serine has been researched along with Glycogen Storage Disease 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: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Laforêt, P | 1 |
| Richard, P | 1 |
| Said, MA | 1 |
| Romero, NB | 1 |
| Lacene, E | 1 |
| Leroy, JP | 1 |
| Baussan, C | 1 |
| Hogrel, JY | 1 |
| Lavergne, T | 1 |
| Wahbi, K | 1 |
| Hainque, B | 1 |
| Duboc, D | 1 |
1 other study available for serine and Glycogen Storage Disease
| Article | Year |
|---|---|
A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.
Topics: Adult; AMP-Activated Protein Kinases; Cardiomyopathy, Hypertrophic; DNA Mutational Analysis; Exercis | 2006 |