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vanilmandelic acid and Thalassemia

vanilmandelic acid has been researched along with Thalassemia in 1 studies

Vanilmandelic Acid: A 3-O-methyl ether of 3,4-dihydroxymandelic acid. It is an end-stage metabolite of CATECHOLAMINES; EPINEPHRINE; and NOREPINEPHRINE.
vanillylmandelic acid : An aromatic ether that is the 3-O-methyl ether of 3,4-dihydroxymandelic acid.

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
Thirawarapan, SS1
Snongchart, N1
Fucharoen, S1
Tanphaichitr, VS1
Dhorranintra, B1

Other Studies

1 other study available for vanilmandelic acid and Thalassemia

ArticleYear
Study of mechanisms of post-transfusion hypertension in thalassaemic patients.
    The Southeast Asian journal of tropical medicine and public health, 1989, Volume: 20, Issue:3

    Topics: Adolescent; Adult; Blood Viscosity; Child; Child, Preschool; Female; Furosemide; Hematocrit; Humans;

1989