carbamyl phosphate has been researched along with Glycogen Storage Disease Type I in 2 studies
Carbamyl Phosphate: The monoanhydride of carbamic acid with PHOSPHORIC ACID. It is an important intermediate metabolite and is synthesized enzymatically by CARBAMYL-PHOSPHATE SYNTHASE (AMMONIA) and CARBAMOYL-PHOSPHATE SYNTHASE (GLUTAMINE-HYDROLYZING).
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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Arion, WJ | 1 |
| Canfield, WK | 1 |
| Hefferan, PM | 1 |
| Howell, RR | 1 |
1 review available for carbamyl phosphate and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Glucose-6-phosphatase and type 1 glycogen storage disease: some critical considerations.
Topics: Animals; Biological Transport; Carbamyl Phosphate; Diphosphates; Endoplasmic Reticulum; Glucose-6-Ph | 1993 |
1 other study available for carbamyl phosphate and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Genetic evidence for the common identity of glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase.
Topics: Carbamyl Phosphate; Diphosphates; Glucose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; H | 1977 |