acetylglucosamine has been researched along with Fabry Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chabás, A; Coll, MJ; Fernández-Herrera, JM; García-Díez, A; Sánchez-Pérez, J; Vargas-Díez, E | 1 |
| Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 1 |
| Cooper, A; Forsyth, JM; Guy, R; Morton, RE | 1 |
1 review(s) available for acetylglucosamine and Fabry Disease
| Article | Year |
|---|---|
Angiokeratoma corporis diffusum in a Spanish patient with aspartylglucosaminuria.
Topics: Acetylglucosamine; Adult; Aspartylglucosaminuria; Disease Progression; Fabry Disease; Female; Follow-Up Studies; Humans; Macroglossia; Skin Diseases, Genetic | 2002 |
2 other study(ies) available for acetylglucosamine and Fabry Disease
| Article | Year |
|---|---|
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull | 1981 |
Co-existence of lysosomal storage diseases in a consanguineous family.
Topics: Acetylglucosamine; Asia; Child, Preschool; Consanguinity; England; Fabry Disease; Female; Heterozygote; Humans; Infant, Newborn; Lysosomal Storage Diseases; Male; Pedigree | 2001 |