glycine has been researched along with Hyperargininemia in 2 studies
Hyperargininemia: A rare autosomal recessive disorder of the urea cycle. It is caused by a deficiency of the hepatic enzyme ARGINASE. Arginine is elevated in the blood and cerebrospinal fluid, and periodic HYPERAMMONEMIA may occur. Disease onset is usually in infancy or early childhood. Clinical manifestations include seizures, microcephaly, progressive mental impairment, hypotonia, ataxia, spastic diplegia, and quadriparesis. (From Hum Genet 1993 Mar;91(1):1-5; Menkes, Textbook of Child Neurology, 5th ed, p51)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Amayreh, W | 1 |
| Meyer, U | 1 |
| Das, AM | 1 |
| Marescau, B | 1 |
| Lowenthal, A | 1 |
| Terheggen, HG | 1 |
| Esmans, E | 1 |
| Alderweireldt, F | 1 |
2 other studies available for glycine and Hyperargininemia
| Article | Year |
|---|---|
Treatment of arginase deficiency revisited: guanidinoacetate as a therapeutic target and biomarker for therapeutic monitoring.
Topics: Benzoates; Biomarkers; Child; Creatine; Glycine; Humans; Hyperargininemia; Male; Ornithine; Treatmen | 2014 |
Guanidino compounds in hyperargininemia.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography, Liquid; Chromatography, Thin Layer; | 1982 |