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Scandinavian Journal of Clinical and Laboratory Investigation Volume 68, 2008 - Issue 2
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Original Article

Plasma homocysteine levels in patients with β‐thalassaemia major

S. Ozdem Akdeniz University, School of Medicine
,
A. Kupesiz Department of Central Laboratory Clinical Biochemistry Unit
&
A. Yesilipek Department of Pediatric Hematology and Oncology, Antalya, Turkey
Pages 134-139 | Received 26 Mar 2007, Accepted 02 Jun 2007, Published online: 08 Jul 2009

Citations (12)

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Khadijeh Jamshidi, Hadi Abdollahzad, Mostafa Nachvak, Mansour Rezaei, Mohammad Reza Golpayegani & Elham Sharifi Zahabi. (2020) Effects of Alpha-Lipoic Acid Supplementation on Cardiovascular Disease Risk Factors in β-Thalassemia Major Patients: A Clinical Trial Crossover Study. Journal of Blood Medicine 11, pages 131-139.
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Khodayar Ghorban, Mehrnoosh Shanaki, Naser Mobarra, Mehdi Azad, Jahanbakhsh Asadi, Reza Pakzad & Hassan Ehteram. (2016) Apolipoproteins A1, B, and other prognostic biochemical cardiovascular risk factors in patients with beta-thalassemia major. Hematology 21:2, pages 113-120.
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Articles from other publishers (10)

Irene Lidoriki, George Stavrou, Dimitrios Schizas, Maximos Frountzas, Lampros Fotis, Alkistis Kapelouzou, Smaro Kokkota, Barbara Fyntanidou & Katerina Kotzampassi. (2022) Nutritional Status in a Sample of Patients With β-Thalassemia Major. Cureus.
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Shekhar B Padhyegurjar, Prashant Hisalkar, Chandrakant G Kamble, Jagdish D Powar & Bhausaheb V Jagdale. (2020) Study of Serum Homocysteine Level Variations in Sickle Cell Disease: A Meta-analysis Study. Indian Journal of Medical Biochemistry 24:3, pages 104-114.
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Ziya Salman, Tamer Yılmaz & Güldal Mehmetçik. (2018) The relationship between ferritin levels and oxidative stress parameters in serum of β-thalassemia major patients. Archives of Biochemistry and Biophysics 659, pages 42-46.
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Adel Baghersalimi, Hajar Hemmati Kolachahi, Bahram Darbandi, Zahra Kamran Mavardiani, Maryam Alizadeh Alinodehi, Setila Dalili & Afagh Hassanzadeh Rad. (2018) Assessment of Serum Folic Acid and Homocysteine in Thalassemia Major Patients Before and After Folic Acid Supplement Cessation. Journal of Pediatric Hematology/Oncology 40:7, pages 504-507.
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Meng-Yao Lu, Ting-Hao LinPo-Hung ChiangPei-Hsin KuoNing WangWen-Hsin WuKai-Hsin Lin & Tzu-Hua Wu. (2017) Deferasirox–Iron Complex Formation Ratio as an Indicator of Long-term Chelation Efficacy in β-Thalassemia Major. Therapeutic Drug Monitoring 39:2, pages 185-191.
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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.
Crossref
Mai A. Abd-Elmawla, Sherine M. Rizk, Ilham Youssry & Amira A. Shaheen. (2016) Impact of Genetic Polymorphism of methylenetetrahydrofolate reductase C677T on Development of Hyperhomocysteinemia and Related Oxidative Changes in Egyptian β-Thalassemia Major Patients. PLOS ONE 11:5, pages e0155070.
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Orhan Gursel, Ahmet E. Kurekci, Emre Tascilar, Talia Ileri, Demet Altun, Serkan Tapan, Ismail Kurt, Murat Kocaoglu, Ahmet Aydin, Vedat Okutan & Okan Ozcan. (2012) Premature Atherosclerosis in Children With β-Thalassemia Major. Journal of Pediatric Hematology/Oncology 34:8, pages 630-634.
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Viroj Wiwanitkit. (2011) Narrowband ultraviolet B phototherapy and serum folic acid level. Lasers in Medical Science 27:3, pages 685-685.
Crossref
Ellen B Fung. (2010) Nutritional deficiencies in patients with thalassemia. Annals of the New York Academy of Sciences 1202:1, pages 188-196.
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