glycine has been researched along with Deficiency, Glucosephosphatase in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Glycogen storage disease type 1a (von Gierke disease, GSD1a) is caused by the deficiency of microsomal glucose-6-phosphatase (G6Pase) activity." | 1.30 | Glycogen storage disease type 1a in three siblings with the G270V mutation. ( Isam, J; Moses, SW; Parvari, R, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sartorato, EL | 1 |
| Reis, FC | 1 |
| Norato, DY | 1 |
| Hackel, C | 1 |
| Parvari, R | 1 |
| Isam, J | 1 |
| Moses, SW | 1 |
| Stormont, D | 1 |
| Davies, C | 1 |
| Emmerson, BT | 1 |
| Benke, PJ | 1 |
| Gold, S | 1 |
4 other studies available for glycine and Deficiency, Glucosephosphatase
| Article | Year |
|---|---|
A novel mutation in a Brazilian patient with glycogen storage disease type 1a.
Topics: Arginine; Brazil; Glucose-6-Phosphatase; Glycine; Glycogen Storage Disease Type I; Humans; Mutation; | 1998 |
Glycogen storage disease type 1a in three siblings with the G270V mutation.
Topics: Child; Exons; Female; Glucose-6-Phosphatase; Glycine; Glycogen Storage Disease Type I; Humans; Infan | 1999 |
Urate production in heterozygotes for glucose-6-phosphatase deficiency.
Topics: Adult; Blood Platelets; Child, Preschool; Erythrocytes; Female; Glucose-6-Phosphatase; Glucosephosph | 1976 |
Uric acid metabolism in therapy of glycogen storage disease type I.
Topics: Child; Dietary Carbohydrates; Glycine; Glycogen Storage Disease Type I; Humans; Intubation, Gastroin | 1978 |