glutamine 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 |
|---|---|
| Barosa, C; Delgado, TC; Diogo, L; Garcia, P; Jones, JG | 1 |
| Cabral, A; Rocha, H; Vilarinho, L | 1 |
2 other study(ies) available for glutamine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Hepatic anaplerotic outflow fluxes are redirected from gluconeogenesis to lactate synthesis in patients with Type 1a glycogen storage disease.
Topics: Acetyl Coenzyme A; Adolescent; Carbon Isotopes; Child; Citric Acid Cycle; Female; Gluconeogenesis; Glucose; Glucose-6-Phosphatase; Glutamine; Glycerol; Glycogen Storage Disease Type I; Humans; Lactates; Liver; Male; Pyruvic Acid; Young Adult | 2009 |
Identification of a novel nonsense mutation (Q24X) in the glucose-6-phosphatase gene of a Portuguese patient with GSD Ia (von Gierke disease).
Topics: Amino Acid Substitution; Codon, Nonsense; Codon, Terminator; Glucose-6-Phosphatase; Glutamine; Glycogen Storage Disease Type I; Humans; Mutation, Missense; Portugal | 2000 |