Page last updated: 2024-08-26

3-methylglutaconic acid and Cardiomyopathy, Hypertrophic

3-methylglutaconic acid has been researched along with Cardiomyopathy, Hypertrophic in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Bertini, E; Boenzi, S; Carrozzo, R; D'Amico, A; Deodato, F; Di Rosa, G; Dionisi-Vici, C; Loupatty, FJ; Maiorana, A; Rizzo, C; Santorelli, FM; Tozzi, G; Wanders, RJ1
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I1
Greter, J; Holme, E; Jacobson, CE; Larsson, NG; Lindstedt, S; Nilsson, KO; Oldfors, A; Tulinius, M1
Andrieu, A; Bildstein, G; Chateauneuf, R; Delisle, B; Divry, P; Laurent-Pellegrin, M; Netter, JC; Petrus, M1

Other Studies

4 other study(ies) available for 3-methylglutaconic acid and Cardiomyopathy, Hypertrophic

ArticleYear
Hypertrophic cardiomyopathy, cataract, developmental delay, lactic acidosis: a novel subtype of 3-methylglutaconic aciduria.
    Journal of inherited metabolic disease, 2006, Volume: 29, Issue:4

    Topics: Acidosis, Lactic; Amino Acid Metabolism, Inborn Errors; Brain; Cardiomyopathy, Hypertrophic; Cataract; Developmental Disabilities; Family Health; Female; Glutarates; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Pedigree

2006
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
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria.
    Pediatric research, 1992, Volume: 32, Issue:6

    Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; DNA Mutational Analysis; DNA, Mitochondrial; Female; Glutarates; Humans; Infant; Metabolism, Inborn Errors; Mitochondria, Muscle; Proton-Translocating ATPases

1992
[Hypertrophic cardiomyopathy and neonatal encephalopathy associated with 3-methylglutaconic aciduria].
    Annales de pediatrie, 1987, Volume: 34, Issue:9

    Topics: Autopsy; Brain Diseases; Cardiomyopathy, Hypertrophic; Female; Glutarates; Humans; Infant, Newborn; Myocardium; Occipital Lobe

1987