4-nitrocatechol sulfate has been researched along with Mucopolysaccharidoses in 1 studies
*Mucopolysaccharidoses: Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alves, S; Coutinho, MF; Gupta, AK; Kapoor, S; Mishra, OP; Prasad, R; Sharma, A; Singh, A | 1 |
1 other study(ies) available for 4-nitrocatechol sulfate and Mucopolysaccharidoses
| Article | Year |
|---|---|
I Cell Disease (Mucolipidosis II Alpha/Beta): From Screening to Molecular Diagnosis.
Topics: Catechols; Diagnosis, Differential; Humans; Infant; Male; Mucolipidoses; Mucopolysaccharidoses; Phenotype | 2017 |