Compounds > aspartic acid
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aspartic acid and Developmental Psychomotor Disorders

aspartic acid has been researched along with Developmental Psychomotor Disorders in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's3 (42.86)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
Barbaro, M; Jonsson, M; Kucinski, T; Lasorsa, FM; Naess, K; Palmieri, F; Pierri, CL; Sterky, FH; Töhönen, V; Wedell, A; Wibom, R1
Casarejos, MJ; Contreras, L; Dierssen, M; Grau, JM; Llorente-Folch, I; Mena, MA; Pardo, B; Saheki, T; Sahún, I; Satrústegui, J1
Bodensteiner, JB; Johnsen, SD; Kerrigan, JF1
Isenberg, JN; Sharp, HL1
de Groot, CJ; Hommes, FA1

Other Studies

7 other study(ies) available for aspartic acid and Developmental Psychomotor Disorders

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
AGC1 deficiency associated with global cerebral hypomyelination.
    The New England journal of medicine, 2009, Jul-30, Volume: 361, Issue:5

    Topics: Amino Acid Transport Systems, Acidic; Antiporters; Aspartic Acid; Cerebrum; Child, Preschool; Epilepsy; Female; Hereditary Central Nervous System Demyelinating Diseases; Homozygote; Humans; Magnetic Resonance Imaging; Mitochondria; Mitochondrial Membrane Transport Proteins; Muscle Hypotonia; Mutation, Missense; Protein Isoforms; Psychomotor Disorders; Sequence Analysis, DNA; Syndrome

2009
AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway.
    Journal of neurochemistry, 2013, Volume: 124, Issue:3

    Topics: Amino Acid Transport Systems, Acidic; Animals; Antiporters; Aspartic Acid; Corpus Striatum; Dopamine; Emotions; Exploratory Behavior; Female; Hereditary Central Nervous System Demyelinating Diseases; Malates; Male; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Motor Skills Disorders; Neural Pathways; Oxidative Stress; Pregnancy; Psychomotor Disorders; Substantia Nigra

2013
Leukoencephalopathy with bilateral anterior temporal lobe cysts.
    Journal of child neurology, 2006, Volume: 21, Issue:5

    Topics: Adolescent; Aspartic Acid; Brain Neoplasms; Central Nervous System Cysts; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Inositol; Intellectual Disability; Male; Psychomotor Disorders; Retrospective Studies; Temporal Lobe

2006
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis.
    The Journal of pediatrics, 1975, Volume: 86, Issue:5

    Topics: Amidohydrolases; Aminoglycosides; Aspartic Acid; Child, Preschool; Chromatography, Thin Layer; Cleidocranial Dysplasia; Diagnosis, Differential; Facial Expression; Female; Glucosamine; Hepatomegaly; Humans; Joint Diseases; Leukocytes; Lymphocytes; Mass Screening; Metabolism, Inborn Errors; Mucopolysaccharidoses; Psychomotor Disorders; Splenomegaly; Vacuoles

1975
Further speculation on the pathogenesis of Leigh's encephalomyelopathy.
    The Journal of pediatrics, 1973, Volume: 82, Issue:3

    Topics: Aspartic Acid; Brain Stem; Citric Acid Cycle; Encephalomalacia; Humans; Intellectual Disability; Ligases; Metabolism, Inborn Errors; Psychomotor Disorders; Syndrome; Thiamine

1973