imidazole has been researched along with Gangliosidoses, GM2 in 1 studies
imidazole: RN given refers to parent cpd
1H-imidazole : An imidazole tautomer which has the migrating hydrogen at position 1.
Gangliosidoses, GM2: A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| BESSMAN, SP | 1 |
1 other study available for imidazole and Gangliosidoses, GM2
| Article | Year |
|---|---|
IMIDAZOLE AMINO ACIDURIA. A BIOCHEMICAL DEFECT IN JUVENILE TAY-SACHS DISEASE.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Gangliosidoses, GM2; Genetics, Medical; His | 1964 |