Compounds > 3-methylglutaric acid
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3-methylglutaric acid and Inborn Errors of Metabolism

3-methylglutaric acid has been researched along with Inborn Errors of Metabolism in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's2 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anikster, Y; Ben-Zeev, B; Blumkin, L; Hassin-Baer, S; Lerman-Sagie, T; Lev, D; Schweiger, A; Sofer, S; Yahalom, G1
Hagberg, B; Hjalmarson, O; Lindstedt, S; Ransnäs, L; Steen, G1
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I1
Chemke, J; Chitayat, D; Gibson, KM; Kronick, JB; Mamer, OA; McGill, JJ; Rosenblatt, B; Scriver, CR; Sweetman, L1

Other Studies

4 other study(ies) available for 3-methylglutaric acid and Inborn Errors of Metabolism

ArticleYear
The neuropsychological profile of patients with 3-methylglutaconic aciduria type III, Costeff syndrome.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2015, Volume: 168B, Issue:3

    Topics: Adult; Chorea; Cognition Disorders; Executive Function; Female; Follow-Up Studies; Humans; Intelligence; Male; Meglutol; Memory, Short-Term; Metabolism, Inborn Errors; Middle Aged; Neuropsychological Tests; Optic Atrophy; Prognosis; Psychomotor Performance; Spastic Paraplegia, Hereditary; Young Adult

2015
3-Methylglutaconic aciduria in two infants.
    Clinica chimica acta; international journal of clinical chemistry, 1983, Oct-31, Volume: 134, Issue:1-2

    Topics: Creatinine; Female; Fibroblasts; Glutarates; Hemiterpenes; Humans; Hydroxymethylglutaryl-CoA Synthase; Infant; Leucine; Leukocytes; Meglutol; Metabolism, Inborn Errors; Pentanoic Acids

1983
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.
    European journal of pediatrics, 1993, Volume: 152, Issue:8

    Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; Electron Transport Complex IV; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Male; Meglutol; Metabolism, Inborn Errors; Mitochondrial Myopathies; Respiration Disorders

1993
3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4').
    Journal of inherited metabolic disease, 1992, Volume: 15, Issue:2

    Topics: Amniotic Fluid; Child; Female; Fibroblasts; Glutarates; Humans; Hydro-Lyases; Male; Meglutol; Metabolism, Inborn Errors; Pregnancy; Prenatal Diagnosis

1992