Compounds > n-acetylaspartic acid
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n-acetylaspartic acid and Central Nervous System Demyelinating Diseases, Hereditary

n-acetylaspartic acid has been researched along with Central Nervous System Demyelinating Diseases, Hereditary in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aoki, I; Barkovich, AJ; Iwasaki, N; Nitta, N; Saito, S; Takanashi, J; Tanaka, R1
Agrimi, G; Castegna, A; Corricelli, M; Danese, A; Fiermonte, G; Giannuzzi, G; Giorgi, C; Lasorsa, FM; Massenzio, F; Monti, B; Palmieri, EM; Palmieri, F; Palmieri, L; Peña-Altamira, LE; Petralla, S; Pinton, P; Porcelli, V; Profilo, E; Sbano, L; Virgili, M; Viscomi, C; Zeviani, M1
Luk, DC; Scheper, GC; van der Knaap, MS; Wong, SS; Wong, VC1
Aaron, S; Gibikote, S; Joseph, E; Sureka, J; Thomas, MM1
Balottin, U; Berardinelli, A; Brunstrom-Hernandez, JE; Collins, CD; Genni, AD; Mita, A; Novara, F; Orcesi, S; Schmidt, JL; Tonduti, D; Triulzi, F; Vanderver, A; Zuffardi, O1
Barker, PB; Bizzi, A; Bugiani, M; Castelli, G; Danesi, U; Erbetta, A; Farina, L; Herskovits, EH; Moroni, I; Uziel, G1

Other Studies

6 other study(ies) available for n-acetylaspartic acid and Central Nervous System Demyelinating Diseases, Hereditary

ArticleYear
Neurochemistry in shiverer mouse depicted on MR spectroscopy.
    Journal of magnetic resonance imaging : JMRI, 2014, Volume: 39, Issue:6

    Topics: Amino Acid Transport Systems, Acidic; Analysis of Variance; Animals; Antiporters; Aspartic Acid; Brain; Cerebral Cortex; Choline; Disease Models, Animal; Hereditary Central Nervous System Demyelinating Diseases; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred ICR; Mice, Neurologic Mutants; Mitochondrial Diseases; Myelin Basic Protein; Neurochemistry; Psychomotor Disorders; Thalamus; White Matter

2014
Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.
    Biochimica et biophysica acta. Molecular basis of disease, 2017, Volume: 1863, Issue:6

    Topics: Amino Acid Transport Systems; Amino Acid Transport Systems, Acidic; Antiporters; Aspartic Acid; Cell Line; Cell Proliferation; Down-Regulation; Hereditary Central Nervous System Demyelinating Diseases; Humans; Mitochondrial Diseases; Mitochondrial Proteins; Neurons; Psychomotor Disorders

2017
Vanishing white matter disease: the first reported chinese patient.
    Journal of child neurology, 2008, Volume: 23, Issue:6

    Topics: Aspartic Acid; Brain; Cerebral Ventricles; Child; Choline; Consanguinity; DNA Mutational Analysis; Eukaryotic Initiation Factor-2B; Female; Genetic Carrier Screening; Genetic Counseling; Genotype; Hereditary Central Nervous System Demyelinating Diseases; Homozygote; Hong Kong; Humans; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Neurologic Examination; Pedigree; Phenotype

2008
Megalencephalic leukoencephalopathy with subcortical cysts in an adult.
    Acta neurologica Belgica, 2009, Volume: 109, Issue:1

    Topics: Aspartic Acid; Central Nervous System Cysts; Cerebrum; Creatine; Diagnostic Imaging; Hereditary Central Nervous System Demyelinating Diseases; Humans; Male; Young Adult

2009
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
    Journal of child neurology, 2013, Volume: 28, Issue:6

    Topics: Aspartic Acid; Basal Ganglia Diseases; Brain; Child, Preschool; Choline; Chromosomes, Human, X; Codon, Nonsense; Developmental Disabilities; DNA Mutational Analysis; Follow-Up Studies; Hereditary Central Nervous System Demyelinating Diseases; Humans; Infant; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Monocarboxylic Acid Transporters; Mutation, Missense; Nerve Fibers, Myelinated; Neurologic Examination; Sex Chromosome Aberrations; Symporters; Thyroid Function Tests

2013
Classification of childhood white matter disorders using proton MR spectroscopic imaging.
    AJNR. American journal of neuroradiology, 2008, Volume: 29, Issue:7

    Topics: Adrenoleukodystrophy; Adult; Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatine; Diagnosis, Differential; DNA Mutational Analysis; Dominance, Cerebral; Female; Hereditary Central Nervous System Demyelinating Diseases; Humans; Image Processing, Computer-Assisted; Infant; Intracellular Signaling Peptides and Proteins; Lactic Acid; Linear Models; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Membrane Proteins; Mitochondrial Diseases; Muscular Dystrophies; Pelizaeus-Merzbacher Disease; Prospective Studies

2008