lysine has been researched along with Acid beta-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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Horowitz, M; Rapaport, D; Ron, I | 1 |
| Ben-Yoseph, Y; Choy, FY; Humphries, ML | 1 |
| Gardner, LI | 1 |
1 review(s) available for lysine and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Genetically expressed abnormalities in the fetus.
Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12 | 1974 |
2 other study(ies) available for lysine and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease.
Topics: Animals; Cell Line; Gaucher Disease; Glucosylceramidase; Humans; Lysine; Mutant Proteins; Parkinson Disease; Polyubiquitin; Protein Binding; Protein Processing, Post-Translational; Ubiquitin-Protein Ligases; Ubiquitination | 2010 |
Gaucher type 2 disease: identification of a novel transversion mutation in a French-Irish patient.
Topics: Aspartic Acid; Female; France; Gaucher Disease; Glucosylceramidase; Humans; Infant; Ireland; Lysine; Point Mutation; Proline; Tyrosine | 1998 |