n-formylglycine has been researched along with Mucopolysaccharidoses in 3 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 | 0 (0.00) | 24.3611 |
| 2020's | 3 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adang, LA; Ahrens-Nicklas, RC; Radhakrishnan, K; Schlotawa, L | 1 |
| Adang, LA; Ahrens-Nicklas, R; Friede, T; Gärtner, J; Preiskorn, J; Schiller, S; Schlotawa, L | 1 |
| Adang, LA; Ahrens-Nicklas, RC; Costin, C; De Castro, M; Dierks, T; Gärtner, J; Groeschel, S; Harzer, K; Kehrer, C; Montgomery, EF; Radhakrishnan, K; Schlotawa, L; Schwartz, IVD; Silva, TO; Staretz-Chacham, O | 1 |
2 review(s) available for n-formylglycine and Mucopolysaccharidoses
| Article | Year |
|---|---|
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
Topics: Glycine; Humans; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Mutation; Oxidoreductases Acting on Sulfur Group Donors; Protein Processing, Post-Translational; Sphingolipidoses; Sulfatases | 2020 |
A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency.
Topics: Glycine; Humans; Leukodystrophy, Metachromatic; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Oxidoreductases Acting on Sulfur Group Donors; Protein Processing, Post-Translational; Sulfatases | 2020 |
1 other study(ies) available for n-formylglycine and Mucopolysaccharidoses
| Article | Year |
|---|---|
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.
Topics: Adolescent; Child; Child, Preschool; Female; Genotype; Glycine; Humans; Infant; Internationality; Leukodystrophy, Metachromatic; Male; Mucopolysaccharidoses; Multiple Sulfatase Deficiency Disease; Mutation; Oxidoreductases Acting on Sulfur Group Donors; Phenotype; Rare Diseases; Retrospective Studies; Sulfatases | 2020 |