serine has been researched along with Glycogen Storage Disease Type I in 1 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hornemann, T | 1 |
| Alecu, I | 1 |
| Hagenbuch, N | 1 |
| Zhakupova, A | 1 |
| Cremonesi, A | 1 |
| Gautschi, M | 1 |
| Jung, HH | 1 |
| Meienberg, F | 1 |
| Bilz, S | 1 |
| Christ, E | 1 |
| Baumgartner, MR | 1 |
| Hochuli, M | 1 |
1 other study available for serine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Disturbed sphingolipid metabolism with elevated 1-deoxysphingolipids in glycogen storage disease type I - A link to metabolic control.
Topics: Adolescent; Adult; Alanine; Female; Glucose; Glycogen Storage Disease Type I; Humans; Lipid Metaboli | 2018 |