phenylalanine has been researched along with Glycogen Storage Disease Type I in 1 studies
| 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 |
|---|---|
| Boemer, F; Debray, FG; Gersting, SW; Goffette, P; Goyens, P; Jazouli, N; Menten, R; Muntau, AC; Najimi, M; Sana, G; Schoos, R; Smets, F; Sokal, EM; Stéphenne, X; Tondreau, T | 1 |
1 other study(ies) available for phenylalanine and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Hepatocyte transplantation using the domino concept in a child with tetrabiopterin nonresponsive phenylketonuria.
Topics: Cell- and Tissue-Based Therapy; Child; Female; Glycogen Storage Disease Type I; Half-Life; Hepatocytes; Humans; Infant; Liver Function Tests; Male; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias | 2012 |