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pyridoxine 5-phosphate and Thalassemia

pyridoxine 5-phosphate has been researched along with Thalassemia in 1 studies

pyridoxine 5-phosphate: RN given refers to parent cpd

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 Excerpts

ExcerptRelevanceReference
"When G6PD deficiency occurs with heterozygous beta-thalassaemia, GR is usually saturated with FAD as in G6PD deficiency alone, unless there is an inherited, very slow red-cell metabolism of riboflavin to FMN."1.27Glutathione reductase activity and its relationship to pyridoxine phosphate activity in G6PD deficiency. ( Anderson, BB; Clements, JE; Perry, GM; Salsini, G; Studds, C; Vullo, C, 1987)

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
Anderson, BB1
Clements, JE1
Perry, GM1
Studds, C1
Vullo, C1
Salsini, G1

Other Studies

1 other study available for pyridoxine 5-phosphate and Thalassemia

ArticleYear
Glutathione reductase activity and its relationship to pyridoxine phosphate activity in G6PD deficiency.
    European journal of haematology, 1987, Volume: 38, Issue:1

    Topics: Erythrocytes; Flavin Mononucleotide; Flavin-Adenine Dinucleotide; Flavoproteins; Glucosephosphate De

1987