methionine has been researched along with Acid Alpha-Glucosidase Deficiency in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kim, CM; Kim, DS; Lee, CH; Park, KH; Park, YE | 1 |
| Gieselmann, V; Hasilik, A; Kalsbeek, R; Oude Elferink, R; Steckel, F; Tager, JM; von Figura, K; Waheed, A | 1 |
| Hirschhorn, R; Martiniuk, F; Tzall, S; Zhong, N | 1 |
3 other study(ies) available for methionine and Acid Alpha-Glucosidase Deficiency
| Article | Year |
|---|---|
Two new missense mutations of GAA in late onset glycogen storage disease type II.
Topics: Adult; alpha-Glucosidases; Child; DNA Mutational Analysis; Family Health; Female; Glycogen Storage Disease Type II; Humans; Korea; Lysine; Male; Methionine; Middle Aged; Mutation, Missense; Proline; Serine | 2006 |
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).
Topics: alpha-Glucosidases; Cathepsin D; Cathepsins; Cell Line; Fibroblasts; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Leucine; Methionine; Time Factors | 1982 |
Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele.
Topics: alpha-Glucosidases; Base Sequence; Blotting, Southern; Cell Line; Cloning, Molecular; Endonucleases; Female; Glycogen Storage Disease Type II; Humans; Methionine; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Protein Conformation; Threonine; White People | 1991 |