Treatment of β-Thalassemia/Hemoglobin E with Antioxidant Cocktails Results in Decreased Oxidative Stress, Increased Hemoglobin Concentration, and Improvement of the Hypercoagulable State

scientific article published on 19 May 2015

Treatment of β-Thalassemia/Hemoglobin E with Antioxidant Cocktails Results in Decreased Oxidative Stress, Increased Hemoglobin Concentration, and Improvement of the Hypercoagulable State is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1155/2015/537954
P932PMC publication ID4452506
P698PubMed publication ID26078808
P5875ResearchGate publication ID277930060

P50authorSomdet SrichairatanakoolQ56806566
P2093author name stringSuthat Fucharoen
Noppadol Siritanaratkul
Narumol Panichkul
Ratiya Charoensakdi
Ruchaneekorn W Kalpravidh
Suneerat Hatairaktham
Orn-uma Yanpanitch
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Curcumin, a cancer chemopreventive and chemotherapeutic agent, is a biologically active iron chelatorQ24652363
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Detection of PF3 availability in whole blood from volunteers and beta-thalassemia/HbE patients: a promising method for prediction of thrombotic tendencyQ41080863
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Vitamin E supplementation reduces oxidative stress in beta thalassaemia intermedia.Q42449492
Labile plasma iron (LPI) as an indicator of chelatable plasma redox activity in iron-overloaded beta-thalassemia/HbE patients treated with an oral chelatorQ42461969
Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in beta-thalassemia intermedia patientsQ42505009
Improvement in oxidative stress and antioxidant parameters in beta-thalassemia/Hb E patients treated with curcuminoidsQ43245550
Antioxidant defense status of red blood cells of patients with beta-thalassemia and Ebeta-thalassemiaQ43542984
Immunosuppressive therapy regimen and platelet activation in renal transplant patientsQ44184230
Clinical trial of deferiprone iron chelation therapy in beta-thalassaemia/haemoglobin E patients in ThailandQ44503973
Effect of sulfur amino acids on stimulus-induced superoxide generation and translocation of p47phox and p67phox to cell membrane in human neutrophils and the scavenging of free radicalQ45255621
Combined therapy of silymarin and desferrioxamine in patients with beta-thalassemia major: a randomized double-blind clinical trial.Q46005571
Effect of antioxidant therapy on hepatic fibrosis and liver iron concentrations in β-thalassemia major patients.Q46364415
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Deferiprone (GPO-L-ONE(®) ) monotherapy reduces iron overload in transfusion-dependent thalassemias: 1-year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO-L-ONE; A001) from Thailand.Q53995645
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How much vitamin E? ... Just enough!Q55042686
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In-vivo platelet activation correlates with red cell anionic phospholipid exposure in patients with beta-thalassaemia majorQ73535703
Inhibitory effect of curcumin, a food spice from turmeric, on platelet-activating factor- and arachidonic acid-mediated platelet aggregation through inhibition of thromboxane formation and Ca2+ signalingQ78251657
SYNTHESIS OF DIACETYLDICHLOROFLUORESCIN: A STABLE REAGENT FOR FLUOROMETRIC ANALYSISQ78493010
Effect of coenzyme Q10 as an antioxidant in beta-thalassemia/Hb E patientsQ80013105
Vitamin E inhibition on platelet procoagulant activity: involvement of aminophospholipid translocase activityQ83375709
P275copyright licenseCreative Commons Attribution 3.0 UnportedQ14947546
P6216copyright statuscopyrightedQ50423863
P304page(s)537954
P577publication date2015-05-19
P1433published inOxidative medicine and cellular longevityQ26840015
P1476titleTreatment of β-Thalassemia/Hemoglobin E with Antioxidant Cocktails Results in Decreased Oxidative Stress, Increased Hemoglobin Concentration, and Improvement of the Hypercoagulable State
P478volume2015

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cites work (P2860)
Q33761211European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS).
Q36138738HbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics
Q46460675Ischemia-modified albumin as a marker of vascular dysfunction and subclinical atherosclerosis in β-thalassemia major.

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