glycine has been researched along with Peroxisomal Disorders in 1 studies
Peroxisomal Disorders: A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Gärtner, J | 1 |
| Preuss, N | 1 |
| Brosius, U | 1 |
| Biermanns, M | 1 |
1 other study available for glycine and Peroxisomal Disorders
| Article | Year |
|---|---|
Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype.
Topics: Aspartic Acid; ATPases Associated with Diverse Cellular Activities; Child; Glycine; Humans; Infant; | 1999 |