Compounds > aspartic acid
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aspartic acid and Encephalomyelitis, Subacute Necrotizing

aspartic acid has been researched along with Encephalomyelitis, Subacute Necrotizing in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Beyrath, J; Iannetti, EF; Koopman, WJH; Smeitink, JAM; Willems, PHGM1
Blaser, S; Brudno, M; Foong, J; Miscevic, F; Schmitt, B; Schulze, A1
Baracca, A; Casalena, GA; DiMauro, S; Lenaz, G; Sgarbi, G; Solaini, G1
Brown, GK; Brown, RM; Land, J; Marchington, DR; Matthews, PM; Squier, M1
Maemoto, T; Niimi, H; Sugita, K; Takanashi, J; Tanabe, Y1

Other Studies

5 other study(ies) available for aspartic acid and Encephalomyelitis, Subacute Necrotizing

ArticleYear
Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
    Cell death & disease, 2018, 11-14, Volume: 9, Issue:11

    Topics: Adenosine Triphosphate; Aspartic Acid; Cell Death; Culture Media; Electron Transport Complex I; Fibroblasts; Galactose; Gene Expression; Glycolysis; Humans; Ketoglutaric Acids; Leigh Disease; Malates; Mitochondria; Mitochondrial Diseases; Mutation; NAD; NADH Dehydrogenase; Oxaloacetic Acid; Primary Cell Culture; Pyruvic Acid; Skin

2018
An MRspec database query and visualization engine with applications as a clinical diagnostic and research tool.
    Molecular genetics and metabolism, 2016, Volume: 119, Issue:4

    Topics: Aspartic Acid; Basal Ganglia; Child; Child, Preschool; Choline; Creatine; Female; gamma-Aminobutyric Acid; Humans; Infant; Inositol; Klippel-Feil Syndrome; Leigh Disease; Male; Proton Magnetic Resonance Spectroscopy; White Matter

2016
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy.
    Archives of neurology, 2009, Volume: 66, Issue:8

    Topics: Adenosine Triphosphate; Anti-Infective Agents, Local; Aspartic Acid; C-Reactive Protein; Cell Line; Cell Survival; DNA, Mitochondrial; Energy Metabolism; Gramicidin; Humans; Ketoglutaric Acids; Leigh Disease; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mutation; Nerve Tissue Proteins; Oligomycins; Oxidative Phosphorylation; Retinitis Pigmentosa; Spinocerebellar Degenerations

2009
Molecular genetic characterization of an X-linked form of Leigh's syndrome.
    Annals of neurology, 1993, Volume: 33, Issue:6

    Topics: Amino Acid Sequence; Aspartic Acid; Base Sequence; Brain Stem; Cells, Cultured; Cesarean Section; Citrate (si)-Synthase; DNA; Exons; Fibroblasts; Gestational Age; Humans; Infant, Newborn; Leigh Disease; Leukocytes; Male; Mitochondria, Heart; Mitochondria, Liver; Molecular Sequence Data; Necrosis; Oligodeoxyribonucleotides; Point Mutation; Pyruvate Dehydrogenase Complex; Skin; X Chromosome

1993
Dichloroacetate treatment in Leigh syndrome caused by mitochondrial DNA mutation.
    Journal of the neurological sciences, 1997, Volume: 145, Issue:1

    Topics: Aspartic Acid; Brain; Creatine; Dichloroacetic Acid; DNA, Mitochondrial; Female; Humans; Infant; Lactates; Leigh Disease; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mutation

1997