lysine has been researched along with Fabry Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Kajita, M; Miyazaki, T; Mizutani, N; Murata, Y; Niwa, T; Ohmori, S; Seo, H | 1 |
| Gardner, LI | 1 |
1 review(s) available for lysine and Fabry Disease
| 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 |
1 other study(ies) available for lysine and Fabry Disease
| Article | Year |
|---|---|
A novel mutation (E358K) in the alpha-galactosidase A gene detected in a Japanese family with Fabry disease.
Topics: Adolescent; Adult; alpha-Galactosidase; Amino Acid Substitution; Base Sequence; DNA; DNA Mutational Analysis; Fabry Disease; Family Health; Female; Glutamic Acid; Humans; Japan; Lysine; Male; Mutation; Pedigree; Point Mutation | 1998 |