cysteine and Luft Disease

cysteine has been researched along with Luft Disease in 3 studies

Research

Studies (3)

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

Authors

AuthorsStudies
Galetta, F; Logerfo, A; Mancuso, M; Murri, L; Nesti, C; Orsucci, D; Petrozzi, L; Rocchi, A; Santoro, G; Siciliano, G1
Azan, G; Bonilla, E; DiMauro, S; Ferraris, S; Hirano, M; Krishna, S; Mancuso, M; Mauro, A; Nishigaki, Y; Romansky, SG; Sammarco, P; Tay, SK1
Anders, MW1

Reviews

1 review(s) available for cysteine and Luft Disease

ArticleYear
Mitochondrial bioactivation of cysteine S-conjugates and 4-thiaalkanoates: implications for mitochondrial dysfunction and mitochondrial diseases.
    Biochimica et biophysica acta, 1995, May-24, Volume: 1271, Issue:1

    Topics: Animals; Biotransformation; Cysteine; Glutathione Transferase; Humans; Hydrocarbons, Halogenated; Microsomes; Mitochondria; Mitochondrial Myopathies; Organelles; Oxidative Phosphorylation

1995

Trials

1 trial(s) available for cysteine and Luft Disease

ArticleYear
Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation.
    Journal of neurology, 2010, Volume: 257, Issue:5

    Topics: Antioxidants; Biomarkers; Cross-Over Studies; Cysteine; Double-Blind Method; Female; Humans; Lactic Acid; Male; Middle Aged; Mitochondrial Myopathies; Oxidative Stress; Quality of Life; Severity of Illness Index; Treatment Outcome

2010

Other Studies

1 other study(ies) available for cysteine and Luft Disease

ArticleYear
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
    Journal of the neurological sciences, 2005, Jan-15, Volume: 228, Issue:1

    Topics: Cysteine; Cytochrome-c Oxidase Deficiency; Diabetes Complications; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Electron Transport Complex II; Electron Transport Complex III; Female; Humans; Infant; Male; Middle Aged; Mitochondrial Myopathies; Muscle, Skeletal; Point Mutation; RNA, Transfer; Threonine

2005