6

    Topics: Citrulline; Humans; Infant, Newborn; Mitochondrial Diseases; Mitochondrial Proton-Translocating ATPases; Neonatal Screening; Pedigree; Urea Cycle Disorders, Inborn

2023
Low Plasma Citrulline Guiding the Diagnosis of a Mitochondrial Disorder.
    Clinical chemistry, 2023, 06-01, Volume: 69, Issue:6

    Topics: Arginine; Citrulline; Humans; Mitochondrial Diseases

2023
8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease.
    Molecular genetics and metabolism, 2018, Volume: 123, Issue:3

    Topics: Adolescent; Adult; Arginine; Brain; Child; Child, Preschool; Citrulline; DNA, Mitochondrial; Female; Humans; Infant; Infusions, Intravenous; Magnetic Resonance Imaging; Male; Mitochondria; Mitochondrial Diseases; Nitric Oxide; Prospective Studies; Retrospective Studies; Stroke; Treatment Outcome; Young Adult

2018
Infantile Presentation of Leber Hereditary Optic Neuropathy "Plus" Disease.
    Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society, 2019, Volume: 39, Issue:2

    Topics: Administration, Oral; Child, Preschool; Citrulline; DNA, Mitochondrial; Humans; Magnetic Resonance Imaging; Male; Mitochondrial Diseases; Mutation; Optic Atrophy, Hereditary, Leber; Tomography, Optical Coherence; Ubiquinone; Visual Acuity

2019
Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia.
    Proceedings of the National Academy of Sciences of the United States of America, 2009, Mar-10, Volume: 106, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Blood Cells; Citrulline; Glutathione; Humans; Intracellular Space; Mitochondria; Mitochondrial Diseases; Protein Carbonylation; Reactive Oxygen Species

2009
Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family.
    Journal of the neurological sciences, 2004, Mar-15, Volume: 218, Issue:1-2

    Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; Arabs; Child, Preschool; Citrulline; DNA Mutational Analysis; Exons; Family Health; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Hyperammonemia; Lactic Acid; Male; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Ornithine; Polymerase Chain Reaction; Proteins

2004