biotin has been researched along with Fatty Liver with Encephalopathy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Bergstrøm, T; Greter, J; Levin, AH; Steen, G; Tryding, N; Wass, U | 1 |
| Bartlett, K; Layward, EM; Pollitt, RJ; Tanner, MS | 1 |
2 other study(ies) available for biotin and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
Propionyl-CoA carboxylase deficiency: case report, effect of low-protein diet and identification of 3-oxo-2-methylvaleric acid 3-hydroxy-2-methylvaleric acid, and maleic acid in urine.
Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Caproates; Carboxy-Lyases; Dietary Proteins; Female; Humans; Hydroxy Acids; Infant; Infant, Newborn; Keto Acids; Leukocytes; Maleates; Methylmalonyl-CoA Decarboxylase; Pentanoic Acids; Propionates; Reye Syndrome; Valerates | 1981 |
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness.
Topics: Biotin; Drug Resistance; Humans; Infant; Male; Oxo-Acid-Lyases; Reye Syndrome | 1989 |