acetylglucosamine has been researched along with Diseases in Twins in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Jaeken, J | 1 |
| Chitayat, D; Goldman, HS; Hahm, SY; Marion, RW; Nakagawa, S; Sachs, GS | 1 |
2 other study(ies) available for acetylglucosamine and Diseases in Twins
| Article | Year |
|---|---|
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins].
Topics: Acetylglucosamine; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Demyelinating Diseases; Diseases in Twins; Female; Galactose; Glucosamine; Humans; Intellectual Disability; Sialic Acids; Syndrome; Twins, Monozygotic | 1989 |
Aspartylglucosaminuria in a Puerto Rican family: additional features of a panethnic disorder.
Topics: Acetylglucosamine; Adolescent; Amidohydrolases; Aspartylglucosylaminase; Consanguinity; Diseases in Twins; Genes, Recessive; Gonadal Dysgenesis; Humans; Male; Pedigree; Puerto Rico; Spondylolisthesis; Spondylolysis; Testis | 1988 |