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Hemoglobin
international journal for hemoglobin research
Volume 38, 2014 - Issue 3
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Research Article

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

Chris AdhiyantoDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan;Faculty of Medicine and Health Science, Universitas Islam Negeri Syarif Hidayatullah JakartaIndonesiaCorrespondence[email protected] [email protected]
,
Yukio HattoriDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Yasuhiro YamashiroDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Ferania MellaDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Takenori NittaDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Mizuki IihoshiDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Satsuki ArakiDepartment of Health Science, Yamaguchi University Graduate School of Medicine UbeJapan
,
Maryam MatarUnited Arab Emirates Genetic Disease Association DubaiUnited Arab Emirates
&
Fumiya TakagiFukuyama Rihshou KK, Fukuyama Medical Center FukuyamaJapan
 show all
Pages 169-172 | Received 03 Mar 2013, Accepted 14 Nov 2013, Published online: 10 Mar 2014

Citations (7)

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Read on this site (4)

Xi Yao, Lu-Hong Xu, Hong-Gui Xu, Xin-Yu Li, Yong Liu & Jian-Pei Fang. (2019) Iron Metabolism and Oxidative Status in Patients with Hb H Disease. Hemoglobin 43:1, pages 38-41.
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Ferania Mella, Yasuhiro Yamashiro, Chris Adhiyanto, Tatehiko Tanaka, Takenori Nitta, Yuki Amao & Masafumi Kimoto. (2018) A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin. Hemoglobin 42:1, pages 1-6.
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Amira Abdel Moneam Adly, Nayera Hazaa Khalil ElSherif, Eman Abdel Rahman Ismail, Yosra Abdelzaher Ibrahim, Gamal Niazi & Sara Hamed Elmetwally. (2017) Ischemia-modified albumin as a marker of vascular dysfunction and subclinical atherosclerosis in β-thalassemia major. Redox Report 22:6, pages 430-438.
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Takenori Nitta, Fumio Kawano, Yasuhiro Yamashiro, Fumiya Takagi, Tomoaki Murata, Tatehiko Tanaka, Mella Ferania, Chris Adhiyanto & Yukio Hattori. (2015) A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor. Hemoglobin 39:2, pages 121-126.
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Articles from other publishers (3)

Debleena Basu, Debashree Guha Adhya, Rupal Sinha & Nishant Chakravorty. (2021) Role of malonaldehyde as a surrogate biomarker for iron overload in the β-thalassemia patient: A systematic meta-analysis. Advances in Redox Research 3, pages 100017.
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Husseen Manafikhi, Gregor Drummen, Maura Palmery & Ilaria Peluso. (2017) Total Antioxidant Capacity in beta-thalassemia: A systematic review and meta-analysis of case-control studies. Critical Reviews in Oncology/Hematology 110, pages 35-42.
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Semra Acer, Yasemin I Balcı, Gökhan Pekel, Tuğba T Ongun, Aziz Polat, Ebru N Çetin & Ramazan Yağcı. (2016) Retinal nerve fiber layer thickness and retinal vessel calibers in children with thalassemia minor. SAGE Open Medicine 4, pages 205031211666168.
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