Compounds > glutamic acid

glutamic acid and External Ophthalmoplegia

glutamic acid has been researched along with External Ophthalmoplegia 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
Andrews, C; Balasubramanian, R; Chan, WM; Chew, S; Engle, EC; Kang, PB; MacKinnon, SE1
Brusco, A; Cagnoli, C; Di Bella, D; Di Donato, S; Gellera, C; Mariotti, C; Seri, M; Taroni, F1
Berkovic, SF; Byrne, E; Dennett, X; Marzuki, S; Mastaglia, F; Sudoyo, H; Trounce, I1

Other Studies

3 other study(ies) available for glutamic acid and External Ophthalmoplegia

ArticleYear
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome.
    The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3

    Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Developmental Disabilities; Endocrine System Diseases; Eye Diseases, Hereditary; Female; Fibrosis; Glutamic Acid; Humans; Kallmann Syndrome; Lysine; Male; Ophthalmoplegia; Pedigree; Phenotype; Syndrome; Tubulin

2015
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
    Cerebellum (London, England), 2008, Volume: 7, Issue:2

    Topics: Adolescent; Adult; Aged; Base Sequence; Brain; Child; Chromosome Mapping; Chromosomes, Human, Pair 18; Female; Genes, Dominant; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Ophthalmoplegia; Pedigree; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spinocerebellar Ataxias; Young Adult

2008
Functional respiratory chain studies in subjects with chronic progressive external ophthalmoplegia and large heteroplasmic mitochondrial DNA deletions.
    Journal of the neurological sciences, 1991, Volume: 102, Issue:1

    Topics: Adult; Chromosome Deletion; Cytochrome-c Oxidase Deficiency; DNA, Mitochondrial; Electron Transport; Electron Transport Complex III; Electron Transport Complex IV; Female; Glutamates; Glutamic Acid; Humans; Male; Middle Aged; Mitochondria; NAD(P)H Dehydrogenase (Quinone); Ophthalmoplegia; Oxidative Phosphorylation; Oxygen Consumption; Pyruvates; Pyruvic Acid; Quinone Reductases; RNA, Transfer; Succinates; Succinic Acid

1991