urea has been researched along with Glycogen Storage Disease Type I in 3 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Some inborn errors of metabolism respond to vitamin therapy." | 2.38 | Nutritional therapy for selected inborn errors of metabolism. ( Levy, HL, 1989) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Morris, AA | 1 |
| Leonard, JV | 1 |
| Ekert, H | 1 |
| Waters, KD | 1 |
| Levy, HL | 1 |
2 reviews available for urea and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Early recognition of metabolic decompensation.
Topics: Biomarkers; Brain Diseases, Metabolic; Child; Fatty Acids; Glycogen Storage Disease Type I; Humans; | 1997 |
Nutritional therapy for selected inborn errors of metabolism.
Topics: Glycogen Storage Disease Type I; Humans; Metabolism, Inborn Errors; Microbodies; Multiple Carboxylas | 1989 |
1 other study available for urea and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Hematologic emergencies in children.
Topics: Acute Disease; Acute Kidney Injury; Adolescent; Anemia, Aplastic; Anemia, Hemolytic, Autoimmune; Asp | 1978 |