pyridoxal has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Merx, J | 1 |
| van Outersterp, RE | 1 |
| Engelke, UFH | 1 |
| Hendriks, V | 1 |
| Wevers, RA | 1 |
| Huigen, MCDG | 1 |
| Waterval, HWAH | 1 |
| Körver-Keularts, IMLW | 1 |
| Mecinović, J | 1 |
| Rutjes, FPJT | 1 |
| Oomens, J | 1 |
| Coene, KLM | 1 |
| Martens, J | 1 |
| Boltje, TJ | 1 |
| Bisello, G | 1 |
| Bertoldi, M | 1 |
| Tabolin, VA | 1 |
| Kruglov, BV | 1 |
| Lebedev, VP | 1 |
| Levitina, NO | 1 |
2 reviews available for pyridoxal and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Compound Heterozygosis in AADC Deficiency and Its Complex Phenotype in Terms of AADC Protein Population.
Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Carboxy-Lyases; Phenotyp | 2022 |
[Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Carboxy-Lyases; Child; Child, Preschool; Diabetes | 1972 |
1 other study available for pyridoxal and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Identification of Δ-1-pyrroline-5-carboxylate derived biomarkers for hyperprolinemia type II.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Biomarkers; Phosphate | 2022 |