porphobilinogen has been researched along with Thalassemia in 3 studies
Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (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 |
---|---|
FELDMAN, F | 1 |
LICHTMAN, HC | 1 |
Baĭtaeva, DA | 1 |
Abdullaev, GM | 1 |
Safarov, IuI | 1 |
Lyberatos, C | 1 |
Papadopoulos, N | 1 |
Papasteriadis, E | 1 |
Mitsiou, C | 1 |
Philippidou, A | 1 |
Gardikas, C | 1 |
3 other studies available for porphobilinogen and Thalassemia
Article | Year |
---|---|
IN VITRO PORPHOBILINOGEN AND PORPHYRIN SYNTHESIS IN THALASSEMIA MAJOR AND SICKLE CELL ANEMIA.
Topics: Amino Acid Oxidoreductases; Anemia; Anemia, Sickle Cell; beta-Thalassemia; Heme; In Vitro Techniques | 1964 |
[Porphyrin metabolic indices in the diagnosis of anemia in thalassemia].
Topics: Adolescent; Adult; Aminolevulinic Acid; Anemia; Child; Coproporphyrins; Erythrocytes; Female; Free R | 1982 |
Urine porphyrins and their precursors in homozygous beta-thalassaemia.
Topics: Adolescent; Adult; Aminolevulinic Acid; Child; Child, Preschool; Coproporphyrins; Female; Homozygote | 1975 |