phenylalanine has been researched along with Anemia, Hemolytic, Congenital in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (100.00) | 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 | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dacie, JV; Gaffney, PJ; Lehmann, H; Shinton, NK | 1 |
Matsuoka, M; Miyaji, T; Numakura, H; Ohba, Y; Yokoyama, M | 1 |
Bratu, V; Lehmann, H; Lorkin, PA; Predescu, C | 1 |
Bianco, G; Gallo, E; Lehmann, H; Mazza, U; Prato, V; Ricco, G | 1 |
Clegg, JB; Oski, FA; Rieder, RF | 1 |
5 other study(ies) available for phenylalanine and Anemia, Hemolytic, Congenital
Article | Year |
---|---|
Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser).
Topics: Amino Acid Sequence; Anemia, Hemolytic, Congenital; Chromatography, Paper; Electrophoresis; Heinz Bodies; Hemoglobins, Abnormal; Humans; Infant, Newborn; Mutation; Paper; Phenylalanine; Serine | 1967 |
Hemoglobin Hirosaki (alpha 43 [CE 1] Phe replaced by Leu), a new unstable variant.
Topics: Amino Acid Sequence; Anemia, Hemolytic, Congenital; Drug Stability; Female; Genetic Variation; Hemoglobins, Abnormal; Hot Temperature; Humans; Japan; Leucine; Male; Pedigree; Phenylalanine; Solubility | 1975 |
Haemoglobin Buccureşti 42(CD1) Phe-Leu, a cause of unstable haemoglobin haemolytic anaemia.
Topics: Adolescent; Adult; Amino Acid Sequence; Amino Acids; Anemia, Hemolytic, Congenital; Bilirubin; Chemical Precipitation; Chromatography, Ion Exchange; Drug Stability; Erythrocyte Count; Female; Globins; Hemoglobins, Abnormal; Hot Temperature; Humans; Leucine; Oxygen; Peptides; Phenylalanine; Protein Binding; Romania; Trypsin | 1971 |
Haemolytic anaemia due to haemoglobin Torino.
Topics: Adolescent; Adult; Aged; Anemia, Hemolytic, Congenital; Child; Erythrocytes; Female; Genes, Dominant; Hemoglobins, Abnormal; Humans; Male; Phenylalanine; Porphyrins; Pyrroles; Splenectomy; Sulfonamides; Valine | 1970 |
Hemoglobin Philly (beta 35 tyrosine phenylalanine): studies in the molecular pathology of hemoglobin.
Topics: Amino Acids; Anemia, Hemolytic, Congenital; Child; Chromatography; Culture Techniques; Electrophoresis; Erythrocytes; Female; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Mutation; Phenylalanine; Spectrophotometry; Sulfhydryl Compounds; Tyrosine; Ultracentrifugation | 1969 |