Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50)-Reference-Cited by-同舟云学术

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Oxidation Status of β-Thalassemia Minor and Hb H Disease, and Its Association with Glycerol Lysis Time (GLT50)

Published:2014-03-10 Issue:3 Volume:38 Page:169-172
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Adhiyanto Chris,Hattori Yukio,Yamashiro Yasuhiro,Mella Ferania,Nitta Takenori,Iihoshi Mizuki,Araki Satsuki,Matar Maryam,Takagi Fumiya

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.892884

Reference23 articles.

1. Redox-Genome Interactions in Health and Disease

2. Monitoring of oxidative free radical damage in vivo: Analytical aspects

3. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes

4. The role of oxidant injury in the pathophysiology of human thalassemias

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1. Role of malonaldehyde as a surrogate biomarker for iron overload in the β-thalassemia patient: A systematic meta-analysis;Advances in Redox Research;2021-12

2. Iron Metabolism and Oxidative Status in Patients with Hb H Disease;Hemoglobin;2019-01-02

3. A Coincidental Discovery of a New Stable Variant (Hb Hachioji orHBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin;Hemoglobin;2018-01-02

4. Ischemia-modified albumin as a marker of vascular dysfunction and subclinical atherosclerosis in β-thalassemia major;Redox Report;2017-03-13

5. Total Antioxidant Capacity in beta-thalassemia: A systematic review and meta-analysis of case-control studies;Critical Reviews in Oncology/Hematology;2017-02

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