lactulose has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 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 | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Ahmed, A; Ata, F; Gaber, M; Hashim, A; Mahfouz, A; Musa, S; Petkar, M; Schirmacher, P | 1 |
| Bakker, HD; Brink, M; de Bree, PK; Desplanque, J; van der Heiden, C; Wadman, SK | 1 |
| Glasgow, AM; Kraegel, JH; Schulman, JD | 1 |
1 review(s) available for lactulose and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
Refractory Hyperammonemic encephalopathy in Fibrolamellar hepatocellular carcinoma, a case report and literature review.
Topics: Adult; Ammonia; Carcinoma, Hepatocellular; Humans; Lactulose; Liver Neoplasms; Male; Ornithine Carbamoyltransferase Deficiency Disease | 2022 |
2 other study(ies) available for lactulose and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Child, Preschool; Citrates; Dietary Proteins; Humans; Lactulose; Male; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease | 1978 |
Studies of the cause and treatment of hyperammonemia in females with ornithine transcarbamylase deficiency.
Topics: Amino Acids, Essential; Ammonia; Child; Dietary Proteins; Female; Heterozygote; Humans; Keto Acids; Lactulose; Liver; Ornithine Carbamoyltransferase Deficiency Disease; X Chromosome | 1978 |