adipic acid has been researched along with ethylmalonic acid in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (41.67) | 18.7374 |
| 1990's | 7 (58.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boutron, A; Brivet, M; Haengeli, CA; Khellaf, A; Lemonnier, A; Rocchiccioli, F; Tardieu, M | 1 |
| de Sousa, C; Green, A; Pollitt, RJ; Preece, MA | 1 |
| Gargus, JJ; O'Shea, JJ; Previs, SF; Rinaldo, P; Schmidt-Sommerfeld, E; Welch, RD; Zinn, AB | 1 |
| Charpentier, C; Harpey, JP; Paturneau-Jouas, M | 1 |
| Amendt, BA; Cloherty, J; Greene, C; Moon, A; Rhead, WJ; Shih, V; Sweetman, L; Teel, L | 1 |
| Amendt, BA; Rhead, WJ | 2 |
| Ikeda, Y; Keese, SM; Tanaka, K | 1 |
| Sherwood, WG; Verjee, ZH | 1 |
| Ballard, CG; Handy, S; McGibben, L; Mohan, RN; Silveira, WR | 1 |
| Elias, E; Gray, RG; Green, A; Poulton, K | 1 |
| Geiger, R; Lehnert, W; Rhead, W; Sperl, W | 1 |
1 review(s) available for adipic acid and ethylmalonic acid
| Article | Year |
|---|---|
Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.
Topics: Adipates; Adolescent; Carnitine; Child; Child, Preschool; Fatty Acid Desaturases; Fatty Acids; Humans; Infant; Lipid Metabolism, Inborn Errors; Malonates; Oxidation-Reduction; Sudden Infant Death | 1990 |
11 other study(ies) available for adipic acid and ethylmalonic acid
| Article | Year |
|---|---|
Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adipates; Brain Diseases; Fatty Acids; Female; Fibroblasts; Humans; Infant; Liver Cirrhosis; Malonates; Metabolism, Inborn Errors; Muscular Diseases; Myristic Acid; Myristic Acids; Oxidation-Reduction; Palmitic Acid; Palmitic Acids; Riboflavin | 1991 |
Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).
Topics: Acyl-CoA Dehydrogenases; Adipates; Carnitine; Child; Humans; Hypoglycemia; Male; Malonates; Riboflavin | 1991 |
Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines.
Topics: Acylation; Adipates; Administration, Oral; Carnitine; Child; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Female; Glycine; Humans; Iron-Sulfur Proteins; Malonates; Metabolism, Inborn Errors; Multienzyme Complexes; Oxidoreductases Acting on CH-NH Group Donors; Triglycerides | 1991 |
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients.
Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenases; Adipates; Adult; Butyrates; Butyric Acid; Female; Fibroblasts; Humans; Hydroxybutyrates; Lactates; Lactic Acid; Lipid Metabolism, Inborn Errors; Malonates; Succinates | 1987 |
The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Adipates; Animals; Caprylates; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Fibroblasts; Flavin-Adenine Dinucleotide; Flavoproteins; Glutarates; Lipid Metabolism, Inborn Errors; Liver; Malonates; Mitochondria; Palmitoyl Coenzyme A; Succinates; Succinic Acid; Swine | 1986 |
Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.
Topics: Adipates; Animals; Carbohydrate Metabolism, Inborn Errors; Cell-Free System; Cycloheximide; Electron-Transferring Flavoproteins; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Flavoproteins; Glutarates; Malonates; Molecular Weight; Protein Processing, Post-Translational; Rabbits; Rhodamines | 1986 |
Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment.
Topics: Acyl-CoA Dehydrogenases; Adipates; Female; Humans; Infant; Malonates | 1985 |
Electron-transferring flavoprotein deficiency in the multiple acyl-CoA dehydrogenation disorders, glutaric aciduria type II and ethylmalonic--adipic aciduria.
Topics: Adipates; Fatty Acid Desaturases; Female; Glutarates; Humans; Male; Malonates | 1984 |
Eating disorder in a 6-year-old Asian girl with ethyl malonic adipic aciduria.
Topics: Acculturation; Adipates; Anorexia Nervosa; Asia; Child; Combined Modality Therapy; England; Ethnicity; Failure to Thrive; Family; Family Therapy; Fatty Acid Desaturases; Female; Humans; Malonates; Personality Assessment | 1993 |
Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.
Topics: Adipates; Adult; Humans; Lipid Metabolism, Inborn Errors; Liver Diseases; Male; Malonates; Muscular Diseases; Reye Syndrome | 1997 |
Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
Topics: Adipates; Child; Child, Preschool; Fatty Acid Desaturases; Fibroblasts; Follow-Up Studies; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Male; Malonates; Mitochondrial Myopathies; Muscle Hypotonia; Respiratory Sounds; Riboflavin | 1997 |