methionine has been researched along with Anemia, Congenital Nonspherocytic Hemolytic in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aydinok, Y; Manco, L; Ozer, E; Serdaroglu, G; Yilmaz, S | 1 |
| Carreras, J; Climent, F; Corrons, JL; Ramirez Bajo, MJ; Repiso, A | 1 |
2 other study(ies) available for methionine and Anemia, Congenital Nonspherocytic Hemolytic
| Article | Year |
|---|---|
Triosephosphate isomerase deficiency: a patient with Val231Met mutation.
Topics: Adolescent; Amino Acid Substitution; Anemia, Hemolytic, Congenital Nonspherocytic; Humans; Male; Methionine; Triose-Phosphate Isomerase; Valine | 2011 |
Phosphoglycerate mutase BB isoenzyme deficiency in a patient with non-spherocytic anemia: familial and metabolic studies.
Topics: Adult; Anemia, Hemolytic, Congenital Nonspherocytic; DNA, Complementary; Erythrocytes; Family Health; Female; Homozygote; Humans; Isoleucine; Methionine; Mutation; Phosphoglycerate Mutase; Phosphoric Monoester Hydrolases; Point Mutation; Protein Isoforms | 2005 |