Protein C and Protein S: Causative factor for developing a hemorrhagic infarct in a HbE/Beta thalassemia child
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-009-0297-5.pdf
Reference12 articles.
1. Rees DC, Styles L, Vichinsky EP, Clegg JB, Weatherall DJ. The hemoglobin E syndromes. Ann N Y Acad Sci 1998; 850: 334–343.
2. Capellini MD, Robbiolo L, Bottasso BM, Cappola R, Fiorelli G et al. Venus Thromboembolism and hypercoagulability in splenectomized patients with thalassemia intermedia. Br J Hematol 2000; 111: 467–473.
3. Logothetis J, Constantoulakis M, Economidou J, Stefanis C, Hakas P, Augoustaki O et al. Thalassemia major: A survey of 138 cases with emphasis on neurological and muscular aspects. Neurology 1972; 22: 294–304.
4. Borgna Pignatti C, Carnelli V, Caruso V et al. Thromboembolic events in beta thalassemia major: an Italian multicenter study. Acta Haematol 1998; 99: 76–79.
5. Paolino E, Monetti VC, Granieri E, Boldrini. Acute cerebrovascular insults in homozygous beta-thalassaemia: a case report. J Neurol 1983; 230: 37–41.
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1. Protein C and Protein S Levels in β-Thalassemia Major Patients in Erbil, Kurdistan Region;Cellular and Molecular Biology;2020-07-31
2. Hemoglobinopathies and Stroke: Strategies for Prevention and Treatment;Current Treatment Options in Cardiovascular Medicine;2012-03-06
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