Compounds > 3-methylglutaconic acid
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3-methylglutaconic acid and Leigh Disease

3-methylglutaconic acid has been researched along with Leigh Disease in 5 studies

Research

Studies (5)

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

Authors

AuthorsStudies
Duszynski, J; Jurkiewicz, E; Karkucinska-Wieckowska, A; Lebiedzinska, M; Pajdowska, M; Pinton, P; Pronicka, E; Pronicki, M; Suski, J; Szymanska-Debinska, T; Trubicka, J; Wieckowski, MR1
de Koning, T; Engelke, U; Huizing, M; Kluijtmans, LA; Loupatty, FJ; Morava, E; Rodenburg, RJ; Smeitink, JA; Wevers, R; Wortmann, S1
Campos-Castelló, J; Cortés, BM; Fernández-Mayoralas, DM; Jareño, NM; Pérez, MU; Silvestre, CP1
Broide, E; Elpeleg, O; Lahat, E1
Borrone, C; Caruso, U; Di Rocco, M; Fantasia, AR; Gibson, KM; Lamantea, E; Lupino, S; Moroni, I1

Other Studies

5 other study(ies) available for 3-methylglutaconic acid and Leigh Disease

ArticleYear
Increased reactive oxygen species (ROS) production and low catalase level in fibroblasts of a girl with MEGDEL association (Leigh syndrome, deafness, 3-methylglutaconic aciduria).
    Folia neuropathologica, 2011, Volume: 49, Issue:1

    Topics: Catalase; Child, Preschool; Deafness; Female; Fibroblasts; Glutarates; Hearing Loss, Sensorineural; Humans; Leigh Disease; Mitochondrial Diseases; Reactive Oxygen Species

2011
Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation.
    Molecular genetics and metabolism, 2006, Volume: 88, Issue:1

    Topics: Adolescent; Brain Diseases, Metabolic; Child; Child, Preschool; Consanguinity; Fatal Outcome; Female; Glutarates; Hearing Loss, Sensorineural; Humans; Infant, Newborn; Leigh Disease; Male; Mitochondrial Diseases; Oxidative Phosphorylation; Syndrome; Valerates

2006
3-methylglutaconic aciduria type 4 manifesting as Leigh syndrome in 2 siblings.
    Journal of child neurology, 2007, Volume: 22, Issue:2

    Topics: Brain Diseases, Metabolic; Child, Preschool; Female; Glutarates; Humans; Infant; Leigh Disease; Magnetic Resonance Imaging; Male; Siblings

2007
Type IV 3-methylglutaconic (3-MGC) aciduria: a new case presenting with hepatic dysfunction.
    Pediatric neurology, 1997, Volume: 17, Issue:4

    Topics: Diagnosis, Differential; Disease Progression; Glutarates; Humans; Infant; Leigh Disease; Liver Diseases; Magnetic Resonance Imaging; Male; Nervous System Diseases

1997
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease.
    Journal of inherited metabolic disease, 1999, Volume: 22, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Glutarates; Humans; Leigh Disease; Male; Methionine; Skull; Tomography, X-Ray Computed

1999