gemfibrozil has been researched along with Glycogen Storage Disease Type I in 1 studies
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 |
---|---|---|
"Because the complications of hyperlipidemia are caused mainly by TC, thereby, by maintaining it at a normal level, we could set a TG target by the linear equation that allowed a certain degree of hypertriglyceridemia." | 1.56 | Lipid status and linear relationship between total cholesterol and triglycerides in glycogen storage disease type I. ( Hong, YH; Ma, MS; Qiu, ZQ; Sun, ZX; Wei, M; Xu, YW; Yuan, YH; Zhang, ZJ, 2020) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 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 | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Zhang, ZJ | 1 |
Yuan, YH | 1 |
Ma, MS | 1 |
Hong, YH | 1 |
Sun, ZX | 1 |
Xu, YW | 1 |
Wei, M | 1 |
Qiu, ZQ | 1 |
1 other study available for gemfibrozil and Glycogen Storage Disease Type I
Article | Year |
---|---|
Lipid status and linear relationship between total cholesterol and triglycerides in glycogen storage disease type I.
Topics: Adolescent; Adult; Child; Child, Preschool; Cholesterol; Female; Fenofibrate; Gemfibrozil; Glucose-6 | 2020 |