Page last updated: 2024-10-20

porphobilinogen and Thalassemia

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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19903 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
FELDMAN, F1
LICHTMAN, HC1
Baĭtaeva, DA1
Abdullaev, GM1
Safarov, IuI1
Lyberatos, C1
Papadopoulos, N1
Papasteriadis, E1
Mitsiou, C1
Philippidou, A1
Gardikas, C1

Other Studies

3 other studies available for porphobilinogen and Thalassemia

ArticleYear
IN VITRO PORPHOBILINOGEN AND PORPHYRIN SYNTHESIS IN THALASSEMIA MAJOR AND SICKLE CELL ANEMIA.
    Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119

    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].
    Vrachebnoe delo, 1982, Issue:1

    Topics: Adolescent; Adult; Aminolevulinic Acid; Anemia; Child; Coproporphyrins; Erythrocytes; Female; Free R

1982
Urine porphyrins and their precursors in homozygous beta-thalassaemia.
    Acta haematologica, 1975, Volume: 54, Issue:2

    Topics: Adolescent; Adult; Aminolevulinic Acid; Child; Child, Preschool; Coproporphyrins; Female; Homozygote

1975