Results 281 to 290 of about 1,010,620 (323)
Iron overload and liver function in patients with beta thalassemia major: A cross sectional study. [PDF]
Pak J Med SciFaruqi A +3 more
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Family Planning practices among the parents of beta thalassemia major patients in Makran division, Balochistan: A cross-sectional study. [PDF]
Pak J Med SciUzair +5 more
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Beta Thalassemia in Children: Established Approaches, Old Issues, New Non-Curative Therapies, and Perspectives on Healing. [PDF]
J Clin MedOriga R, Issa L.
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Knowledge, attitude and acceptance regarding bone marrow transplantation in caregivers of beta-thalassemia major patients. [PDF]
J Community GenetJayaram PR, Devadas S, Jain P, Devi C G.
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Beta-thalassemia Intermedia: An Overview
Pediatric Annals, 2008<P>Thalassemias are inherited anemias characterized by decreased or absent globin chain synthesis and by ineffective erythropoesis. They are classified according to the defective globin chain and to the clinical severity. Beta-thalassemias, which are prevalent in the Mediterranean region, have decreased or absent beta-globin chain synthesis ...
F. El Rassi +3 more
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Neurological complications of beta-thalassemia
Annals of Hematology, 2015The thalassemias are the most common single gene disorder in the world. Over the last years, several reports have demonstrated neurological complications in beta-thalassemia patients. In most cases, these complications remained subclinical and were detected only during neuropsychological, neurophysiological, or neuroimaging evaluation.
P. Nemtsas +4 more
semanticscholar +4 more sources