Compounds > arginine

arginine and Luft Disease

arginine has been researched along with Luft Disease in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ding, X; Han, Y; Yang, Z; Yi, Y; Yu, H2
Hashiguchi, A; Higuchi, I; Higuchi, Y; Nozuma, S; Okamoto, Y; Sakiyama, Y; Takashima, H; Yoshimura, A; Yuan, J1
Boneh, A; Coman, D; Yaplito-Lee, J1
Cain, BD; Hartzog, PE1

Reviews

1 review(s) available for arginine and Luft Disease

ArticleYear
New indications and controversies in arginine therapy.
    Clinical nutrition (Edinburgh, Scotland), 2008, Volume: 27, Issue:4

    Topics: Acidosis, Lactic; Amino Acid Metabolism, Inborn Errors; Arginine; Central Nervous System; Creatine; Dietary Supplements; Humans; MELAS Syndrome; Mitochondrial Myopathies; Nitric Oxide; Vascular Diseases

2008

Other Studies

4 other study(ies) available for arginine and Luft Disease

ArticleYear
[Expression of long chain fatty acid oxidase in maternal and fetal tissues in preeclampsia-like mouse model in mid-gestation].
    Zhonghua yi xue za zhi, 2015, Jan-06, Volume: 95, Issue:1

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Animals; Arginine; Cardiomyopathies; Disease Models, Animal; Fatty Acids; Female; Fetal Development; Fetus; Humans; Lipid Metabolism, Inborn Errors; Liver; Mice; Mice, Inbred C57BL; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Oxidation-Reduction; Oxidoreductases; Placenta; Pre-Eclampsia; Pregnancy; Rhabdomyolysis

2015
Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emia.
    Internal medicine (Tokyo, Japan), 2015, Volume: 54, Issue:24

    Topics: Adult; Aged; Arginine; Creatine Kinase; Electrons; Female; Humans; Male; Mitochondria; Mitochondrial Myopathies; Muscle Weakness; Myalgia

2015
[Variation of long-chain 3-hydroxyacyl-CoA dehydrogenase DNA methylation in placenta of different preeclampsia-like mouse models].
    Zhonghua fu chan ke za zhi, 2015, Volume: 50, Issue:10

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; 3-Hydroxyacyl-CoA Dehydrogenase; Animals; Arginine; Cardiomyopathies; Disease Models, Animal; DNA Methylation; Fatty Acids; Female; Humans; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mice; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Oxidation-Reduction; Oxidative Stress; Placenta; Pre-Eclampsia; Pregnancy; Rhabdomyolysis

2015
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