leucine and Luft Disease

leucine has been researched along with Luft Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Emma, F; Salviati, L1
Bordoni, A; Bresolin, N; Ciscato, P; Comi, GP; Corti, S; Fassone, E; Govoni, A; Moggio, M; Ronchi, D; Sciacco, M; Virgilio, R1
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I1
Cain, BD; Hartzog, PE1

Reviews

1 review(s) available for leucine and Luft Disease

ArticleYear
Mitochondrial cytopathies and the kidney.
    Nephrologie & therapeutique, 2017, Volume: 13 Suppl 1

    Topics: DNA, Mitochondrial; Fanconi Syndrome; Humans; Kearns-Sayre Syndrome; Kidney Diseases; Leucine; Mitochondria; Mitochondrial Myopathies; Mutation; Oxidative Phosphorylation

2017

Other Studies

3 other study(ies) available for leucine and Luft Disease

ArticleYear
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment.
    Journal of the neurological sciences, 2010, May-15, Volume: 292, Issue:1-2

    Topics: Aged; Electron Transport Complex IV; Female; Humans; Leucine; Mitochondria; Mitochondrial Myopathies; Muscle, Skeletal; Mutation; Polymerase Chain Reaction; RNA, Transfer

2010
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.
    European journal of pediatrics, 1993, Volume: 152, Issue:8

    Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; Electron Transport Complex IV; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Male; Meglutol; Metabolism, Inborn Errors; Mitochondrial Myopathies; Respiration Disorders

1993
The aleu207-->arg mutation in F1F0-ATP synthase from Escherichia coli. A model for human mitochondrial disease.
    The Journal of biological chemistry, 1993, Jun-15, Volume: 268, Issue:17

    Topics: Amino Acid Sequence; Animals; Arginine; Escherichia coli; Genes, Bacterial; Humans; Kinetics; Leucine; Macromolecular Substances; Mitochondrial Myopathies; Models, Genetic; Molecular Sequence Data; Mutation; Oxidative Phosphorylation; Plasmids; Proton-Translocating ATPases; Sequence Homology, Amino Acid

1993