Plasma homocysteine levels in patients with β‐thalassaemia major
Author:
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/00365510701516343
Reference44 articles.
1. Complications of β-thalassemia major in North America
2. Pathophysiology of β Thalassemia—A Guide to Molecular Therapies
3. NEW INSIGHTS INTO ERYTHROPOIESIS: The Roles of Folate, Vitamin B12, and Iron
4. Significance of subnormal red-cell folate in thalassaemia.
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1. Nutritional Status in a Sample of Patients With β-Thalassemia Major;Cureus;2022-08-14
2. 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;2020-05
Effects of Alpha-Lipoic Acid Supplementation on Cardiovascular Disease Risk Factors in β-Thalassemia Major Patients: A Clinical Trial Crossover Study
3. Study of Serum Homocysteine Level Variations in Sickle Cell Disease: A Meta-analysis Study;Indian journal of Medical Biochemistry;2020
4. The relationship between ferritin levels and oxidative stress parameters in serum of β-thalassemia major patients;Archives of Biochemistry and Biophysics;2018-12
5. Assessment of Serum Folic Acid and Homocysteine in Thalassemia Major Patients Before and After Folic Acid Supplement Cessation;Journal of Pediatric Hematology/Oncology;2018-10
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