phenylalanine has been researched along with Glucosephosphate Dehydrogenase Deficiency in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| He, F; Wang, W; Wang, Z; Zhong, K | 1 |
| Wachtel, U | 1 |
| Danks, DM | 1 |
1 review(s) available for phenylalanine and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe.
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Biopterins; Diet; Dietary Proteins; Dihydropteridine Reductase; Europe; Female; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant; Infant, Newborn; Intellectual Disability; Liver; Mass Screening; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pregnancy; Pregnancy Complications; Prognosis; Pterins; Tyrosine | 1986 |
2 other study(ies) available for phenylalanine and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Neonatal screening external quality assessment in China, 2014.
Topics: 17-alpha-Hydroxyprogesterone; China; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Neonatal Screening; Phenylalanine; Quality Assurance, Health Care; Thyrotropin | 2015 |
Inborn errors of metabolism. Variability within single diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Genes; Genetic Variation; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Mutation; Phenylalanine; Phenylketonurias | 1971 |