arginine has been researched along with Oxaluria, Primary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fillaus, JA; Plumb, TJ; Swee, ML | 1 |
| Abramowicz, D; Acquaviva, C; Cochat, P; Durrbach, A; Fargue, S; Gagnadoux, MF; Girardin, E; Harambat, J; Janssen, F; Legendre, C; Liutkus, A; Macher, MA; Mourani, C; Nivet, H; Rolland, MO; Schott, AM; Tsimaratos, M | 1 |
| Danpure, CJ; Leiper, JM; Oatey, PB | 1 |
1 review(s) available for arginine and Oxaluria, Primary
| Article | Year |
|---|---|
Nocturnal home hemodialysis for a patient with type 1 hyperoxaluria.
Topics: Adult; Amino Acid Substitution; Arginine; Circadian Rhythm; Combined Modality Therapy; DNA Mutational Analysis; Exons; Female; Glycine; Hemodialysis, Home; Humans; Hyperoxaluria, Primary; Kidney Failure, Chronic; Oxalates; Pyridoxine; Transaminases | 2013 |
2 other study(ies) available for arginine and Oxaluria, Primary
| Article | Year |
|---|---|
Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.
Topics: Amino Acid Substitution; Arginine; Child; Child, Preschool; Cohort Studies; Genotype; Heterozygote; Homozygote; Humans; Hyperoxaluria, Primary; Infant; Kidney Failure, Chronic; Mutation; Phenotype; Prognosis; Retrospective Studies; Transaminases | 2010 |
Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.
Topics: Alanine Transaminase; Animals; Arginine; Biological Transport; COS Cells; Dimerization; Glycine; Humans; Hyperoxaluria, Primary; Leucine; Liver; Microbodies; Mitochondria; Point Mutation; Polymorphism, Genetic; Proline; Transaminases | 1996 |