Compounds > meglutol

meglutol and leucine

meglutol has been researched along with leucine in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	6 (46.15)	18.7374
1990's	4 (30.77)	18.2507
2000's	2 (15.38)	29.6817
2010's	1 (7.69)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gibson, KM; Lee, CF; Wappner, RS	1
Chalmers, RA; Halliday, D; Thompson, GN	1
Buchanan, D; Dasouki, M; Gibson, KM; Mercer, N; Thoene, J	1
Cann, HM; Gibson, KM; Greene, CL; Holm, J; Nyhan, WL; Robinson, BH; Sweetman, L	1
Bechinger, D; Leupold, D; Lisson, G; Wallesch, C	1
Beemer, FA; Bruinvis, L; Duran, M; Ketting, D; Tibosch, AS; Wadman, SK	1
Hagberg, B; Hjalmarson, O; Lindstedt, S; Ransnäs, L; Steen, G	1
Berry, HK; Denton, MD; Norman, EJ	1
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I	1
Yoshida, I	1
Casals, N; Hegardt, FG; Pie, J; Puisac, B	1
Engelke, UF; Kluijtmans, LA; Kremer, B; Loss, S; Loupatty, FJ; Morava, E; Moskau, D; van den Bergh, E; van der Graaf, M; Wanders, RJ; Wevers, RA	1
Acquaviva, C; Caruba, C; Giudicelli, H; Khalfi, A; Moreigne, M; Pierron, S; Rolland, MO; Touati, G	1

Reviews

1 review(s) available for meglutol and leucine

Article	Year
[3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency]. Ryoikibetsu shokogun shirizu, 1998, Issue:18 Pt 1 Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Humans; Leucine; Meglutol; Mutation; Prognosis	1998

Other Studies

12 other study(ies) available for meglutol and leucine

Article	Year
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:3 Topics: Carnitine; Diseases in Twins; Fibroblasts; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Lymphocytes; Male; Meglutol	1992
The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria. European journal of pediatrics, 1990, Volume: 149, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child; Diseases in Twins; Female; Glutarates; Humans; Leucine; Male; Meglutol; Oxo-Acid-Lyases; Phenylalanine; Proteins; Valerates	1990
3-Hydroxy-3-methylglutaric aciduria: response to carnitine therapy and fat and leucine restriction. Journal of inherited metabolic disease, 1987, Volume: 10, Issue:2 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carnitine; Dietary Fats; Dietary Proteins; Female; Glutarates; Humans; Infant, Newborn; Leucine; Meglutol; Oxo-Acid-Lyases	1987
3-Hydroxy-3-methylglutaric aciduria. Journal of neurogenetics, 1984, Volume: 1, Issue:2 Topics: Cells, Cultured; Female; Fibroblasts; Follow-Up Studies; Glutarates; Humans; Infant, Newborn; Leucine; Meglutol; Oxo-Acid-Lyases; Skin; Valerates	1984
CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase. Neuroradiology, 1981, Volume: 22, Issue:2 Topics: Acyl Coenzyme A; Brain Diseases; Female; Humans; Infant, Newborn; Leucine; Meglutol; Oxo-Acid-Lyases; Tomography, X-Ray Computed	1981
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism. The Journal of pediatrics, 1982, Volume: 101, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Glutarates; Humans; Hydro-Lyases; Leucine; Male; Meglutol; Speech Disorders; Valerates	1982
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
Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousins. Clinical chemistry, 1982, Volume: 28, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Hydroxy Acids; Infant; Leucine; Male; Meglutol; Oxo-Acid-Lyases; Valerates	1982
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
Molecular basis of 3-hydroxy-3-methylglutaric aciduria. Journal of physiology and biochemistry, 2003, Volume: 59, Issue:4 Topics: Alternative Splicing; Chromosomes, Human, Pair 1; DNA Mutational Analysis; Exons; Genotype; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Leucine; Meglutol; Mitochondria; Mutation; Oxo-Acid-Lyases; Phenotype; Polymorphism, Genetic	2003
NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism. NMR in biomedicine, 2006, Volume: 19, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Brain; Female; Glutarates; Humans; Leucine; Magnetic Resonance Spectroscopy; Meglutol; Middle Aged; Valerates	2006
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2010, Volume: 17, Issue:1 Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Chromosome Aberrations; Combined Modality Therapy; Diet, Protein-Restricted; DNA Mutational Analysis; Exons; Genes, Recessive; Humans; Hypoglycemia; Leucine; Male; Meglutol; Oxo-Acid-Lyases; Polymerase Chain Reaction; Rare Diseases; Sequence Analysis, DNA	2010