glycine has been researched along with Orphan Diseases in 2 studies
Orphan Diseases: Rare diseases that have not been well studied.
| Excerpt | Relevance | Reference |
|---|---|---|
| "His glycine index was 0." | 1.34 | Neonatal nonketotic hyperglycinemia. ( Bhamkar, RP; Colaco, P, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adang, LA | 1 |
| Schlotawa, L | 1 |
| Groeschel, S | 1 |
| Kehrer, C | 1 |
| Harzer, K | 1 |
| Staretz-Chacham, O | 1 |
| Silva, TO | 1 |
| Schwartz, IVD | 1 |
| Gärtner, J | 1 |
| De Castro, M | 1 |
| Costin, C | 1 |
| Montgomery, EF | 1 |
| Dierks, T | 1 |
| Radhakrishnan, K | 1 |
| Ahrens-Nicklas, RC | 1 |
| Bhamkar, RP | 1 |
| Colaco, P | 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] | |||||||
2 other studies available for glycine and Orphan Diseases
| 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 |
Neonatal nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Disease Progression; Fatal Outcome; Glycine; Humans; Hyperglyc | 2007 |