ethylmalonic acid has been researched along with riboflavin in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 1 (14.29) | 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 |
| Bennett, MJ; Gray, RG; Green, A; Marshall, TG; Pollitt, RJ | 1 |
| Geiger, R; Lehnert, W; Rhead, W; Sperl, W | 1 |
| Ahn, YM; Eun, BL; Hahn, SH; Jang, SH; Lee, EH; Rinaldo, P; Ryu, KH; Shin, YJ; Yamaguchi, S; Yoon, HR | 1 |
| Duran, M; Hogeveen, M; Ijlst, L; Niezen-Koning, KE; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA | 1 |
| Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA | 1 |
2 trial(s) available for ethylmalonic acid and riboflavin
| Article | Year |
|---|---|
Therapeutic trial in the first three Asian cases of ethylmalonic encephalopathy: response to riboflavin.
Topics: Brain Diseases, Metabolic, Inborn; Child, Preschool; Coenzymes; Cognition; Diarrhea; Electron Transport; Female; Humans; Infant; Korea; Malonates; Motor Skills; Riboflavin; Syndrome; Ubiquinone | 2001 |
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.
Topics: Adolescent; Biomarkers; Butyryl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Female; Flavin-Adenine Dinucleotide; Genetic Predisposition to Disease; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Malonates; Mutation; Phenotype; Prospective Studies; Riboflavin; Treatment Outcome; Vitamin B Complex | 2010 |
5 other study(ies) available for ethylmalonic acid and riboflavin
| 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 |
Riboflavin-responsive ethylmalonic-adipic aciduria.
Topics: Adipates; Butyrates; Cells, Cultured; Fibroblasts; Humans; Infant; Male; Malonates; Metabolism, Inborn Errors; Riboflavin | 1985 |
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 |
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Carnitine; Child; Child, Preschool; Female; Genotype; Humans; Infant; Infant, Newborn; Male; Malonates; Metabolism, Inborn Errors; Mutation; Neonatal Screening; Netherlands; Phenotype; Retrospective Studies; Riboflavin; Vitamin B Complex | 2006 |