imidazole has been researched along with Tay-Sachs Disease in 2 studies
imidazole: RN given refers to parent cpd
1H-imidazole : An imidazole tautomer which has the migrating hydrogen at position 1.
Tay-Sachs Disease: An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry.
| 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 |
|---|---|
| BESSMAN, SP | 2 |
| BALDWIN, R | 1 |
2 other studies available for imidazole and Tay-Sachs Disease
| Article | Year |
|---|---|
Imidazole aminoaciduria in cerebromacular degeneration.
Topics: Amino Acids; Body Fluids; Histidine; Humans; Imidazoles; Lipidoses; Methylhistidines; Tay-Sachs Dise | 1962 |
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 |