Compounds > 3-methylglutaconic acid

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3-methylglutaconic acid and Acidosis, Lactic

3-methylglutaconic acid has been researched along with Acidosis, Lactic in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	4 (57.14)	18.2507
2000's	1 (14.29)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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, RJ	1
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I	1
Greter, J; Holme, E; Jacobson, CE; Larsson, NG; Lindstedt, S; Nilsson, KO; Oldfors, A; Tulinius, M	1
Bennett, MJ; Gibson, KM; Jakobs, C; Lichter-Konecki, U; Mize, CE; Munnich, A; Rotig, A; Trefz, FK	1
Amir, N; Barash, V; Elpeleg, ON; Hurwitz, Y; Meiron, D; Tal, I	1
Brown, GK; Haan, EA; Pitt, JJ; Scholem, RD; Wraith, JE	1
Cartigny, B; Dubos, JP; Farriaux, JP; Gibson, KM; Largilliere, C; Nuyts, JP; Vallee, L	1

Other Studies

7 other study(ies) available for 3-methylglutaconic acid and Acidosis, Lactic

Article	Year
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
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects. The Journal of pediatrics, 1992, Volume: 121, Issue:6 Topics: Acidosis, Lactic; Anemia, Aplastic; Biomarkers; Child, Preschool; DNA, Mitochondrial; Electron Transport; Female; Gene Deletion; Glutarates; Humans; Hydro-Lyases; Infant; Male; Mitochondria; Neutropenia; Syndrome; Thrombocytopenia	1992
3-Methylglutaconic aciduria with persistent metabolic acidosis and 'uncoupling episodes'. Journal of inherited metabolic disease, 1990, Volume: 13, Issue:2 Topics: Acidosis; Acidosis, Lactic; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Food, Formulated; Glutarates; Humans; Male; Mitochondria, Muscle	1990
Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria. European journal of pediatrics, 1987, Volume: 146, Issue:5 Topics: Abnormalities, Multiple; Acidosis; Acidosis, Lactic; Child, Preschool; Citric Acid Cycle; Follow-Up Studies; Glutarates; Humans; Infant; Male; Meglutol; Virus Diseases	1987
3-Methylglutaconic aciduria: neonatal onset with lactic acidosis. Journal of inherited metabolic disease, 1989, Volume: 12, Issue:3 Topics: Acidosis, Lactic; Amino Acid Metabolism, Inborn Errors; Female; Glutarates; Humans; Infant, Newborn	1989