Compounds > arginine

arginine and Chronic Progressive External Ophthalmoplegia

arginine has been researched along with Chronic Progressive External Ophthalmoplegia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Camargos, ST; Cardoso, F; DiMauro, S; Gurgel-Giannetti, J; Hirano, M1
Ceuterick, C; De Jonghe, P; Dehaene, I; Dermaut, B; Löfgren, A; Martin, JJ; Moonen, M; Tack, P; Van Broeckhoven, C; Van Goethem, G; Van Zandijcke, M; Ververken, D; Wibail, A1
Alvarez-Cermeño, JC; Arenas, J; Blázquez, A; Borstein, B; Cabello, A; Campos, Y; Carretero, J; Garesse, R; Gonzalez-Vioque, E; Martín, MA; Rivera, H1

Other Studies

3 other study(ies) available for arginine and Chronic Progressive External Ophthalmoplegia

ArticleYear
POLG1 Arg953Cys mutation: expanded phenotype and recessive inheritance in a Brazilian family.
    Muscle & nerve, 2012, Volume: 45, Issue:3

    Topics: Adult; Arginine; Brazil; Cardiomyopathies; Cysteine; Depression; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electromyography; Female; Gait Disorders, Neurologic; Humans; Male; Muscle, Skeletal; Mutation; Neural Conduction; Ophthalmoplegia, Chronic Progressive External; Parkinson Disease; Phenotype; Succinate Dehydrogenase

2012
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.
    Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:2

    Topics: Adolescent; Adult; Aged; Arginine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electron Transport Complex IV; Female; Genes, Recessive; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Ophthalmoplegia, Chronic Progressive External; Pedigree; Succinate Dehydrogenase; Tryptophan

2003
Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase.
    Neuromuscular disorders : NMD, 2007, Volume: 17, Issue:9-10

    Topics: Aged; Arginine; DNA Helicases; DNA, Mitochondrial; Family Health; Female; Humans; Mitochondrial Proteins; Mutation; Ophthalmoplegia, Chronic Progressive External; Phenotype; Proline; Spain

2007