Compounds > 3-methylglutaconic acid
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3-methylglutaconic acid and Cognition Disorders

3-methylglutaconic acid has been researched along with Cognition Disorders in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eriguchi, M; Hasegawa, Y; Kosugi, M; Kuroda, Y; Kurohara, K; Mizuta, H; Okada, R; Yakushiji, Y; Yamaguchi, S; Yukitake, M1
Henry, AE; Kelly, RI; Mazzocco, MM1
Costeff, H; Elpeleg, ON; Gibson, KM; Joseph, A; Shental, Y; Weitz, R1
Kelley, RI; Mazzocco, MM1

Other Studies

4 other study(ies) available for 3-methylglutaconic acid and Cognition Disorders

ArticleYear
3-Methylglutaconic aciduria type I causes leukoencephalopathy of adult onset.
    Neurology, 2006, Nov-28, Volume: 67, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Cognition Disorders; Dementia, Vascular; DNA Mutational Analysis; Enoyl-CoA Hydratase; Female; Glutarates; Humans; Magnetic Resonance Imaging; Middle Aged; Mutation; Nerve Fibers, Myelinated; Reflex, Abnormal; RNA-Binding Proteins

2006
Barth syndrome is associated with a cognitive phenotype.
    Journal of developmental and behavioral pediatrics : JDBP, 2007, Volume: 28, Issue:1

    Topics: Cardiomyopathy, Dilated; Child; Child, Preschool; Cholesterol; Cognition Disorders; Genotype; Glutarates; Growth Disorders; Humans; Male; Musculoskeletal Diseases; Neuropsychological Tests; Neutropenia; Phenotype; Severity of Illness Index; Syndrome

2007
3-Methylglutaconic aciduria in the Iraqi-Jewish 'optic atrophy plus' (Costeff) syndrome.
    Developmental medicine and child neurology, 1994, Volume: 36, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Cognition Disorders; Female; Glutarates; Humans; Iraq; Jews; Male; Meglutol; Movement Disorders; Optic Atrophy; Syndrome

1994
Preliminary evidence for a cognitive phenotype in Barth syndrome.
    American journal of medical genetics, 2001, Sep-01, Volume: 102, Issue:4

    Topics: Child; Child, Preschool; Cognition Disorders; Female; Genetics, Behavioral; Glutarates; Growth Disorders; Humans; Intelligence Tests; Male; Muscle, Skeletal; Muscular Diseases; Myocardium; Neutropenia; Phenotype; Syndrome

2001