Page last updated: 2024-10-30

mechlorethamine and Thalassemia

mechlorethamine has been researched along with Thalassemia in 1 studies

nitrogen mustard : Compounds having two beta-haloalkyl groups bound to a nitrogen atom, as in (X-CH2-CH2)2NR.

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 (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (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
Cech, P1
Testa, U1
Dubart, A1
Schneider, P1
Bachmann, F1
Guerrasio, A1
Beuzard, Y1
Schmidt, PM1
Clément, F1
Rosa, J1

Other Studies

1 other study available for mechlorethamine and Thalassemia

ArticleYear
Lasting Hb F reactivation and Hb A2 reduction induced by the treatment of Hodgkin's disease in a woman heterozygous for beta-thalassemia and the Swiss type of the heterocellular hereditary persistence of Hb F.
    Acta haematologica, 1982, Volume: 67, Issue:4

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Female; Fetal Hemoglobin; Globins; Hemoglobin

1982