glycine has been researched along with Mucopolysaccharidoses in 5 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 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 (60.00) | 2.80 |
| Authors | Studies |
|---|---|
| Schlotawa, L | 3 |
| Adang, LA | 3 |
| Radhakrishnan, K | 2 |
| Ahrens-Nicklas, RC | 2 |
| Preiskorn, J | 1 |
| Ahrens-Nicklas, R | 1 |
| Schiller, S | 1 |
| Gärtner, J | 2 |
| Friede, T | 1 |
| Groeschel, S | 1 |
| Kehrer, C | 1 |
| Harzer, K | 1 |
| Staretz-Chacham, O | 1 |
| Silva, TO | 1 |
| Schwartz, IVD | 1 |
| De Castro, M | 1 |
| Costin, C | 1 |
| Montgomery, EF | 1 |
| Dierks, T | 1 |
| Brady, RO | 1 |
| Omenn, GS | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| The Myelin Disorders Biorepository Project and Global Leukodystrophy Initiative Clinical Trials Network[NCT03047369] | 12,000 participants (Anticipated) | Observational [Patient Registry] | 2016-12-08 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for glycine 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; Oxidoreduct | 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 | 2020 |
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter | 1976 |
2 other studies available for glycine 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; Le | 2020 |
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors | 1976 |