arginine has been researched along with alpha-Galactosidase A Deficiency in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Imai, H; Kitagawa, W; Komatsuda, A; Miura, N; Nishikawa, K; Suzuki, K; Suzuki, S; Watanabe, D | 1 |
| Roth, J; Yam, GH; Zuber, C | 1 |
| Holcenberg, JS | 1 |
| Batshaw, ML; Braine, H; Brusilow, SW; Moser, HW; Murray, C | 1 |
1 review(s) available for arginine and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
Progressive renal failure despite long-term biweekly enzyme replacement therapy in a patient with Fabry disease secondary to a new α-galactosidase mutation of Leu311Arg (L311R).
Topics: Adult; alpha-Galactosidase; Arginine; Biopsy; Disease Progression; DNA Mutational Analysis; Drug Administration Schedule; Enzyme Replacement Therapy; Fabry Disease; Glomerular Filtration Rate; Humans; Isoenzymes; Kidney; Leucine; Male; Mutation; Recombinant Proteins; Renal Insufficiency; Time Factors; Treatment Outcome | 2011 |
3 other study(ies) available for arginine and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
A synthetic chaperone corrects the trafficking defect and disease phenotype in a protein misfolding disorder.
Topics: 1-Deoxynojirimycin; alpha-Galactosidase; Amino Acid Substitution; Animals; Arginine; Cells, Cultured; Fabry Disease; Fibroblasts; Glutamine; Humans; Lysosomes; Mice; Mice, Transgenic; Molecular Chaperones; Mutation; Phenotype; Protein Binding; Protein Folding; Protein Transport; Trihexosylceramides | 2005 |
Enzyme therapy: problems and solutions.
Topics: Animals; Arginine; Blood Coagulation Disorders; Enzyme Therapy; Enzymes; Enzymes, Immobilized; Erwinia; Escherichia coli; Fabry Disease; Folic Acid; gamma-Glutamyl Hydrolase; Gaucher Disease; Humans; Hydrogen-Ion Concentration; Kinetics; Lysosomes; Metabolic Clearance Rate; Neoplasms; Poisoning; Ribonucleases; Urokinase-Type Plasminogen Activator | 1982 |
Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Benzoates; Carbamoyl-Phosphate Synthase (Ammonia); Dietary Proteins; Fabry Disease; Hippurates; Humans; Male; Nitrogen; Ornithine Carbamoyltransferase Deficiency Disease; Phytanic Acid; Plasmapheresis; Refsum Disease; Trihexosylceramides; Urea | 1979 |