lysine has been researched along with Glycogen Storage Disease Type I in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baynes, JW; den Hollander, NC; Graaff, R; Mulder, DJ; Smit, AJ; Smit, GP; Thorpe, SR | 1 |
| Elleder, M; Francová, H; Hrabincová, E; Kozák, L; Pesková, K; Stastná, S | 1 |
2 other study(ies) available for lysine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Advanced glycation end products and the absence of premature atherosclerosis in glycogen storage disease Ia.
Topics: Adolescent; Adult; Arginine; Atherosclerosis; Carotid Arteries; Collagen; Female; Glycation End Products, Advanced; Glycogen Storage Disease Type I; Humans; Lysine; Male; Oxidative Stress; Risk; Skin; Tunica Intima; Tunica Media | 2007 |
Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type ia, including novel mutations K76N, V166A and 540del5.
Topics: Alanine; Amino Acid Substitution; Asparagine; Czech Republic; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Humans; Lysine; Mutation; Sequence Deletion; Slovakia; Valine | 2000 |